Enhancers that have rs566990143[chr11:78798362]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr11 78796204 78806518 enh28906
chr11 78798308 78798462 vista11049

Transcript factors that have rs566990143[chr11:78798362]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr11 78798123 78798699 ZBTB33 ENCODE Uniform TFBS no Lung (A549) 107992962
chr11 78798149 78799468 ZBTB33 GTRD no Lung (A549) 107992963
chr11 78798158 78798662 ZBTB33 ENCODE Uniform TFBS no Lung (A549) 107992964
chr11 78798159 78798599 ZNF274 ENCODE Uniform TFBS no Liver (HepG2) 107992965
chr11 78798163 78798599 ZBTB33 ENCODE Uniform TFBS no Lung (A549) 107992966
chr11 78798164 78799358 ZNF274 GTRD no Bone Marrow (K562) 107992967
chr11 78798167 78798577 ZBTB33 ENCODE Uniform TFBS no Lung (A549) 107992968
chr11 78798176 78798660 ZBTB33 ENCODE Uniform TFBS no Lung (A549) 107992969
chr11 78798179 78798663 ZBTB33 ENCODE Uniform TFBS no Lung (A549) 107992970
chr11 78798185 78799200 ZBTB33 GTRD no Lung (A549) 107992971
chr11 78798196 78799372 ZNF143 GTRD no Epithelial (MCF-7) 107992972
chr11 78798200 78798887 ZNF143 GTRD no Epithelial (MCF-7) 107992973
chr11 78798213 78799171 ZNF274 GTRD no Blood (GM12878) 107992974
chr11 78798217 78798586 EP300 UCSC Txn Factor no Conserved 107992975
chr11 78798217 78798586 ZBTB33 ENCODE Uniform TFBS no Lung (A549) 107992976
chr11 78798217 78798634 TCF12 UCSC Txn Factor no Conserved 107992977
chr11 78798217 78798634 ZBTB33 ENCODE Uniform TFBS no Lung (A549) 107992978
chr11 78798218 78798574 TAF1 ENCODE Uniform TFBS no Brain (SK-N-SH) 21506222
chr11 78798218 78798574 TAF1 ENCODE Uniform TFBS no Brain (SK-N-SH) 107992979
chr11 78798223 78798743 ZBTB33 ENCODE Uniform TFBS no Lung (A549) 107992980
chr11 78798225 78798605 ZNF274 ENCODE Uniform TFBS no Liver (HepG2) 107992981
chr11 78798230 78798554 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 107992982
chr11 78798231 78799349 ZNF143 GTRD no Epithelial (MCF-7) 107992983
chr11 78798235 78799139 ZNF274 GTRD no Blood (GM12878) 107992984
chr11 78798244 78798560 TAF1 ENCODE Uniform TFBS no Brain (SK-N-SH) 21506223
chr11 78798244 78798560 TAF1 ENCODE Uniform TFBS no Brain (SK-N-SH) 107992985
chr11 78798255 78799193 ZNF274 GTRD no Bone Marrow (K562) 107992986
chr11 78798265 78798933 ZNF274 GTRD no Bone Marrow (K562) 107992987
chr11 78798279 78798535 TAF1 ENCODE Uniform TFBS no Brain (SK-N-SH) 21506224
chr11 78798279 78798535 TAF1 ENCODE Uniform TFBS no Brain (SK-N-SH) 107992988
chr11 78798281 78799228 ZNF274 GTRD no Bone Marrow (K562) 107992989
chr11 78798282 78798526 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 107992990
chr11 78798288 78798548 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 107992991
chr11 78798302 78799346 ZBTB33 GTRD no Lung (A549) 107992992
chr11 78798330 78799371 ZNF143 GTRD no Epithelial (MCF-7) 107992993
chr11 78798331 78798641 TAF1 ENCODE Uniform TFBS no Brain (SK-N-SH) 21506225
chr11 78798331 78798641 TAF1 ENCODE Uniform TFBS no Brain (SK-N-SH) 107992994
chr11 78798336 78799193 ZNF143 GTRD no Epithelial (MCF-7) 107992995
chr11 78798343 78799305 ZNF274 GTRD no Blood (GM12878) 107992996
chr11 78798347 78799168 ZNF274 GTRD no Liver (HepG2) 107992997
chr11 78798351 78798364 SMAD2 JASPAR yes 40066294
chr11 78798351 78798364 SMAD2 JASPAR yes 114107742
chr11 78798358 78798371 ELF1 JASPAR yes 40066295
chr11 78798358 78798371 ELF1 JASPAR yes 114107743
chr11 78798359 78798372 ELF3 JASPAR yes 40066296
chr11 78798359 78798372 ELF3 JASPAR yes 114107744
chr11 78798360 78798371 ELF5 JASPAR yes 40066297
chr11 78798360 78798371 ELF5 JASPAR yes 114107745
chr11 78798360 78799320 ZNF274 GTRD no Cervix (HeLa-S3) 107992998
chr11 78798362 78798367 ETS2 TRANSFAC yes 40066298
chr11 78798362 78798367 ETS2 TRANSFAC yes 114107746
chr11 78798362 78798370 FEV JASPAR yes 40066299
chr11 78798362 78798370 FEV JASPAR yes 114107747
chr11 78798362 78798458 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 107992999

Genes associated with rs566990143[chr11:78798362], comfirmed by eQTL
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Blank TSI value indicates lack of sufficient expression for calculation
Chrom. Start End Strand Gene name Ensembl ID TSS of gene Distance between TSS and SNP Tissue q Value id More