Enhancers that regulate NFRKB[ENSG00000170322.10]
Back to top
Chrom. Start End Enhancer ID TSS of gene Distance between enhancer and TSS Tissues that enhancer appears More
chr11 129666205 129676135 enh62225 129765485 89350
chr11 129687139 129712395 enh58393 129765485 53090
chr11 129695386 129695610 vista12146 129765485 69875
chr11 129714270 129719175 enh29267 129765485 46310
chr11 129716429 129716681 vista12147 129765485 48804
chr11 129717042 129717234 vista12148 129765485 48251
chr11 129720125 129724275 enh80053 129765485 41210
chr11 129723853 129724184 vista12149 129765485 41301
chr11 129730176 129730501 vista12150 129765485 34984
chr11 129731747 129732130 vista12151 129765485 33355
chr11 129781322 129781453 vista12152 129765485 15837
chr11 129800254 129800364 vista12153 129765485 34769
chr11 129805498 129811893 enh60337 129765485 40013
chr11 129818145 129822955 enh14397 129765485 52660
chr11 129828273 129846484 enh2109 129765485 62788
chr11 129857425 129868975 enh2110 129765485 91940

Transcript facotrs that regulate NFRKB[ENSG00000170322.10]
Back to top
Chrom. Start End TF name Source Predicted site? Tissue TSS of gene Distance between TFBS and gene id More

Chrom. Position dbSNP ID Reference Allele Alternative Allele Distance between TSS and SNP Tissue q Value id More
chr11 129723865 rs7117897 C T 9666 Esophagus 8.41711e-21 2366871
chr11 129765280 rs143303873 C CG 0 Heart 3.50718e-09 2366988
chr11 129765453 rs3108962 A G 0 Spleen 0.000104472 2366990
chr11 129720249 rs113656064 A G 13282 Uterus 0.266239 2366804
chr11 129723865 rs7117897 C T 9666 Thyroid 3.35569e-14 2366871
chr11 129765280 rs143303873 C CG 0 Liver 8.5598e-12 2366988

Genomic Location chr11:129733531-129765485[-]
TSS 129765485
Gene Name NFRKB
Ensembl ID ENSG00000170322.10
ENTREZID 4798
Uniprot
Q6P4R8
A0A024R3K9
Protein Name
isoform CRA_a
isoform CRA_c
Nuclear factor related to kappa-B-binding protein
Nuclear factor related to kappaB binding protein
Nuclear factor related to kappaB binding protein
Nuclear factor-related to kappa-B-binding protein