Enhancers that regulate FAM169B[ENSG00000185087.7]
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Chrom. Start End Enhancer ID TSS of gene Distance between enhancer and TSS Tissues that enhancer appears More
chr15 98957223 98957617 vista21364 99057611 99994
chr15 98964843 98965105 vista21365 99057611 92506
chr15 98969685 98973835 enh47906 99057611 83776
chr15 98974419 98978965 enh44215 99057611 78646
chr15 98997205 99001355 enh96648 99057611 56256
chr15 99045265 99049535 enh16454 99057611 8076
chr15 99090927 99091248 vista21366 99057611 33316
chr15 99091450 99092159 vista21367 99057611 33839
chr15 99093365 99102215 enh69012 99057611 35754
chr15 99103380 99113555 enh58686 99057611 45769
chr15 99111126 99111513 vista21368 99057611 53515
chr15 99121943 99126155 enh44216 99057611 64332
chr15 99123840 99124144 vista21369 99057611 66229
chr15 99141565 99145815 enh99301 99057611 83954
chr15 99146405 99150555 enh88209 99057611 88794
chr15 99150739 99155239 enh89783 99057611 93128
chr15 99155861 99160301 enh89784 99057611 98250

Transcript facotrs that regulate FAM169B[ENSG00000185087.7]
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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
chr15 99603464 rs185685390 T G 545853 Esophagus 0.11363 4223378
chr15 99414412 rs117834065 C T 356801 Breast 0.284414 4222027
chr15 98551795 rs9330522 T C 428596 Spleen 0.0624491 4215672
chr15 99558634 rs73468258 C G 501023 Uterus 0.469422 4223043
chr15 99364750 rs148876620 AG A 307139 Stomach 0.253776 4221543

Genomic Location chr15:98980391-99057611[-]
TSS 99057611
Gene Name FAM169B
Ensembl ID ENSG00000185087.7
ENTREZID 283777
Uniprot
Q8N8A8
A0A0A0MR76
Protein Name
Protein FAM169B