Enhancers that regulate INSC[ENSG00000188487.7]
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Chrom. Start End Enhancer ID TSS of gene Distance between enhancer and TSS Tissues that enhancer appears More
chr11 15031605 15035755 enh111732 15133970 98215
chr11 15046665 15050815 enh96178 15133970 83155
chr11 15072885 15079395 enh101245 15133970 54575
chr11 15110905 15117275 enh1649 15133970 16695
chr11 15143379 15147772 enh43499 15133970 9409
chr11 15161065 15170315 enh1650 15133970 27095
chr11 15176812 15181010 enh94867 15133970 42842
chr11 15179085 15179582 vista9744 15133970 45115
chr11 15214645 15219255 enh87851 15133970 80675
chr11 15219194 15219222 vista9745 15133970 85224
chr11 15228245 15232395 enh111733 15133970 94275
chr11 15233485 15237635 enh50721 15133970 99515

Transcript facotrs that regulate INSC[ENSG00000188487.7]
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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
chr11 14277913 rs143720263 C CTAA 856057 Esophagus 0.299644 1868496
chr11 15840652 rs1920673 G A 571898 Esophagus 0.267669 1874603
chr11 15128353 rs138352484 C A,T 5617 Ovary 0.417996 1871602
chr11 15654141 rs117059452 A G 385387 Uterus 0.472434 1873427
chr11 15050361 rs73422642 A G 83609 Thyroid 0.132433 1871383
chr11 14275550 rs10832239 A T 858420 Liver 0.0960888 1868479
chr11 15050149 rs143903693 A G 83821 Stomach 0.189855 1871381

Genomic Location chr11:15133970-15268754[+]
TSS 15133970
Gene Name INSC
Ensembl ID ENSG00000188487.7
ENTREZID 387755
Uniprot
Q1MX18
Protein Name
Protein inscuteable homolog