Tag | Content |
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EnhancerAtlas ID | HS180-03905 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:185408550-185409640 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr1:185409413-185409434 | AAAAAAAAAGTGAAAACAATC | - | 6.36 | JUN(var.2) | MA0489.1 | chr1:185409019-185409033 | ATGAGTCATTTTCA | - | 6.3 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I185438 | chr1 | 185408004 | 185412576 |
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Enhancer Sequence | GGCTCTAGGT TCATGGGTTA TTAAGAAAAA AGCAACCCTT GCTTGTGGTT ATAGGAAGGA 60 AAAGGTTTCA GTTATGAAAA GAAGATGAAC ACCAACTGGG AGTCCCCAGT AGCCCAGTAA 120 AGGAGAGGAT AGAGAAGGTG GGGGGAATGA ATGGAGGAGT ATGGGATCCA GACCGGAGGG 180 AGATGGGTGG ATGAATGATA GGGTCTTAGG CTTCTGAGAG TGGTTGAGTT AAAAGGGAAT 240 AAAGCATGAG AAATTCATTT TGATGGCCTC TTCATGGAAG GCCCAGAAGT TCAGGTCTCT 300 GTCCCATACT ATAACTAGAA GGAGTGGAGA AGCTACAGAT GAAAGGTGTT ATATGAGCTT 360 CCTTGGGGTT TCTGGCCTCA GCTAGAGGTC CACCAGCTAG AGGTTCTTAT TGTGACTGAC 420 TAGCTGCATG CCCTTGGGCC AATTCTTGTC TGCTTTCCTC ATGTATAAAA TGAGTCATTT 480 TCAGTGCTCA TGTGCTATTC TCATTCTCGG GAATGGTTCT TACTTCCTTG TCAGCCTGTT 540 GAAATCCTAG ACATTCTAAG AATTATCTCA GAAGCTGTCA TTAGGCTATT CTCAATGTAA 600 TCACCCAATC AACCAGAAGT GACATTTCAC TTCTCAGAAT CACTGTTACA CTGTCTGAAC 660 CACCCTCATG ACAGTTATCA ACATCTTCTA ACTAATAGAG TTATTTGTGT TTATCTCTCA 720 TATATGTTGA AAACACCATG AGAATAGGAG AGGTGACACA TTCTTTTTGC TCATAGCAGG 780 TGCTTGATAA GTGTCTGTCA AATGAACCAG TAAAGCATAC TTCTGGAGGA CAAAGTAGTC 840 ATGAAGTAAT GGAGACTTAT TAGAAAAAAA AAGTGAAAAC AATCTTGTAT TTCAAATTTG 900 CATGAGACAT TTAGGTCAGT GGAAAATGTG ATGTCATCAG GTCTAAGAGT TGCTTGTGTG 960 GCTGTTGCCA CAAACTTGTG TCAGTTACAG ATAGAATAAA TCTATTAGCA GAGAATTAAT 1020 TGCTGTATGC AGATAGCTTC ATGGAGTTGA AATAATTCTG CCATGTTAAG TGGAAAATAG 1080 CAGAGGAAGA 1090
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