Tag | Content |
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EnhancerAtlas ID | HS050-48849 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr3:136499080-136500170 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MSC | MA0665.1 | chr3:136499800-136499810 | AACAGCTGTT | + | 6.02 | MSC | MA0665.1 | chr3:136499800-136499810 | AACAGCTGTT | - | 6.02 | MYF6 | MA0667.1 | chr3:136499800-136499810 | AACAGCTGTT | + | 6.02 | MYF6 | MA0667.1 | chr3:136499800-136499810 | AACAGCTGTT | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GACTGCAGCT ATGGGTCACG AGCAATGGCA GGACAACTCA GCAGTCAAGA ACCCAGCTAC 60 AGTGGAACAG TAAGTCTATG CTGGGGTGGG AATAGGGTAG GTGGGCACCT CTGCTTTGCC 120 CCTTGACAGG AACTGACAGG TGAGAGAGTT GCCAGATTTA CTGATACGTG TTGATGGGCT 180 CATTGTCTGT GGGAAGCCTC CTGTACTGTG GAGAATGACA TGGACAAAGC CAGAGGAGGA 240 AGAACAGTCC TCAGCCCAGA AGACGGATGG TTGCTTCTCT GGCCTAGGTG TTAAGGATGC 300 TTAGAGAGGA GACAGCTCCA TCTTCATTGG ATTTCCAGTC TACACCAGAT GCCAAACCAA 360 TATGAAGTAG AAACAGGGGG AATTTTTGCC ACAATTATCT GCCATAATGA TTTCTCTTCT 420 TACTACCCTG TCTTTTTACA CTTTAACTAT GTGTTGCATT AAATAGTTGA GTTTTGCAGT 480 GAAAAAAGGT TGCTAAGCAG GATTTACACA ATAAATTTAA AGATAGAAAC TAGAAAAGAT 540 TTCCATTCAC ATTTCTAGAA GCAATTAATT AGAGAGATGT AAGGAAGACA GAGTGGACAG 600 AATGTTTGCT GTTACTCAAC TGTCAACAGG CAATTAGAAT AAAACTGGTG TGTGAAAAAC 660 ATGACCCCAT CATGAGATGG AGGACATGGC TGCAAGGCCA GCAGCCAATG TAATTGGTGA 720 AACAGCTGTT GCAAGTACAA CTTTACAATG TTACTTTAAC ATAACACACA TTGTCTTTCT 780 AAACAAAATT CATAGTTATT CCATAACAAA TGAATCGTGG CCAGGCAGGA GCAGTGGCTC 840 ACGCCTGTAA TCCCAGTACT TTGGGAGGCC GAGGCGGTGG ATCAAAAGGT CAGGTGATCA 900 AGACCAGCCT GGCAAACATA GTGAAACCCC GTCTCTACTA AAAATATAAA AAATTAGCCA 960 GGCGTGGTGG TGGGCACCTG TAATCCCAGC TACTCGGGAG GCTGAGGCAG GAGAATCACT 1020 TGAACCTGGG AGGCAAAGGT TACAGTGAGC TGAGATCGTG CCACTGCACT CCAGCCCTGG 1080 CTACAATGCG 1090
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