Tag | Content |
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EnhancerAtlas ID | HS098-14017 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr12:93531220-93532310 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOS | MA0476.1 | chr12:93531997-93532008 | AATGAGTCACA | - | 6.62 | RUNX1 | MA0002.2 | chr12:93531822-93531833 | AAACCACAGAG | - | 6.14 |
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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 |
GH12I093137 | chr12 | 93531204 | 93533775 |
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Enhancer Sequence | GGATAGACGA GAGAGATGCA AGTTTGCAGC AGGAGATCAG CTCTCCAAAC TTCACATCTT 60 ATAAATTCCT TGATTCAACA AACATTGAAA AGCTTAATGC TGTCATTATG CCTCTTGCTC 120 TATCCTTGGG AAACAGAACC TGGCACACAG ACATGCCCAA TCAATATTTA TTGAATAAAG 180 GAATTAAGGA AAGAAAAAAG ACAATATTGT AATGGCATCA TTATTAAATG GTTTTCTGAA 240 TAGGCTGCCT CTGCTATGAG ACAAATAGCT GAGATTCTCA CAGATTTCCA GTTTCCATAC 300 TAGCAGGCAT TGAGATCCAG GCAAAAGGAG GTTAATAGTG AAACACAAGC CAGAGAGAAA 360 TTCCTCCCCT TCATCTCTGG TGCCAACATC ATCAAATACC AGTCACTGGC CAAACCTGTG 420 TTTATTCCAT GCCCTGTGGC CTAATGAGAG GGGATGGGAC AAGAAGCAGC TCTGCTAATA 480 ACTGTCATGA AAATAATAAT ATCACTTGGC TGTATGCGGC AACTTTCATT GGAAGCTCTT 540 GAATCAATTT TTTCCTCTTG CATAACTATT ATTTCCATTT TATTTCCACT AAAGGAGAAG 600 CCAAACCACA GAGTGGTTGT GACTTGCCCA AGGTCATGGA GCAAATCAGA AGAGCAGTTT 660 TTAAAAGCTG AGAAGGATAT CAGGGGATGT AAAATCCAGT TGCCTTCCCA GCCTAGAATG 720 GGCTGGGTTC ATGACTCAGT AAGACACATG GCGTTACCTA AGCTCAGTGT CTCTGAAAAT 780 GAGTCACACT AAGGGAGACT CAGGGCCTGA GGGGCTGTGT CAGACATACG TTTTCAGTAG 840 TCACTCATTG TCCCTGCCCA TCAGATTTTA ACGTCTGTCA CCGAAGCCCA TCACAGACAG 900 GGCCTCTTGG GAGGTTTAGC CTATGGAACT GGGAAGGTCT GCCTTGGGGG TGTCTGTCTT 960 TTCTGGATGT TTACCCAGCT GTCAGTTCCT ATGAAGCCCA GGTCTCCCCA TTCCATTATC 1020 CATCAGGAGC CCATGGCTGG GGTAGCTGTG GCTTCCACTC GGTCCATGAT GATTCTGGTG 1080 TTTGCCTGTT 1090
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