Tag | Content |
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EnhancerAtlas ID | HS076-00539 | Organism | Homo sapiens | Tissue/cell | H1 | Coordinate | chr1:11649730-11651120 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
INSM1 | MA0155.1 | chr1:11650247-11650259 | CACCCCCTGACA | - | 6.22 | Nr2f6(var.2) | MA0728.1 | chr1:11651076-11651091 | GAGGTCAGGAGTTCA | + | 6.22 | ZNF263 | MA0528.1 | chr1:11650595-11650616 | CTCACCCCTCCCCTCTCCTTC | - | 6.19 | ZNF263 | MA0528.1 | chr1:11650598-11650619 | ACCCCTCCCCTCTCCTTCTCC | - | 6.27 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ATGTGGCTGG GAGTTAATGG AGTATGGGAA GGGTCAACTT CCAAGCTAAG GAGGACTGGT 60 GGACATCTCG TATCTACAGC CCTTCAGGGT CCCTGGCAGC ACCCACATCC CCCAGGCTGG 120 AGGTGGGTCA GCTTCCTGAT AGATCCAGGA GGCTAATTTC TCACTAGGAA GTCAATCCAG 180 ACTTCATTTC TCATTTTGCC ACAGGCGGCG GCCAGATGGA CGCATTGGGC ATTGGTCACT 240 GTGCCGTTGG CGGCTGGGGC ATCTCCAGGA CGTCTACACT GGGGTTCGGG TGAGTGGGTG 300 TTTACACCCA ATCTGTCTTC ACCTTGAAAC TTACACTTGG AAGACGAGTA TGACCTTTCT 360 GAGGCCCTCC TGATCCTCCG TAGTCAACCT TCTGTGACTT CCTCCAGTGA CAGATGCTCT 420 TGGTCCTGCA CCATGTCCCT CAGCACTCAC CTCCACACAC CAAAGCTGCT GGCTGCAAAT 480 ACCTCCAATT CACTCCCCAT GTTCCAGGAA GCAAGGGCAC CCCCTGACAT GGTGGCCACT 540 CCAGCCTCAC CCCGGGCACA GCTTCCGCAA GGACTCTTTG GTGGATTGAT GAAGGTGGGG 600 TAAAACTTGA ACTCTAGATC TTCCATGTAG ACCACCCCAA ACTTATCAGC AGCAAGATTT 660 ACTCAATCTC ATGAATATGA CCCCTAAAGC TCAGAAACCA GGGCCAATGA GGAGGCCACC 720 TCCCTGTTGG TTCACTCATT GAAGGCATAT TTACACAGCA CCTAATATGT GCCAGGCAAT 780 GTGATGGATA CTAGGAATAC AGCAGTGAAC AAAACAGCCT CACGCCCTGA TCTCCCAGAG 840 GCAAGGCCTT AGAAGGTGAG TGTGGCTCAC CCCTCCCCTC TCCTTCTCCT GGGCATGCCG 900 GAAAACTACA TTTCCCAGCT CCCCTTGCAG CCAGGGTGGG GCCATCTACC TGGATTCTAG 960 CCAATGAGGT GCAGGTGGAA GTGGGCACCA CTTCTGGGTC TGACCATAAA ACCCCTATAA 1020 TTTCATCTAT ACTTTCTCTT CCTCTCTTAC ACTGACTTCA AGGGCACAAA TTTCAGATGG 1080 GCAGCATCAC ACAGCAGGAT AAGCCTGGAT CCTGTACGTC CTGCCTGGAA GAGGGCAGCC 1140 AACTGGCATT GACCAATCTA CATGAGACTG CAGCTAGAGT AAGAAACACA GCTCCCTCAT 1200 GTTAAGCCAC TGCTGACTAA TGAAATAGGC TGGTGACTGA GTGTGGGAAA GTGTATTTTC 1260 CAAAGATGGT CAACAATACT GGCCAGGTGC GGTAACTCAC ATCTGTAATC CCAGCACTTT 1320 GGGAGGCCAC AGTGGGCAGA TCTCTTGAGG TCAGGAGTTC AAGACCAGCC TGGCCAACAT 1380 GGTGAAACCC 1390
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