Tag | Content |
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EnhancerAtlas ID | HS076-05864 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr1:231527870-231529270 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFYA | MA0060.3 | chr1:231528755-231528766 | AGCCAATCAGA | + | 6.32 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_40940 | chr1:231528222-231530264 | Left_Ventricle |
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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: 2 | ID | Chromosome | Start | End |
GH01I231392 | chr1 | 231528547 | 231528746 | GH01I231393 | chr1 | 231528957 | 231532952 |
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Enhancer Sequence | AAAATACAAA AAATTAGCCG GATGTGGTGG TGGGCGCCTG TAGTCCCAGC TACTTGGGAG 60 GCTGAGGCAG GAGAATGGCG TGAACCTGGG AGGTGGAGCT TGCAGTTAGC CGAGATCGCG 120 CCACTGCACT CCAGCCTGGG CGACAGAGCG AGACTCTGTC TCAAAAAATA AAATAAAATA 180 AAATAAAAAT AAATAAAGCA CAAAACATTT TAAGAGAAAA ACTAAGAACT TAATTTTAAA 240 AATTTTCCAC TATAATACTT AAAGTAAATG CTATTTAAGT CATATTAACA ATTATTTATT 300 AAGCATACTA TGTAGAAAAA TTGGTGGCCC AGGTCTGTCT GATTCACTAT ATGCTGTCAA 360 CCAGTGTAAC TAGACAAAAT GTGAAAACTA CAATGAGAAA ATTACAAGTA AAATGTTATG 420 GTGGTAATAG AGAGGGTGAG GTATGGAGCT GTCCAGCCTG AATTCAAATC TCAGCTCTAC 480 CACTTCCTAG CTGTATTTGG AAATAATGAC AGTATACACT TCAAAAACCT ATGGTGAGGA 540 TAAACAATAG AATACATGTA AAAGACTAGC ATAGCACCTG GTACCTAGTA AGCATCTAAC 600 AAATGTCACT TATTTTCATC ATTACTGACA GTCTCATAAT CTTTATCTTC ATCCTCAAGC 660 AGTCACAGGT GAGATTTTTC ATCCCTGTCC ACGTGTGGAC AAGCAGCTTT TGTTTGCCTG 720 GCATCCATTC CCCTTCTTCT CTTTCCAGGT GCCTCATTTA CTTGGGAAAG CCTGACCTGT 780 AGTCCTCAGT TCTCACCCCT AGGTGAGGTT CACTCTCTAC CCTCCAGGGT GGACATGTGG 840 CTCAAGCCTG GCCAGAAGTT GGTTCAGAAA TGGGCAAAGG GCCTAAGCCA ATCAGAGGCA 900 ACTCCAGGAT TTTTGTCAAA GCCCTTGGTA AAGAGCAGCT CTCTTTCTGT ATGTATCTCC 960 ATGATGTAAT GCTGAAACTA TTAGGGCCAT CTTGTTGTCA TATCAGGGAG CTTACAAGAG 1020 AATAACTAAT ATAGAAAAGA AAAGCTGAGA GATCAAGTTT TGATAATATT GTTTGAGCCC 1080 TTGGTTCCAA CTCTGCCAGT CAATCAGCAG ACCCATAGGT AAGGACCAAT ACATTTTGTT 1140 CTGGTTTGCT TAAGCTCATT TGAAAGATTT TTGTTTTGTT TCGGTTATTT GCATCTGAGA 1200 AGCTCTATAA CACGTCAGGT ATCAATCAAG AGCCAGAAGC TGGTGACCTA AAATATAGTA 1260 GAGCTTAGAA GGGCATGGAT TTGGAATCGG AGAGATCTAG TTCCTAATCT TGTTTCTAAC 1320 AATTACTAGC TGCGTGGCCC TGGGCATGTG TCTAATCCTA CTTCTTCATC TGTAAAATGG 1380 CTTAATACCT GCCTCAAAGG 1400
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