Tag | Content |
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EnhancerAtlas ID | HS091-34761 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr3:100353280-100354520 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr3:100354185-100354206 | AATTGCTTTCAGTTTCTGTGC | + | 6.48 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_28516 | chr3:100353280-100356394 | Fetal_Intestine | SE_29227 | chr3:100353063-100356546 | Fetal_Intestine_Large |
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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 |
GH03I100634 | chr3 | 100353439 | 100356248 |
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Enhancer Sequence | TAACACCATA AATAGGTATT AATGTACACA TTTTATAGAT GAGGAAAATG TGGTTCTGAG 60 AGGTGAAGCA TTTTGCCTAG TGATCACAGC TAAAAAGTGA TAGAGCTGTT CTTTATTTTA 120 AAGTTCACAT TGTACTACCC TGGCTCCCTA ATCACAGATG GGCAGGGTAG GGGTTGGGTG 180 GGAACAGAAG TTGGAGAGTG GATGTGGCTG CCAACCACAC AAGTTGTGCC AACCCACAGA 240 TTGAGGAAAG ATGCTAAATT TGGAATCTGG CAAACCAGTG TTTGGTTCTT AGCTCTGCCA 300 CTTCTAAGCT GTGTGAAACT TGGTTGAGGT CCCTAACTTC TCCTGAGGGT GAACAACTCA 360 CAAAGTTGTT TTGCTTATTA AATGTGATAA CACCTGTAAA CATCTAACAG AGTGCCTAGC 420 ACATAGCAGG GATCTAGCAA TTGAATTAGG GTTATTTGTT TCTGTCTACT GATTGGGTAT 480 TGTTTCTGAC ACTTACCCAA GTGTGAATAG CCTATAACAC TGGTATAATT TGTGAAATGA 540 TGCTGCCATC TAGTGAAAAC CAAGACACAC ACACACACAC ACACACACAC ACATACACAC 600 ACACGTGCGC GCGCATGGAC ACCCAGCTTC ACCAATGACA ATATGGATTG GCATGTTTTA 660 GCCTCACAAC ACAGAGCCCT GGGGCTAACT GGCACCTAGA GAGGTCATCT CGGCCAGTGC 720 CTTCCAAACT ACCAGTGCTG AAAAGCCAGT TCAAAAAATT TTGAACCCAT TGCACACCAA 780 TATTTTTGTG AAATAATAAA AATAAATTAC TGGAAAAATG AAATAAAAAA TATGTATAAA 840 ATACAAACCA AAATTTTAGA ACTGTTAGAT TCAACAGCAA AAAATTGCTA TATACATCTC 900 TGACCAATTG CTTTCAGTTT CTGTGCTTAT CTCTCTACGA CCTTTGTAAC ACACAGTGAA 960 CCAGCGCTGG CCCATGGATA CACTCTAGTA GCCCCAATCT AGCTAAGGCA GCCCCTTATA 1020 GTTAATCAAT CCTGTCAAAC AGGAAAGGCT GGCAAAACCA CTGGTCTGCA TGTACTTTGT 1080 CCTTTACACA AGGAAGGATG CAAACGTGGA AAACTGAGTG GACATGGTGT TCAGGAGATT 1140 GAGGCTCAGC TAAATTCCAG CTTATTTACC TGCAGTTGCT TACAAAGTGT TTGGACATAA 1200 TTGTGTAAAG CTAGGGTTTT TTTTCTGGTT TTTAAAACAG 1240
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