Tag | Content |
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EnhancerAtlas ID | HS118-09495 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr2:8388320-8389870 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nfe2l2 | MA0150.2 | chr2:8388895-8388910 | CAGAATTACTCAGCA | + | 6.03 | RAX | MA0718.1 | chr2:8389657-8389667 | GCCAATTAAC | + | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 8388692 | 8389197 | chr2 | 8388400 | 8388800 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I008248 | chr2 | 8388692 | 8389197 |
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Enhancer Sequence | TCCCAACACG AGGCCCTCCT TCCCTGTAGC CTCACCCTGT CCTCAAACAC TGTGCATTTG 60 GCAACATGTG AGTTGGGTCT TCATCCTCAA AACCCACCCT CGAAACACAA CATGCATGTC 120 TATACCTCCA CCCTGGGGTC AACACTTGGC CAGCCAGGAG AGGCCTTGAC CACACTCCTG 180 GACCCTGTCA TCTTTCCTTC CTCCATAGGA CAGCACAGAA ACTCAATAAA TGCCTGTGGA 240 ATAAAGCACA CATTTTATTT TTGAATCCAG TCTCTGTTCC CCACAGAGCA CGTAAGCGTG 300 AAGGCAGGTC TGTCTGCTTC CTTCACGCCC ATATCCCAGC ACTTACTCAG AGCCTATCAA 360 CCAGCCGGAG CTCGAGAAAT AGATGATGAC AAAGTAAATA AATTCATCTA TGGAGATACT 420 AAAGCTTTCC TAGGACTGGC AAAAAGGAAA ATCTTCAACA CAGCTAATAC CCGATTTGCA 480 GATCAACTTC GTGTTATTGT CACTCATAAA TGCCCTAGCT GATTTGCATA GCAAAAATAA 540 GATTTCACTG AATGCCACAC TCAAATCACT TTGCTCAGAA TTACTCAGCA GAGGGCTGGA 600 TTTGTAAATG TGTTTAGTTT GGAAGTTCCT GACTTCACAA AAGTTACTTT CAGTTACTAG 660 GAATTTTCCA GTACATTTTC TTTGGCTTTA TAAAAAAAGA TCTGATCCAA TCATGATTTT 720 TCTCTCTAGA ATTTCTACAT TTAGCTTCAG GATTTATCAA TGACATTTTT TCAAAGCAAA 780 AAAAATCTCT TCAGCCAACA GTATATCTGT TTCAGAAGGG AAAGTTGGAT TTTTATTTCC 840 CCCTTTTTGA AGCCGTTGGT GCATCTGGGA GAGCTCGCAG TCTTACCAAA AGCTTCTCTG 900 TGGTGGCTTT GGGGAGAACA GCAAATTTGG AATCTCACTT GCCAGTGGTA TAGGCATCAG 960 AGTTCTTAGT GGACTTTTGC CAAAGGCCAT TAATAAAATA CAGTCCAAAT GTCCTAATTA 1020 GCATGCCCTC GAGTGTGGCC ACGTGTAGAA CTTGGACTGG CTCTTGGCCA CGAGCTGCTG 1080 TCGCAAAGCT CAGATCCCTG CTTCAAGCAG GCTATGTCAC AGAGAATCCA CTGCAGAGAG 1140 CCTTCTGGAG ATCGGGGCAA TGTGCGGAAG GGCACGTCCC TGCCAGCCAC CCGTACTCTG 1200 GCCAGGACCC GGAGCTGGGC ACTGGCCGCA CCCGGCTGAG AGGTGATGTC AGATGTTCCT 1260 GTCGGGATCT GGCTTCTGGC TAGCAGCAAC TCCCGTGTAA TGGAAGAGTG GCTTCCCTGC 1320 TAAGCTTCAA CCCTGAAGCC AATTAACGAC TCAAATCCTT CAGGAAGCAC TGCTTGGGTT 1380 TTACCAGAGA CATAAAGGTC TTATCCCATT AATTGGTGCT TAAATAAAAA GAATAAATAC 1440 TGCAGAATCT AACCTAGAGT TGGTCCCTAC CTTTCGCTAC CCTGAATGTA CTATGACCCT 1500 AGAAAACACT TATTTTATAA GTAGTTTTTT AAAATAAAAA TAAATACCCT 1550
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