| Tag | Content |
|---|
EnhancerAtlas ID | HS091-00607 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chr1:17731710-17733250 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:17732831-17732850 | TGGTGCCCTCTGGTGGGCA | - | 7.57 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH01I017406 | chr1 | 17732761 | 17732930 |
| Enhancer Sequence | ACACAGGAAT AAAAAACAAA CAGCCTTCCC TTCAAGACTG CCTGTGTGGC CGGGCGTGGT 60
GGCTCACGCC TGTAATCCTA GCACTTTGGG AGGCTGAAGC GGGCAGATCA CTTGAGGTCA 120
GTTTGAGACC AGCCTGGCCA ACATGGTGAA ACCCCGTCTC TACTAAAAAT ACAAAAATTA 180
GCAGGGCGTG GTGGCACTTG CCTGTAATCC CAGCTACTCA GGAGGCCGAG GCAGAATTGC 240
TTGAACCCAG GAGGCAGAGG TTGCAGTAAG CAGAGATCAC ACCACTGCAC TCCAGCCTGG 300
GCGACAGAGC AAAGCTCCAT CTCAAAAATA CAAGACCGAG CGCGGTGGCT CATGCCTGTA 360
ATCCCAGCAC TTTGGGAGGC GGCCAAGGTG GGAGGATCAC GAGGTCAGGA GTTCGGGACC 420
AGCCTGGACA ACATGGTGAA ACCCCATCTC TACTAAAAAT ACAAAAATTA GCCAGGCATG 480
TGGTGGACAC CTGTAATCCC AGCTACTCAG GAGGCTGAGG CAGGAGAATC GCTTGAACCC 540
AGGAGGCAGA GGTTGCAGTG AGCTGCGATT ATGCCACTGC ACTCCAGCCT GGGTGAAAGA 600
AACTCAGTCT CCAAAAAGAC TGTCGGAGTG GACTGCAGGA GTCAGGGGCG AGACACACGA 660
CACTCAATTT GCAGCATGTG CCCAATACAC AACAGCCAGT GTGTCAGCAG GGACGCTGCC 720
CCCAGCAGTG GCTTCCCTGC CCACGGGGGC TCTTCCAGGG CAGGAGCATC TGATGGGAAG 780
CTCCAAGCTG CCAAGGGGGG AGATGGGGAA ACACCGTGTT TTACATTTGG ACTGTCCTGC 840
AACAGTGCAC ATGCTCCTTC TGCAGCTAAC AGGCCATGGG AGACCGTTTC CTCCTCTCCC 900
AAACTGGGCC AATGCCTGCC AGGAGGGGCT GGTCTGGACA CTATTCAGCC AGTCAACACA 960
AGGTGGCCTG CACTCGAGGT TCCAGGGATC CCAGGCATCT TTGCGGCTGC AGGGAGCCGG 1020
TGTCCTGTGC AAGGGTCTGG TCTAGGACTC TGCCCGGTAT AGACTCAGCA GCAGCCTAGA 1080
AGGGAGAGTG TCCGTGATCT CTGAACCTAC GACCAGCCTC CTGGTGCCCT CTGGTGGGCA 1140
GTTGGCCACA ATGCCTGCAC AGAGCAGCAC TGGCCTGAAG CCACAGCCGG GGCCTGACCA 1200
GAGCCCCCTG CTGAAGTCTG GGGAGTGGGT GCACATGCAG TCACCGCGCT GGATGCCTCC 1260
CATGACTTAT TTTTTTCCTC TCAAAGCCCC AGTGAAAATG CAAAGAACTC CACTTCTGAA 1320
TTGGACAACT GAGGTACTGA CTCTGTCCCA CTCCCCTAGC ATTTCATGGG GCAGAGTTGG 1380
GGGATCCACT CACTTCAACC AGTGCAGTTT AAACCTGGAA GCTCCCCTGG GGCCACATGT 1440
CTCCTGGCAC CACCTTCTGT GGGTGCCAGG GCTTAGGAGG TACACATATA AGGAGTTAAG 1500
AAAAACAGAG CTCCGTTCCA ACCGAAAAAG AAATGCAAAA 1540
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