| Tag | Content |
|---|
EnhancerAtlas ID | HS091-21216 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chr17:74294920-74296000 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr17:74295400-74295419 | TGGCGCCACCAAGTGGCCA | - | 6.82 | | RARA | MA0729.1 | chr17:74295601-74295619 | GAGGTCAGAAGTTCGAGC | + | 6.44 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TCCCGACCTC AAGTGATCCG TCTGCCTCGG CTTCCCAAAG TGCTGGAATT ATAGGTGTGA 60
GCCACAGCGC CCGGCCCTGA GTGTAGTTTT TATTTGCTTT TGTAGCTTTT CAAACTTTCT 120
TTACAGTCTG TCCTGAAATG CAGGGATCTT TCCTTATTAG TGGGCCATGG TGACAGACCC 180
TGGAAATAAA ACTTCTGTAG GGGGCCCTCT GCTGATGGCA ACTTTTGCAC ACAGGCATGC 240
ATCTGTCTGT CTTGAGACAG TGTACAGATG ACCAAATTGT TTTCCGATCG CCAACCTACC 300
TTCACCTGAA TAAAATCAAG CTGAATATGT TCAAATGGCC CTCAAAGATG AGGCTTAACT 360
TCCCTTTTGG TCTTGACATC CCTCCCGCTG GCTTTGGGCT AGTGGGTTAT CAAAACAAGC 420
AAGCCAACTT TGAGGGCCAT TTGAAAATGT AGACGGAAGC AGGGTGAAGA GTAAAGCTTT 480
TGGCGCCACC AAGTGGCCAT CTTGGGGAGC GCCAAATATC TGGGTACAAA AGACAACCTG 540
GGATCTCCAG GACCATTTTC TGATTTCAGG GCTCATTCTC AGAGGAAAGC GGCATCAGAA 600
AGATGTTGCA AGAGGGGCCG GGCGCGGTGG CTCCAGCCTG TAATCCTAGC ACTTTGGGAA 660
GCCGAGGCGG GCGGATCACC TGAGGTCAGA AGTTCGAGCC CAGCCTGGAC AACATGGTGA 720
AACCCTGTCC CTAGTAAAAA TACAAAAATT AGCTGGGCGT GATGGTGGGC GCCTGTAATC 780
TCAGCTACTC GGGAGACTGA GGCAGGAGAA TCATTTGAAC CCAGGAGGTG AACGTTGCAG 840
TGAGCCAAGA TTGCGCCACT GCACTCCAGC ATGGGCGACA AAGCAAGACT GTCTCAAAAA 900
ACAAAACTAA ACGATATTGC AAGAGGACCC TGAACACAAA AGGAATGGAC TAGAAAAAAG 960
TGGCCTCCAC TTTCACTTTT TTAAAGCCAA ACCTTTTTTT TTTTTGAGAC GGAGTTTCGC 1020
TCTTGTTGCC CAGGCTGGAG TGCAGTGATG CGATCTCGGC TCACTGCAAC CTCCGCCTTC 1080
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