| Tag | Content |
|---|
EnhancerAtlas ID | HS081-21325 | Organism | Homo sapiens | Tissue/cell | HACAT | Coordinate | chr9:134245470-134246600 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HES2 | MA0616.2 | chr9:134245546-134245556 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr9:134245546-134245556 | GGCACGTGCC | - | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr9:134245799-134245814 | GAGGTCAGGAGTTCA | + | 6.22 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTTGGCTCAC TGCAACCTCC ACTTCCCAGG TTCAATAGAT TCTCCTGCCT CAGCCTCCCA 60
AGTCACAGGG ATTACAGGCA CGTGCCACCA CGCCCAGCTA ATTTTTTGTA TTTTTAGTAG 120
AGACGGGGTT TTACCGTGTT AGCCAGGATG GTCTCGATCT CCTGACCTTG TGATCCGCCC 180
ACCTCAGCTT CCCAAAGTGC TGGGATTACA GGTGTGAGCC ACTGCACCTG GCCAGTTTCC 240
TCATTTCTTA AGTGGGGCAA TAAGGCCGGG CACAGTGGCT CATGCCTGTA ATCCTAACAC 300
TTTGGGAGGC CGAGGCAGAT GGATCACTTG AGGTCAGGAG TTCAAGACCA GCCTTGCCAA 360
CATGGTGAAA CCTTGCCTCT ACTAAAAATG CAAAAATTAG CCAGGCATGG TGGCAGACGC 420
CTGTAATCCC TGCTATTCAG GAGGCTGAGG CAAGAGAATC ACTGGAACCT GGGCGGCGGA 480
GGTTGCAGTG AGCCGAGATC GCACCACTGC ACTCCAGCCT GGGCAACAGT GAGACCCTGT 540
CTCAAAAAAA TAAATAAATA AATAAAAATA AAATAAAGTG GGGTAATAAT AGTACCTGCT 600
GCAGAGGGTT GTCGTAAGGA TTTAATGAAT TGATGCATGT AAAGCACCTG CACAGGGCTA 660
GGACGTGAAG TCAGAGTGCA CTGGCTGTTT GTGTAGTATG AGTTACTATT CATGTTTCAG 720
CATGCATGCC CCTTACTGGT TCTGAAGAAC ACAATGGTCT TTGGTTACCA AGATACAAGT 780
AAACAATTGA AGATTACTTT TGGGTGTTCC TACACTGATG AACAATCCTG TGTGTTTTTA 840
TCTCCCTAGA TAATTTTAAT GATCTGGAAT GCTCTTAATG ACCTAATTTG GGGCTGGGCA 900
TTCATACCTA TAATCCCAGC ACTTTGGGAG GCTGAGGTGG GAGGATTGCT TGAGCTTAGG 960
AGTTTGAGAC CAGCCTAGGC AACATAGTGA GATCCCAGTC TCTACAAAAT ATGCTTTTTT 1020
TTCCTTTTTT TTTTTTTGAG ACAGAGTCTC TCTCTGTCGC CTAGGCTGGA CTGCAGTGGC 1080
GCGATCTCGG CTCACTGCAA GCTCCGCCTC CTGGGTTCAC GCCCTTCTCC 1130
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