| Tag | Content |
|---|
EnhancerAtlas ID | HS184-22607 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr4:24975080-24976050 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TFAP2A | MA0003.3 | chr4:24975154-24975165 | TGCCTGAGGCT | - | 6.32 |
| | | 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 |
| GH04I024973 | chr4 | 24974653 | 24976822 |
| Enhancer Sequence | AATAAAGTGC ATTTAAAAAA AGTCTGGAGA AAAAGAAGTC CCCTTTTGTT TGCACTTGGA 60
GCTGTGATTA AGCATGCCTG AGGCTACTGG CAGCTATCTT GACATTGTGA GGAGAAAACA 120
TGCTTGAGAG TGAGGCCAAC CCAGAGGATA AAAAGAACTG AAAAAGGCCA GAGTTAGACC 180
AGATTCCAGC CATCCATCGG TACTGGATCC AGCTGTGCCT ACAGCAGTCT CTGGAATTTT 240
TGCTCATTGA GACAATACGT GTGTGTGAGT GTATGATTAA CCCGGTCTGA ACTGAGTTTT 300
GTTGGTTACA ACTGAGGAGT TCTGTGCAAC GTTATCCACA GTCCACCAGG CAGGCTGAGA 360
GCTGCTTCTT AACCAGCAAG TGCCTCATGG AGGGATTGGG TTTGGGGTTA TGGAAGTGAA 420
CAGAGCTGCC TGCCTTAAGG CAAGTAGGCC TTGCTCTGTT CCCCTTGCAG TCCCCGAGCC 480
CGGGAAGCCC GAGAGGGAGC CCTTCAGTGC TTGTGCACTC GGCTGTTTCG CAAGAGTCAC 540
GGTCAGTTGC GCCTCTGCTT CGGAAGAGTA TTTTTAGTGG CAAATAAAGT GGTGCGCAAA 600
TAAACAAACG CCTGGAACAA ATCCTGCAAA GGAGAGCGCC TGTGTGCGGC CCACTGTCTA 660
ACTAGGTCAG CCTCGGGCAC AGCTCCTTTT GACAGTTTGC TCCCCAGGGC GGAAGGTGAC 720
CCGCAGGTGC CGGCTGCTTT CCCCACCAAT CAGCCATCTG TGGTTTGAGA CTCACAAGCT 780
TAGGAGAGAC TCGGGAGGCA TCAGTTCCGC ATCCCGCACT CCCACGTGAA TTTGCCCCCG 840
CCCTGAGTCA GAACCCTAGA GGGGTGAAAT CCCTGAATTC TGCAGAGGAA ACCCATACTT 900
CTTTGCTTTT TCAGCAATTC CAGGAGATGT CGTTTTTCAA GTGGCAAATG TGTGGCTCTA 960
GAGGACAGAG 970
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