| Tag | Content |
|---|
EnhancerAtlas ID | HS062-00084 | Organism | Homo sapiens | Tissue/cell | GM18486 | Coordinate | chr1:9555010-9555980 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:9555463-9555482 | CGGCCACCAGGGGGCGCAG | + | 8.39 |
| | | 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 |
| GH01I009494 | chr1 | 9554958 | 9555859 |
| Enhancer Sequence | CTCATAGAGG GAGGGTCCTG GGAGGGGGCC TCTCTGCATT CCCCACCCTG GCAGCTCTGG 60
TTTAGTGAGT GGATGGGCTA CCCTGGGCTG CTGTGGGCAT TCCGGGGGGA GGAGGTTTGC 120
CTCTCTCCGC CGCTTGGGGT GTGTCCTGGG AGAGCCGGAG GGGCAGAGCG GGGAGGGGAG 180
GGGCTTGGTC TTCGTCCTGG GTAAGGTTGG TAGTGGCTGG GTAAAGGGCT TTAGGCTACC 240
ATCTTCCAGA GGGGCCACCA AGGGTCCCCC AATCTGGTCC TGGGGATGGT GGCTCAGGAC 300
CCTCGAGAAA GCAGGCGGGG AGAAAACTCA GCGTGGCTAC CATTGGGGAC CTTGATTAGT 360
AGGTCATACC GCAGTGCCCA CCGCAAGGGT GGCCACTGCG GACGCGAGGG CAGCCCCGCC 420
TCAAGTAGCG CCCCAGAGCG GCCACTCCTC GTGCGGCCAC CAGGGGGCGC AGCAGCGCCG 480
GCAGGAAGCG CGGGAAAGCG GCCGCGATGG CCTCGGAAGA GGATGCGCCC CGCGCCGCCC 540
GCCCTGCGCC ATGCACTGTT ACCCCTCGGT CCTCACCCGC ACTGCGGGTG CGGGGTGGCA 600
ACTACCCCAG CTGGATAGTG AGGGTGCCGG GACGCAAGCC CGGGGCAGGC TCTCAACTGC 660
CCCCGCCCTT GCTTCTCAGT CGCCCTGCAC ACAGCCTCCC CCGAAACCAA AATCCCCCAG 720
GAGAGTGTGG TACCTCCATT ACAGTCGACA CGTCATTGTC ACTAAAGTCA GAGCTGACAC 780
CGGAGCTCAC TCCTGGTAGT GTTCATTCTA CGGGCTTTGA CAAATGTGAA ATGCATTATG 840
GCGTGCATCT ACTATTGTAG CGGCATAAGA ATAGTTAGAC TGCCCGAAAA ATCCCGTGTT 900
CTTTGCCTGT TCACCCCTCC CTACCACCCC CAACCCCTGG CCACCACTGA ACTATTTACT 960
GTCTCCACAG 970
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