| Tag | Content |
|---|
EnhancerAtlas ID | HS052-00213 | Organism | Homo sapiens | Tissue/cell | Fibroblast_foreskin | Coordinate | chr1:9554940-9556130 | 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 | CACCTCTGCG TGTCTTAACA CTCAGCCTCC CTCAAAAACC AGGTGGCAGA GCCCTTCCCT 60
GGTCTTCTCG CTCATAGAGG GAGGGTCCTG GGAGGGGGCC TCTCTGCATT CCCCACCCTG 120
GCAGCTCTGG TTTAGTGAGT GGATGGGCTA CCCTGGGCTG CTGTGGGCAT TCCGGGGGGA 180
GGAGGTTTGC CTCTCTCCGC CGCTTGGGGT GTGTCCTGGG AGAGCCGGAG GGGCAGAGCG 240
GGGAGGGGAG GGGCTTGGTC TTCGTCCTGG GTAAGGTTGG TAGTGGCTGG GTAAAGGGCT 300
TTAGGCTACC ATCTTCCAGA GGGGCCACCA AGGGTCCCCC AATCTGGTCC TGGGGATGGT 360
GGCTCAGGAC CCTCGAGAAA GCAGGCGGGG AGAAAACTCA GCGTGGCTAC CATTGGGGAC 420
CTTGATTAGT AGGTCATACC GCAGTGCCCA CCGCAAGGGT GGCCACTGCG GACGCGAGGG 480
CAGCCCCGCC TCAAGTAGCG CCCCAGAGCG GCCACTCCTC GTGCGGCCAC CAGGGGGCGC 540
AGCAGCGCCG GCAGGAAGCG CGGGAAAGCG GCCGCGATGG CCTCGGAAGA GGATGCGCCC 600
CGCGCCGCCC GCCCTGCGCC ATGCACTGTT ACCCCTCGGT CCTCACCCGC ACTGCGGGTG 660
CGGGGTGGCA ACTACCCCAG CTGGATAGTG AGGGTGCCGG GACGCAAGCC CGGGGCAGGC 720
TCTCAACTGC CCCCGCCCTT GCTTCTCAGT CGCCCTGCAC ACAGCCTCCC CCGAAACCAA 780
AATCCCCCAG GAGAGTGTGG TACCTCCATT ACAGTCGACA CGTCATTGTC ACTAAAGTCA 840
GAGCTGACAC CGGAGCTCAC TCCTGGTAGT GTTCATTCTA CGGGCTTTGA CAAATGTGAA 900
ATGCATTATG GCGTGCATCT ACTATTGTAG CGGCATAAGA ATAGTTAGAC TGCCCGAAAA 960
ATCCCGTGTT CTTTGCCTGT TCACCCCTCC CTACCACCCC CAACCCCTGG CCACCACTGA 1020
ACTATTTACT GTCTCCACAG TGTCGTCTTT TGCAGAATGT CACATAGCTG GAATCATGCA 1080
GCATGTAGGC TCTTCAGACT GGCCTCTTTC ACTAGTGATA CGCACTCAAG CTTCCTTCTG 1140
TCTTTTCTTG ACTTGCTAGC TCATTTCTTT TCAGCACTAA GTAATATTCC 1190
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