Tag | Content |
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EnhancerAtlas ID | HS052-39510 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr9:128136270-128137510 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr9:128137171-128137190 | GGGTGACATCTTGTGGCCA | - | 6.09 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr9 | 128136410 | 128137140 | chr9 | 128136627 | 128137500 |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I125374 | chr9 | 128136680 | 128137462 |
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Enhancer Sequence | TTCCCCTCCA GCCAGCCCCA CTCCAGCCAC TGAGAACTAT CACCTTTCCC AAAGTGCTGC 60 CCTTTGCCGG CCTCTAAGCC TTTGCTGATG CCCAGATCTG ACTGCCTCCC CCACAGTCCT 120 TCCTCCTGCC TCAGATGGCC CTTCTGGAGG AAAACCCCAG GTGCCCCCTC CTGCCTCCCT 180 CCTCAGTGAG GCCTCACCCC CATCCCTCCC TCTCCAGAGC AGTGTCTCCC TGGAGCCTGT 240 GCTCCTAGGG GAGGGCATGC CTCCAAATGG CAGGTGTCCC TAATGTTTGC AGATGGGGAT 300 GGATGAGAGG CAGAAAGTAG CCCTTCAGGG CGGGGATTCC ACCATCTTTT CCTTCCAAAT 360 TCAGGCCCTG CTGGGACAGG AACTATCCCT GTCGTGGTCC AGGGCCAGGT AGTTCTTCAC 420 GTCCTCTGGG AAGACAGAGT GCCCCAAAGC CCTTGATCTC CAGTGGGTAG AATTAGGTGG 480 GGCAGAGGCT GTGCCACACC AGGTCACACC TCTCCTGTGT CTGCTCCCAC CCCACCAAGC 540 ACAGGGCCGG GATGAGGATG CCTGGAGCCC AGCTCAGTGC CTGCCTGGGT TGCAGCCCTG 600 ATCACACCAA AGTGTCTTGT CTGTTTGCAG CCCTTTATCT GGCTAGCAGG GTTTAATTTT 660 ACTCTGGGAA GGTGGGATTT TTGTCCCTAT TTACTTATTA TTTTCGAATT TATTATCTTT 720 AGGTGGCATC TACAAATCGG CGTCCTCTGA GGGCAACAGC GCCCCGTTCT GCTAGAAATC 780 CCGAGATTTG CAGCCACTGC AGCACGCTGC CTCTGCGGCT TCTCCGCACC ATCCCCGACC 840 CCTTCCCCCG CGAGTCTGCC GTCGGCCAGT TTCCTCCCAG GCCCCGGCTT TGCTGTTCCT 900 TGGGTGACAT CTTGTGGCCA AGGACAGGTA CAAACCATTG GCTGAAAAGG AGGAGCAAAG 960 GCAGCCCTCA GCCCTCTCTG GAGGAGCCTT GGGGCGCCTT CGAGGATGCC CAGGAGGGCA 1020 GGGGGCTCCT GAACAGGGAA TCGGCTCTCA GACCCCGAAT GGGCTTGCAC CAAGCCCTTC 1080 ATGAGACAGC TGTGGCTGGA GCCCAGAATT CACCCAGGCC CCCCGAGGCA GACACACCAG 1140 GTTCCTCTCT GCCCACCCTG CGTTGTGGCA AATAATCATT ATTCCCGATA TAAAGCTTTT 1200 CTCTAGCAGC CCAACGACAA GGTTATTATT CCAATCTTAC 1240
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