Tag | Content |
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EnhancerAtlas ID | HS053-02703 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr1:157372630-157373740 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:157373006-157373024 | GCTGCCTTCCTTCCCTCT | - | 6.17 | EWSR1-FLI1 | MA0149.1 | chr1:157373002-157373020 | TCCTGCTGCCTTCCTTCC | - | 6.45 | ZNF263 | MA0528.1 | chr1:157373683-157373704 | CTTCCTCTCTCAGCCTCCTCC | - | 6.09 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I157402 | chr1 | 157372426 | 157374750 |
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Enhancer Sequence | GCAGGTGAGG GTGGTCCTCA ACTTGGGGGG ACCCCCTGAC CATAACAATA ACAGCACTTA 60 CTGAATGCCC ACTCCGTGTC TGCCAGCAGG GAGCTGGAAG AGAAAGGGTC TCTGCATTAG 120 GGGCTCCAGA CGCAGACACG AGACAATGGA GATGGCACCA AGAAGTGAGG TTTGGACATC 180 AAACATGAAT GGTTGGTTTG TGAGTGTGCT GATGGGGGCT ATGTCAGACA AATGAGCAAT 240 CTTTTATGTT GTTTACAGAG CTTGAAATTG TATACAATTT AAATGAATGT TTAGCTCCAC 300 CTTGTAAATG ACCAACCACT CCCTGTCTTG TTCTCTCTTC TTCAGGATTA GCATCTCTGT 360 AGATCCAAGA ACTCCTGCTG CCTTCCTTCC CTCTCTGAGT CTTCCCTCAT CTTCCTCCTG 420 GCTGTGCTCA CCATCCAACT TCTGGGGCAG ATCCTTCCTA ACAGCCTGAG GGCGGAGCCT 480 CCTTTCTCCC TGGTTCCCTC ATCCAGGAAG TGAGCTTGTC CAGGCTGGCA GTTTAACCCT 540 CTGTTAGCCA GAAGTCCCTG CTCTGCACTG CCACTGAAAG TACCTGCTTC CCCTTTTCAG 600 AAGAGGGCAA TTGAGGTGGA GGCCGCGGCA GCTTCTCAGT CCTGCGGGGC TCAGACGACA 660 GTGCAGCTGA GCTAGTCTAG GGAGGGCAGG TGAAGGTGGA GGAGCTCACG GGCAGTATCC 720 TGCAGGGGAG GCCTTGGGCT GGGGGGTAAA GTAGGCTCCA GGTCTGGCTC TGCCCTCTGT 780 GACCCAGGAC AAGTCTACCC CCTAGAGAGT CCCTCCTCTG TTAAAGCAGG AGCTTGGGCA 840 GAATCACCCC AGTCCCCCTC AGCAGTGAGG CTCTGGGAGT TGGTGACTCC CGTGGCTCTA 900 CCAAGGTCTC TGCTCTGTCT CCCCATCCTG TCCTGTCCTA TCCTGTGGTC TGACAGGCAC 960 TGACAGCCAG TGAGCCTGTT TCAGGCTTCT TCAGAGAGAA GACTCTGGGT GTCCCTGTGG 1020 CCACTTCCTC AGCCCTTGAG GGAGGAAGGG ACCCTTCCTC TCTCAGCCTC CTCCACCTGA 1080 CCCTCTGCTT TCTCTGCCTC TGCTCCTAAG 1110
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