Tag | Content |
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EnhancerAtlas ID | HS146-00338 |
Organism | Homo sapiens |
Tissue/cell | NHDF |
Coordinate | chr1:29528640-29529610 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr1:29529549-29529568 | GGGCGCCCTCTGGTGGACA | - | 7.88 | NKX2-3 | MA0672.1 | chr1:29528887-29528897 | TTCAAGTGGT | - | 6.02 |
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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 |
GH01I029201 | chr1 | 29527693 | 29530110 |
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Enhancer Sequence | GAACCCGTGC TTCTTTTTGC AGGAAGCTGG GATTAGGTTT AAGCCAGGCT TGAGCAGGGA 60 CCAGCCACCT AATTTCATGC AGCTTCAATA GCTCTTGGCT GTCTCCTCAC TGGCAACAGA 120 GTGAGACTGG GTGGTTTTCA CAGGCCCTGA CAGCTCAATA GTGTTAGAAG CCATCTGTGC 180 CCAGGGAGAA GTCACTTAAC TTCCTGATTT CTTCTACTGA AAGGACAAAC TCCACTTCCC 240 CCCTCTTTTC AAGTGGTTCT TCAGAGTGTT GGACATACAC AGTCTAGACC AGGAGTGGCT 300 CTGGGTCTCT TTGGTTAAGG CAAATGGAAT TATTTTTGCG AGTACAACTG AGGAACTGAA 360 GCTGGTGTCG ATTATACTAA GAGTGGGCTT CCATGACAGC CACAGCCACA TTCATGGACA 420 GTGAGGCCTA GAGAAACTGG ACGATATGAT GGAAAGAGAG TAAGTGAGGA AACCGAGTCT 480 ATTACTGACT TGCTGTGTCT TCCAGGGCAA GCTGCTCCCT GAAACTTCAG TTTCCTCATC 540 TGTAAAAGAC AGATGACAAA CCTGCCCCTG TCTCCTTCAC GTCTGTATTT AGCGCACTTC 600 CAAGTACCAC ACAAAAGCAA GGGTAAAGGG GCCTTGGGTT AGACAGTTCA CAGAAAGAAT 660 AATACAGCTC AAATCATTCC CAAATATCAA CTGGGGTTTT GAAAACATGA GGTTATCACA 720 AGCCAAGAGT CTCAGAAAGT CTTAGCTATT CAGTAAGGGC AGTCTCCACC TCCTTCCTGC 780 CCTCTCTTTA CATGTCAGAT TCACTCATCC TATCGCCAAA AGCCAGCTGG ACTTCATTTC 840 TTAGGACTGA CTCATCTGTT TCAGCCGCCA ACTGTTAGCG ATGCCTAAAG CCAGTTTATG 900 CTTATGCAAG GGCGCCCTCT GGTGGACAAC TGGGCACCGC AGGGATGGGA GGTGGGAAAG 960 ACCCAAGACA 970
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