Tag | Content |
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EnhancerAtlas ID | HS139-29834 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr2:113483460-113485040 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr2:113483790-113483809 | CACTGACCCCTGGTGGCTT | - | 6.06 | CTCF | MA0139.1 | chr2:113484468-113484487 | CAGCGCCCTCTGCTGGCCG | - | 8.57 |
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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 |
GH02I112724 | chr2 | 113482377 | 113485050 |
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Enhancer Sequence | AGGTACACAC CTTCCACCCA GGTATGACTT GAAGTCATCC TCCAGGGCAG GGAGTTGTGT 60 GAGCCCACAC AATTTGGGCT TTGTCCTGAG AGCTGAGGCT TTAGGTTTGA GTCATTGCCG 120 TGTGACCTCA GGAAGGTCAC CTGACTCCCT CACCTGTCCC ATGGGGCCTA CGGGGCCTAT 180 GCTGTCCCTG CCTCAGTCTG GGCAGAGTCT CACGTGATGT AAGGGGCCAG GGGTGTTATG 240 CACACAGCTC AGGGTGTGCA AGTCCTCCGC TGGGCCAGGG CAGACACAGG CAGGCAGGGC 300 CAGTGGGTGA CACAGGCCGT CACTCACCCC CACTGACCCC TGGTGGCTTT TCAGAGCGGT 360 TGGAGGAGCT GAAGAGACTG GACACGCACC TGGCAGACAT ATACCAGTGA GACCCTGGCC 420 TTTCTGGGGG TGGGATGGGG CAGGGAGAGG TATGGAGGGG CAGTGGCTCA CATCCCTGCC 480 TGGCGGCGAG GTCCCGGCCA AGGTTGTCAG AACATCAAGA TCTGTTTCAG GCTGGGCTTC 540 CCTAGCAAAC TGAATGTGGG GACCCCTCTC ACCCCCTTGG GACTGCTCAC ACTCTGTGAC 600 CTCTAGGCCC TTCCTCTGAA CCTATCCAGC ACTCAGGGAC CTGCCCTCGC ACGCATGCAC 660 ACACCCAGCC CGGCACCCCC ACTGGATGCC CGCACGGTGT CCCCCCACCC GACCCCTGCT 720 GGGGTCTAAG GAGACTGTCC TGGCACTCGG AGGCTCTGTG CCTCCCCTGG GTCACCTAGC 780 TATTTTTGTA CCAGGCACAT GGATGGGAGC AGTTGTGAGC TGCAAGTCAT CAACTTCACC 840 AAGAGAGAGA TCCAGGTGGG AGCTGGGTGG CGAGGGAAGG GACAGGCCCA GCAGGGGCGG 900 AGCCGGGTTC ACTTCCCCAC TGCTTGCCTG TCGGCTTTGT CCTCGGTGCC AAAGGCCCAG 960 TTACCCCATT CTCCTCAGCC TCGCCTGGGC TCCACCTGCC TTGTCAGCCA GCGCCCTCTG 1020 CTGGCCGACA TTCCAAAGGG CAGCGGTACC CTCTTGAAGG GCTGAGTTGA GCCTGATTTG 1080 CAGGCTTTGC CTCCAGTCCC ACAGTCTTTG CCAATCACCC TGCCCGGGAA GTGCCTGCGT 1140 GCTAGCTGGG CCCTTATTGA CTGACTAGCC AGTTCTGATA GGAAATGTGA TTTAGGGCCA 1200 GTGAGCCCAG GGTCCTTGGA AAAGAGAAGA AAAGACAGTG TTCCCTTGTG GCATTACTGA 1260 CCGGCCACCA AAAAGCTGGA GGTGCCCATG GGTCAGCCAG GTGGAGGGAG TCAGGTCACT 1320 TGGTCATCCC AAGCCCAGCT GGGGCCGATC ACAAAGGGTC TTTGCAGAGC CTTTTACAAA 1380 GCACAGCCGT TTGATCTTCC CCACAGCCTT AAGAGGTGGA TGGAGCAGGG ATTGTCACCT 1440 TTATTTTACA GATGAGGAAA CTGAGGCTCA GAGAGAGGTC ATCCTGGGAG TAAATGTTGG 1500 AACCATTCTC TAGGCTCTAA AAGCAGACAG GAAACAGGGC CTGGTGGCGG GGTGGGGCCT 1560 GCCAGGATAG TAGGAGCGAG 1580
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