Tag | Content |
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EnhancerAtlas ID | HS098-39929 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr3:127813960-127814790 |
SNPs | Number: 2 | 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 | chr3:127814152-127814171 | TCCCCAGCAGGGGGCACCA | + | 7 | Nr5a2 | MA0505.1 | chr3:127814005-127814020 | GAGATCAAGGCCACC | + | 6.05 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_41754 | chr3:127813796-127815422 | LNCaP |
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| 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 |
GH03I128094 | chr3 | 127813601 | 127815262 |
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Enhancer Sequence | CGGGTCTCAG GCTGACCAGA GCTTTGTCTC CACTGAGCAG GTTCTGAGAT CAAGGCCACC 60 TTTCTGTGCA CCTTAGTCCT GAGTGGGATG GGACTGAGAG ACCTTACTTC TGAGACGAGA 120 GATGCCAGGC TCTGCAGGTA TGGGCTGGGC TGGGTTCCCT ACTGTGGAGG GAGGGAAGCC 180 TATTAGCAGA GCTCCCCAGC AGGGGGCACC ATCTGTCCAA GGCTGAGCCC TTTCACCAAC 240 TGCACTGTCA GGCTTCAGCC TGGCCTAGCC AAGGCTAAGC AAGTCCAGAC AGCCACAGGC 300 ATGCCAGGCA TACCAGCCAT AAGGCCCACA TGCATCTGTC TCCAGAAGCT GCCCAAGTAG 360 CCATGCTGGA TCTGGCACAC ACTTTCTCTC CAAGACTTAG GAAGCACTTA TGACAGTGGT 420 CTTGTCTAGA GAGCATCACG GACGGGGATT CAGAGTAGCT ACAAGATGCT GCCACATGGA 480 CTTGAATCAC GCATTCGATT CCTAATTGCA AGTGAAAGAA ACCGCCTGAG GGGGAAGGGC 540 TGTTGCTATA CTGCAGTGCT CACAGCACTA CAGAACCCCC ATTGTGGGGC TTACCCAGAG 600 CCAGCAACAC CAGAGTTTGC ATGTTTTGTT TTTTTTTAAT TATTTTTAGA GATGAGGTCT 660 CACTGTTGTC CAGGTGGGAG TGCGATAGCT ATTCACAGGT GCAATCATTG CACACTACAA 720 CCTTAAACTC CTAGCCTCAA GCAATCTTCC CGCCTCAGCC TCCCAGAGAG TACACTACAG 780 GTGCATACCA CTGTGCCCAG CTTGGACAGT CTTAATAATA AAGCTTCTCT 830
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