Tag | Content |
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EnhancerAtlas ID | HS047-00300 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr1:15294600-15296090 |
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) |
RARA(var.2) | MA0730.1 | chr1:15295068-15295085 | AGGACACGTGAGGGTCA | + | 6.03 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_26798 | chr1:15294684-15296104 | Esophagus | SE_53292 | chr1:15293321-15296336 | Spleen |
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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 |
GH01I014967 | chr1 | 15294172 | 15298701 |
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Enhancer Sequence | ATTCACCCTA ATGTAGAATC AGTGGGAGAC CTGAGCTTGT TTTCCTGCAA CTAGATGGTC 60 CCATCTAGGG GTGACGGGAG ACAGTGACAG ATCATCAGGC ATTAGATTCT AATAAGGAGC 120 ACGCAACCTG GATCCCTCAC ATGCGCAGTT CACAAGAGGG TTCGTGCTCC TATGAGAGTC 180 TAATGCCATC GCTGCTGATC AGACAGGAGG TGGAGCTCCG GCGGTAATGT GAGTGATGGG 240 GAGCAGCTGT AAATACAGAT GAAACTTCGC TCGCTCGCCC CTCACCTCCT GCTGTGCAGC 300 CTGCTTCCTA AGAGGCCAGG GACCAGTACC AGTCCATGGC CTGGGGCTTG GGGACCCCGT 360 GTGAAGCCAC TGCATTGTGT CACTTTGTTA CAACAAGAAT GGGAAACGAA CCAGGCCCTC 420 TCTTTCCCTG GACTTGGCAG CCCTAAACAC TGCCCTCTCT CAGGGCTTAG GACACGTGAG 480 GGTCATCTGT TTCCTTTAGA AACGCCTGCA GGGCACAGCA GCCAGCACGG GGCGGGTGGA 540 GTTAGCTAGC ACTGACTGAG CATGGAGCAG AAGAAAGGAT CCGGAGTTTC CTCTCCTTAC 600 TGGAAGGACT AAGGCCTGTG GGAGCCTTTT CCCTGCCACA GAGTGAGTCA CCTGCCTTAC 660 ACTGAAAGAA ACACAACTTT ATTATTTAAT TTGCTCATTC ACCAAATGTT CCCTGAAAGC 720 TTCCCTACCC CAAAGCTTGT GCCGATGCCT GTGGTTCAGA GCATTCCAGG CCCTGCTCAG 780 AGTCTAGGGA CATGCCTGAA ACCTACGACA CACTCAGTGT ACCTTACTTG AATCCTATTT 840 TTCCAAGTGG CCAACCAGGC CTGTAGATGA GAGTCTATCC CATAGGCATT CCTGCTTCAA 900 GGAGTTCTAG GCTGCAGAGA CTGTCTTAAG TCCAGCGGGG TCGGTGGGGC TGGAAGACTA 960 AAGCTCCCAG CAGGTGCAGC CATGCCCTGG CTGCCTTTGC AGATGTCACC AGGCCTGCAG 1020 ACAGTGGGGT AGTAGGTGGC CTGAGAGGCT GTTGAATAGA ACGATGTGTC ATCTGTGCTG 1080 GGGCGGCCAT GCCCACTTGC TTTCTTAGAC ACACATCCTT GTCACCACAG CACTGTGTGG 1140 GTTTGAAAAG CTACTTGATG TTTCCTGTGT CCCTTCCCAC ATCCGCACTC CATTCTTAGT 1200 CTCATTCCCT CCATCAAAGA CGTGTTCATC TTCTATGCAG TTCATCACCT GGGGTTGAAT 1260 GTGTATGTTC CTCTTTAGTA AATTCATACG CTTGAAGCTA CTGCTGTTTC TTTAGCCTGG 1320 TGGCTCTCGG GGCTGCTGCA GGGGGCCCAC CCTGAGCCAG CCCCTCGGTC CCACAGCCCT 1380 GACGTAGAAG ACTCTTTGCT GGTAAATCTC GGAACTCACT GGAAGCTTCC ACAAAGTTTA 1440 ACTCTACAGA CAGAATGTCT TCCTTACATA CTACCGGCTG CTTTTAAATA 1490
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