Tag | Content |
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EnhancerAtlas ID | HS098-00514 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr1:15294260-15296300 |
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) |
BCL6B | MA0731.1 | chr1:15296255-15296272 | TGGATTCCTAAAAAGAA | - | 6.19 | NR2C2 | MA0504.1 | chr1:15294348-15294363 | AGACCTTTGACCTCC | - | 6.19 | Nr2f6 | MA0677.1 | chr1:15294348-15294362 | AGACCTTTGACCTC | - | 6.3 | RARA(var.2) | MA0730.1 | chr1:15295068-15295085 | AGGACACGTGAGGGTCA | + | 6.03 | RREB1 | MA0073.1 | chr1:15294491-15294511 | GGTTGGGGGATGGTTTTGGG | - | 6.25 | Rxra | MA0512.2 | chr1:15294348-15294362 | AGACCTTTGACCTC | - | 6.14 |
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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 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I014967 | chr1 | 15294172 | 15298701 |
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Enhancer Sequence | AAAGACAAGG AAACAGGCTT TCCCCAGAGC CTCCAGAAGA AAGGCAGTCC TGCCAACACC 60 AGGGTTTTAG CCCGGTAACA CCCATTTTAG ACCTTTGACC TCCAGAACTA CTATAAGAAC 120 ATTCATTTGT ATTAAATTAA TTTGTATTAT GTTAGGCCAG CAGTCCCCAA CCTTTTAGGC 180 ACCAGGGACC GGTTTCATGG AAGACAGTTT TTCCACGGAC CAGGTGTCCG GGGTTGGGGG 240 ATGGTTTTGG GATGATTCCA GGGCATTACA TGCACTACAT TTCTTGTGCA CTAAATTTCT 300 ATTATTATTA CATTGTAATA TATAGTGAAA TAATTATACA ATTCACCCTA ATGTAGAATC 360 AGTGGGAGAC CTGAGCTTGT TTTCCTGCAA CTAGATGGTC CCATCTAGGG GTGACGGGAG 420 ACAGTGACAG ATCATCAGGC ATTAGATTCT AATAAGGAGC ACGCAACCTG GATCCCTCAC 480 ATGCGCAGTT CACAAGAGGG TTCGTGCTCC TATGAGAGTC TAATGCCATC GCTGCTGATC 540 AGACAGGAGG TGGAGCTCCG GCGGTAATGT GAGTGATGGG GAGCAGCTGT AAATACAGAT 600 GAAACTTCGC TCGCTCGCCC CTCACCTCCT GCTGTGCAGC CTGCTTCCTA AGAGGCCAGG 660 GACCAGTACC AGTCCATGGC CTGGGGCTTG GGGACCCCGT GTGAAGCCAC TGCATTGTGT 720 CACTTTGTTA CAACAAGAAT GGGAAACGAA CCAGGCCCTC TCTTTCCCTG GACTTGGCAG 780 CCCTAAACAC TGCCCTCTCT CAGGGCTTAG GACACGTGAG GGTCATCTGT TTCCTTTAGA 840 AACGCCTGCA GGGCACAGCA GCCAGCACGG GGCGGGTGGA GTTAGCTAGC ACTGACTGAG 900 CATGGAGCAG AAGAAAGGAT CCGGAGTTTC CTCTCCTTAC TGGAAGGACT AAGGCCTGTG 960 GGAGCCTTTT CCCTGCCACA GAGTGAGTCA CCTGCCTTAC ACTGAAAGAA ACACAACTTT 1020 ATTATTTAAT TTGCTCATTC ACCAAATGTT CCCTGAAAGC TTCCCTACCC CAAAGCTTGT 1080 GCCGATGCCT GTGGTTCAGA GCATTCCAGG CCCTGCTCAG AGTCTAGGGA CATGCCTGAA 1140 ACCTACGACA CACTCAGTGT ACCTTACTTG AATCCTATTT TTCCAAGTGG CCAACCAGGC 1200 CTGTAGATGA GAGTCTATCC CATAGGCATT CCTGCTTCAA GGAGTTCTAG GCTGCAGAGA 1260 CTGTCTTAAG TCCAGCGGGG TCGGTGGGGC TGGAAGACTA AAGCTCCCAG CAGGTGCAGC 1320 CATGCCCTGG CTGCCTTTGC AGATGTCACC AGGCCTGCAG ACAGTGGGGT AGTAGGTGGC 1380 CTGAGAGGCT GTTGAATAGA ACGATGTGTC ATCTGTGCTG GGGCGGCCAT GCCCACTTGC 1440 TTTCTTAGAC ACACATCCTT GTCACCACAG CACTGTGTGG GTTTGAAAAG CTACTTGATG 1500 TTTCCTGTGT CCCTTCCCAC ATCCGCACTC CATTCTTAGT CTCATTCCCT CCATCAAAGA 1560 CGTGTTCATC TTCTATGCAG TTCATCACCT GGGGTTGAAT GTGTATGTTC CTCTTTAGTA 1620 AATTCATACG CTTGAAGCTA CTGCTGTTTC TTTAGCCTGG TGGCTCTCGG GGCTGCTGCA 1680 GGGGGCCCAC CCTGAGCCAG CCCCTCGGTC CCACAGCCCT GACGTAGAAG ACTCTTTGCT 1740 GGTAAATCTC GGAACTCACT GGAAGCTTCC ACAAAGTTTA ACTCTACAGA CAGAATGTCT 1800 TCCTTACATA CTACCGGCTG CTTTTAAATA TTGTTAACAG ATCCCCCTTA AAGGCTTCTT 1860 AGACTCCACA TTTTGATCCA GTTGATAATA ATTGATGGTC AGGTGGAAGA ATTGCCCAGG 1920 CTCTGTTGTT GTTCTGTTAT AGTTGCCACT GGACCTGCTT TCAGCACCCT CACCCTGGCT 1980 GCTTCAGAGG GCAGCTGGAT TCCTAAAAAG AACCCATGCC CTAATGCACA AGTACTTTTT 2040
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