Tag | Content |
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EnhancerAtlas ID | HS098-20036 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr15:74189290-74190820 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUN(var.2) | MA0489.1 | chr15:74190407-74190421 | CTGAGTCATCTCCC | - | 6.08 | NFE2L1 | MA0089.2 | chr15:74190403-74190418 | TCAGCTGAGTCATCT | - | 6.1 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr15 | 74190200 | 74190400 | chr15 | 74190400 | 74190464 |
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| Number: 1 | ID | Chromosome | Start | End |
GH15I073897 | chr15 | 74189741 | 74190879 |
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Enhancer Sequence | ATGTCAAGAT GTCAAGAAAT AGCCCATGAT AACTGGGCTG GGGAGATATT GACAAACGTC 60 TTCTCAGGGC AACTCAAAGC AATGGCCTCT TGTCACTTCC ATCCCATGGC TTGGATCCTC 120 TCCATTTCTC CATCATCCCC ACCTCATCTT GGTCGCCGCA CTGAAGGTCA CCAGAGCTGT 180 TTCCCTGAAT GTCCTCACAC CTCTCTTTCC CTCCTAGAAG GCCAGACCCT AAGTGGGCTG 240 CAGTGTGAAT TGGTTAGTCC TTGGACTCTG GAATCGGGCC CCAGGTAATA GTTGTGTGAC 300 CGTGGACAAT ATACTTAACC TCTTTGAGCC TCTGTTTTCT CACCTAGAAA TTAGAAATAA 360 CAATACCTGC CTTACAGGTT GTAATATGGC TATGTCTATG ATGCATTTAG CCCAGCAAAC 420 TTCGACTCAA AGAAATGGTA GCTGTTGGAA AGCCACAGAA GTAGTCAGGT TCAGAATTAA 480 CAGTTACTCT GTAACCCAAG AAGCTGTAGC CACAGGAGAG AGGACCTCTG CAGGATCTGT 540 GGCTTCCCAC AGCCACAAGG TGCAGCCTCC AGGGTGAGCC ACCTCCTCTT TCCTGTGGAG 600 CCTGCACTTG CGTGTGCCAG CCTACAGAGG GCGCTCCTCC TCCTCCACAA GCCCAGGACT 660 CCATGGGGAG GCCTGGCTGC CCCAGGGACC AGGCACCCTG CCCAGGTTGC AAGAGTCCTG 720 GGCAATCCCT GTGCTCTGGG GCAGAGGTGT TGCCGAGAGG GAGGAAGCCT AACTGGCTGG 780 CCCAGAGCTG CTTTGGGTCT GAAAGGGGGA CAGGGAGAAC TCTGTTGTTC ATGGCTCTCA 840 GAGGCCCTAC GCCTTGTACT CTAGCTGCAA ATTTGATGGG GAAGGAGCCT GGGACCAGGG 900 GAGCCTCGGG TTTCCCCGGA AGCATTTCCC AGCAGCCCTA GGACCCTGTG AGCAGGTGCA 960 GTGGGACCCA CGCGCCGCCT CTACTCCTCC TTTCCTGGCT GGGAATCCTT CCTGCCCCCC 1020 AGCACACACA CACATTCTCA GTGTAGTTCC GTGTGATTCA CTGTGAGTGG TCATCATCAT 1080 GGCCCGCATC ATGGCCTGAG GAGAGCAGGG ACCTCAGCTG AGTCATCTCC CCGAATGGTA 1140 ATGAGGGCAG TCTGGAGAGG ATCTGTCCTT CAGCCTCCTC CCTGGGTTCT CGGTCTCCAA 1200 CCCCTCACCA TGCGCAGGCT CACCCAGGGA GCTGCTGCTT CACCAGCAGG GAACTGCTCT 1260 GCCTCACCAG GCCCGTGTGG CACAGGGTGC AGCTGTGCAA GCCATGCCCT CTGGCCACAG 1320 GGCAGGTCAT TAGGCCAGCA CTCATCCCCT GCCACGGTCA GGGCTGTGTG GGGCTGGAAT 1380 CAGAGGCCTC CTCCGTTTCC TCAACCTGAT TCCTAAACAT TACCTGTTTC ACTGTGAAAA 1440 ACCATCCACG GACCTCTCCT GTGGTTTTCT ACGCCCAAGA CCAGCAGTGT TCAGTAGAAA 1500 CAGAATGTGA GTGAACCACA ATGTATTTTA 1530
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