Tag | Content |
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EnhancerAtlas ID | HS116-15859 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr18:10542790-10543700 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GLI2 | MA0734.2 | chr18:10543226-10543241 | CAAGGTGTGTGGTCT | - | 6.55 | Nr2f6(var.2) | MA0728.1 | chr18:10542964-10542979 | GAGGTCAGAAGTTCA | + | 6.38 | RARA | MA0729.1 | chr18:10542964-10542982 | GAGGTCAGAAGTTCAAGA | + | 6.88 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr18 | 10543130 | 10543398 | chr18 | 10543305 | 10543529 |
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| Number: 1 | ID | Chromosome | Start | End |
GH18I010543 | chr18 | 10543130 | 10543398 |
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Enhancer Sequence | TTTGGAGAGT CAAAATTCAG AAGTGATTCG TAGTTTCATT TAGATTACAT CTGGGAAAAG 60 TCAGTCCAAG GCCAGTGCCC TTGTTCCTTT TTAGAAAAGG CCTTTCCAGG CTGGGTGCAG 120 TGGCTCATGC CTGTAATCAC AACACTTTGG GAGGCTGAGG CAGGCAGATC ACCTGAGGTC 180 AGAAGTTCAA GATTAGCCTT GGCCAAATGG TGAAACTCCT TCTCTACTAA AAATACAAAA 240 AGTAGCCGGG TGTGATGACG CACACCTATA ATCCCAGCTA CTCGGGAGGC TGGAGAATCG 300 CTTGAACCCA GGAGGCACAG GTTGCAGTGA GACTCCCATC TCAAAAAAAA AAAAAAAGAA 360 AAGAAAAGAA AAAAAGACCT TTCCAGCAAG TTGATCATGA CCTTGTGCCT CTGAGAGAAG 420 GTCTATGCCT CTGAGACAAG GTGTGTGGTC TCAGTGAACC CAAATCCCTC CTAGAAGACT 480 CACTTAGCAA AGAAAAGAGC TGCTTCTCAC CAGTTGTCTG AGACAGTCAC TAGATCCTAA 540 ACACAAGGAG GGTTGGGTGT GTATATGTTC AGGGGTGGGA TGTGTGCTAT TAAGGAGAAT 600 CACTGGGTTT CTGTCTTGCA TAACTGTTCT GTCCATGGTG CCATCAATAA CTGAGATAAG 660 GAATATAGAA ACAAACTTAT CAGTGATGAT AATAAACTTA GCTGGGAATA TGACACATAA 720 ACTAAACATT TCTGTAGGTA GTTAAAAATA GGTTTTGGAG TTCAGGAAAT AGTTGGGGCC 780 AGAGGAACAG TTTGAGTTGT GGTGTAGAAG GTGTCTGTTG AAAGCTTGGG GATGAATGAG 840 GTTCTGTGAC AGTTTTCTGC CATTTGCACA TAACTTCTGT GGGGTTTCAA TTTTGTTACA 900 TTTGGGGAAG 910
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