Tag | Content |
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EnhancerAtlas ID | HS066-02865 |
Organism | Homo sapiens |
Tissue/cell | GM18516 |
Coordinate | chr19:40424940-40426460 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gata4 | MA0482.1 | chr19:40426076-40426087 | AGGAGATAAGA | - | 6.14 | Nr2f6(var.2) | MA0728.1 | chr19:40426307-40426322 | TGAACTCCTGACCTC | - | 6.22 | Nr5a2 | MA0505.1 | chr19:40425602-40425617 | AAAGTCAAGGCCAGG | + | 6.14 | Nr5a2 | MA0505.1 | chr19:40425443-40425458 | CCTGGCCTTGAGCTG | - | 6.31 | TFAP2C | MA0524.2 | chr19:40426101-40426113 | TGCCCTGGGGCA | + | 6.44 | TFAP2C | MA0524.2 | chr19:40426101-40426113 | TGCCCTGGGGCA | - | 7.22 |
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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 |
GH19I039920 | chr19 | 40425961 | 40426070 |
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Enhancer Sequence | TGAGGCGGGT GGATCACTTT ATGTCAGGAG TTTGAGACCA GCCTGGTCAA CATGGTGAAA 60 CCCTGTCTCT ACTAAAAATA AAAAAATTAG CTGGGTGTGG TGGGGCACGC CTGTAATCCC 120 AGCTACTCAG TTGGCTGGGG CAGGAGAATT GCTTTAACCC AGGAGGTGGA GGCTGCAGTG 180 AGCCAAGATC GTGCCAAACA GAGTGAGACT CTGTCTAAAA AAAAAAAAAA GGCAGCCTCT 240 CCCTATTCCA TAGCCTCCTT CCCTGCTTTC CTTTTTTTTC TATAGCATCT GGCCTTCTGA 300 AATATAATTC ACAAATTGAC CATGTTTATC ATCTGTCTTA CTCCATCAGA ATGGCAGCTC 360 CACAAAGACA AGGGTTTGGG TCTGCTTTGA TCACTGCTTT ATCCCCAGTG CATAGAACAG 420 GGCCTGGTAG AATCCCAGGC ACTCACTAAG TGAATTAAGT CACTGCTGCA TTTAATAAAC 480 ATTCACTGGG CACTCACTCT GTGCCTGGCC TTGAGCTGGG AGATCCTGGG AATACGAAGG 540 TGGCGGAGAC AGCCCCAAGC CCTACCCTCA TGGGGCTCCC AGTCCATTGG GAGAAACAGA 600 CACATCACCA GACAGTGAGA GCTCAGAGGG GTCAGGGCAG AGATGGGAGA AGCACAGGCA 660 GAAAAGTCAA GGCCAGGATC AGAAAGGCCC AGGCAGAGGG GTCAAGGATG GGATAGGGGA 720 GGTACAGGCT GAGGGTTCAG AGCTGGGATA GTGGGGAGAT AGGAGGCTGT GAAAACCTAG 780 AAAAATGGCC AGATCTAACC TTGCTGGTCA GGGATGTTGA AATCTTAACA CCCAACATGA 840 TGGTATTAAG AGTGGGGGGA GGCCTTTGGG AGGTGATTAG GTCATGAGGG TGGCACCCTC 900 ATGAATGGGA TTAGTGCCCT TATGACAGAG GCCTCAGAGA GCTCTCAGAT CCGCTTTCCA 960 CCGTGTGAGG ATACAAGGAG AAGTAGGCCA TCTGCAACCT GGAAGAGCAC CCTCACCTGA 1020 ACCTGGCAGT GCTGGTGACC TCATCTTGGA CTTCCAGCCT CCAGAACACA GAGACGAGGT 1080 TGTGTTGTTT ATAAGCCTCC CAGGCTCTGG AGAAGCCTGA AGTCTGACTA AGAACCAGGA 1140 GATAAGAACT ATGTCTCTCT GTGCCCTGGG GCATCTTTTT TTTGAGATGG AATCTTGCTC 1200 TGTCACCAAG GCTGGGCTGC ATTGGCACGA TCTCGGTTCA CTGCAACCTC TGTCTCCCAG 1260 GTTCAAGTGA TTCTCCCACC TGGGATTACA GGTGCCTGCT ACCACGTCCA GCTAATTTTT 1320 GTATTTTTAG TAGAGATAGG GTTTCACCAT GTTGGCCAGA CTGGTCTTGA ACTCCTGACC 1380 TCAAGTGATC TGCCCACCCC TGCTCAGCCT CCCAAAGTGC TGGGATTACA GGCATGAGCC 1440 ACCGTACCCA GCCTTTTTTT TTTTTAATTA ATAAAAAAAT TTTTTAAATT AGATATGGGG 1500 GTCTCACTAT GTTGTCCAGG 1520
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