Tag | Content |
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EnhancerAtlas ID | HS047-17551 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr19:40425220-40426200 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gata4 | MA0482.1 | chr19:40426076-40426087 | AGGAGATAAGA | - | 6.14 | 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 | TATAGCATCT GGCCTTCTGA AATATAATTC ACAAATTGAC CATGTTTATC ATCTGTCTTA 60 CTCCATCAGA ATGGCAGCTC CACAAAGACA AGGGTTTGGG TCTGCTTTGA TCACTGCTTT 120 ATCCCCAGTG CATAGAACAG GGCCTGGTAG AATCCCAGGC ACTCACTAAG TGAATTAAGT 180 CACTGCTGCA TTTAATAAAC ATTCACTGGG CACTCACTCT GTGCCTGGCC TTGAGCTGGG 240 AGATCCTGGG AATACGAAGG TGGCGGAGAC AGCCCCAAGC CCTACCCTCA TGGGGCTCCC 300 AGTCCATTGG GAGAAACAGA CACATCACCA GACAGTGAGA GCTCAGAGGG GTCAGGGCAG 360 AGATGGGAGA AGCACAGGCA GAAAAGTCAA GGCCAGGATC AGAAAGGCCC AGGCAGAGGG 420 GTCAAGGATG GGATAGGGGA GGTACAGGCT GAGGGTTCAG AGCTGGGATA GTGGGGAGAT 480 AGGAGGCTGT GAAAACCTAG AAAAATGGCC AGATCTAACC TTGCTGGTCA GGGATGTTGA 540 AATCTTAACA CCCAACATGA TGGTATTAAG AGTGGGGGGA GGCCTTTGGG AGGTGATTAG 600 GTCATGAGGG TGGCACCCTC ATGAATGGGA TTAGTGCCCT TATGACAGAG GCCTCAGAGA 660 GCTCTCAGAT CCGCTTTCCA CCGTGTGAGG ATACAAGGAG AAGTAGGCCA TCTGCAACCT 720 GGAAGAGCAC CCTCACCTGA ACCTGGCAGT GCTGGTGACC TCATCTTGGA CTTCCAGCCT 780 CCAGAACACA GAGACGAGGT TGTGTTGTTT ATAAGCCTCC CAGGCTCTGG AGAAGCCTGA 840 AGTCTGACTA AGAACCAGGA GATAAGAACT ATGTCTCTCT GTGCCCTGGG GCATCTTTTT 900 TTTGAGATGG AATCTTGCTC TGTCACCAAG GCTGGGCTGC ATTGGCACGA TCTCGGTTCA 960 CTGCAACCTC TGTCTCCCAG 980
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