Tag | Content |
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EnhancerAtlas ID | HS094-19052 |
Organism | Homo sapiens |
Tissue/cell | hMADS-3 |
Coordinate | chr19:19178280-19179160 |
Target genes | Number: 14 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gfi1b | MA0483.1 | chr19:19178461-19178472 | TGCTGAGATTT | - | 6.32 | Nr2f6(var.2) | MA0728.1 | chr19:19178946-19178961 | GAGGTCAGGAGTTCA | + | 6.22 | POU2F2 | MA0507.1 | chr19:19178828-19178841 | TGCATTTGCATTT | + | 6.16 | Zfx | MA0146.2 | chr19:19178924-19178938 | GAGGCCGAGGCGGG | - | 6.01 |
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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 |
GH19I019066 | chr19 | 19177601 | 19179019 |
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Enhancer Sequence | TAGTTGGGAG GCTAAGGTGG AGAACTGCTT GAGCCCAGGA GTTCAATGCT GCAGTGAGCT 60 ATGATTGCAC CATTGCACTC CAGCCTGGGC AACAGAGCAA GACCCTGTTT TTCTGTTAAA 120 AAAAATTTTT TTTGAGTTCC TGCTCTGTGA AGCTTGTCCC TATAGCAGGG AGCAGTGGTG 180 GTGCTGAGAT TTTGGCTCAA GGTACCTCAA CAAGAACAGT TGCTAGAAGA ACCATTTAGC 240 TGTTGCTGAT TTTTTTTTTT TTCACTTGGG TCTAGGAAAA GAAAGATGAG GGCATCATGA 300 GAGATTGAGA CGAGTCAGAT GTTAAATCTG TCTGGGAAGC TGTTTCGAGA CTCTCTCCAA 360 TTGTCCAATT TCTCACCACT GGTGCCAGAT GGAGGGTGTC GTCATACTGA AGTCAGGCCT 420 CTGCCCACGT GTCATACAGT TTTTTTTGTC TGTCTCTTCT ATTTTGGCAG TTAGACATTA 480 AGAGGGGATT ATTGAGATAA TCAGAATCAT TCGCTCGTTT GGGTTTTGCA AGACAGAGCT 540 TTTAAAAGTG CATTTGCATT TTTTATTTTA AACATGAAAT ACTTCTTCAT AAAAAGTATA 600 TTGGCCGGGC ACAGTGGCTC ACACCTGTAA TCCCAGCACT TTGGGAGGCC GAGGCGGGCA 660 GATCATGAGG TCAGGAGTTC AAGACCAGCA TGACCAACAT GGTGAAACCC TGTCTCTACC 720 AAAGAATACA AAAATTAGCC AGGCGTAGTG GCATGCGCCT GTAATCCTAG CTACTCAGGA 780 AGCTGAGGCA GGAGAATTGC TTGAACCCGG GAGTTGGAGG TTGCAGTGAG CTGAGATCAC 840 ACCATCGCAC TCCAGCCTGG GCGACAGAGC GAGACTCTGT 880
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