Tag | Content |
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EnhancerAtlas ID | HS105-49669 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr20:31340060-31341000 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gata4 | MA0482.1 | chr20:31340379-31340390 | AGGAGATAAGA | - | 6.14 | Nr2f6(var.2) | MA0728.1 | chr20:31340951-31340966 | GAGGTCAGGAGTTCA | + | 6.22 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_32784 | chr20:31338120-31340990 | H1 | SE_68812 | chr20:31339660-31340703 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH20I032748 | chr20 | 31336645 | 31341024 |
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Enhancer Sequence | TTATATGAAG AGTCACGGAA AGACATTGCA AAGGAGAAAA ATGCTAGGAA GGAGAGTGGG 60 GGGCTGTCAA CAGGTGTAAT GGGGGTAAAC CTGTCCGGCG GAGGGAAGGT AAGCAGATGG 120 AGCAGTTAGC CTCTGTGGGG CCTTAGGAAA GGAGCAATTG AGGGGGAAGC CCTGGGGTCT 180 TGGGCATGTC ACCCCTACCT TCTCCCTCTA CTCTGCAGGT CAGCATAACT TGGTAATCAT 240 TTCCTGGCCT GCAGCCAGGG TTATCAGCAT GCTGTGTATA TGGACGTCGT GAAGATTGGA 300 GGCTGAGGGC CCTGACCAGA GGAGATAAGA ACAGGTTTGG ACAAGAAGAA TCCATCCCCT 360 CTATGTTTAT CTCAAAACGG TAGAGCAGGC TGAGTCTGGA CCCAGAACAA ATCCAGGAAG 420 TAGAATCCAA GAAGCAGAGA GATGAATCAA GAATGACACT AAGGTTTTGG GCTTCATTCC 480 ATGCTACACT ATCTGCCCCA TTTGACAGTG AAGGAAGCAG ACGCCCAGAG AAGGGAAGAC 540 ACCTGTCTGA GGTCACACAG TGGGTTAATA GGAGAATGAG AACAGAACCT AGACCGCTGA 600 ACTTTTCCCC TTAACCATCT TACCCTCCTC AGAAGTCAAG CCTGAGCTTC CAAAAATGAA 660 GGAACTCAGG TCCAGGGAAA CTTTCTGTTT TGTCTGAGGG TGAGGGATGA GATAATGATG 720 AGTCAGGGCT TCAGGGAAAC GAACATTTAC TGATTACCTA ATGTGGGGGT AGATGTGGTC 780 CCTGCTCTCA GAAAGCTCAA AGTGTGAATG AATTAAAGTC AATGTGACCA GGCGCGGTGG 840 CTCATGCCTA AAATCCCAGC ACTTTGGGAG GCCGAGGCAG GCAGATCACC TGAGGTCAGG 900 AGTTCAAGAC CAGCCTGGTG AACATGGTGA AACCCCATCT 940
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