Tag | Content |
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EnhancerAtlas ID | HS060-23196 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr22:36593200-36594230 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RFX1 | MA0509.2 | chr22:36593337-36593353 | GGTTGCCATGGCAACT | - | 7.76 | RFX1 | MA0509.2 | chr22:36593337-36593353 | GGTTGCCATGGCAACT | + | 7.77 | RFX2 | MA0600.2 | chr22:36593337-36593353 | GGTTGCCATGGCAACT | - | 8.07 | RFX2 | MA0600.2 | chr22:36593337-36593353 | GGTTGCCATGGCAACT | + | 8.2 | RFX5 | MA0510.2 | chr22:36593337-36593353 | GGTTGCCATGGCAACT | + | 8.08 | RFX5 | MA0510.2 | chr22:36593337-36593353 | GGTTGCCATGGCAACT | - | 8.21 |
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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 |
GH22I036196 | chr22 | 36592046 | 36595470 |
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Enhancer Sequence | AGCCCAGCCC TTCCTAAGGA TTCTGGGATT GGCTGAGAGC TCTCAGCTTC TAATCTTCCC 60 TGCCCTCCCC TCATCTTGGA CAGGACTCAG CACAGCCCAG TTTGCTGTCC AGGGCGGCCC 120 CTGAGCAGAG CTGACTTGGT TGCCATGGCA ACTCTGTAAG GGGAGGAAGC CCTCCTGAGG 180 AAATGGGGCT TAGGGAAATG AACGCAGTGC TGACTTGGCT GGGCGAGGGA TTGTCTTGTT 240 TTTTCTTTTT CCTTCTTCAC CAAAAGGAGG AAGGAAACTC AGGGTTGGAT GGAGGGAACC 300 TCCAGCACTA AATTTGTGTT TTATTGATGG GGTGGGGATG GTGAATATTA AAGCAAAATT 360 AAAATAAAAA CCAGACCTGA AACATTCCCG GGCAAACAAA ACCAACCAGA CCTTCAGAAC 420 AGCTGTAACC CCCCATGAAA CTGCAAGCTA TGAATCTGAA CTGGGGTCAT ATCAGATGGG 480 CGCTTCTGTC AGACACAAAC ACAGCTTAAC CTCGGCCAGT CATGAGCAGC CAGCTGACAG 540 AGGGCCATGC TGAGATGTGG ATACTGGGAG GTCACAGAAA GAACAAGAAC TCCAGGCAGC 600 AGGTTCACAT AATGGACACA GAAGGAGCTG CTGTAACCAG CTGTAGGGAC AGGGGGAGGG 660 GATGGGCCCA GAGGACCCTG ACAAACAGGA AGTGGCCAAT CTGGCTAAGA CCAGTAAGAT 720 CTAACTCAGC ACTGGGTCTG ACCCACCTTT CACCCCAGAC TCAATCATAC CCTCCTTGTC 780 CCACACCCAC CTGTGCCACA GAAGTTCCAT GCTTGCAACA AAACTGCGTG GCCCCCCAGT 840 TCCAAGAAAT CCCCGCCTCT TCCCATAAAT CCTTATGCTT ACTCTGCCCC TTAACTTAGT 900 AAACCCACAA AGTCAGAAAC CCCAAACCCC ACTGGGCCCG ACTGGCTCTT CTGAGTCCGC 960 CTGCACTCCC ACCCCTGAGC CTGCGCTTCT GCTTTGCAAT AAAAGCTAAT TTGCTTTGGC 1020 TTTGCCTCAA 1030
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