Tag | Content |
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EnhancerAtlas ID | HS195-01720 |
Organism | Homo sapiens |
Tissue/cell | VCaP |
Coordinate | chr12:121664870-121665750 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr12:121665672-121665687 | GAGGTCAGGAGTTCA | + | 6.22 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_28089 | chr12:121664209-121668971 | Fetal_Intestine | SE_28761 | chr12:121664047-121669000 | Fetal_Intestine_Large |
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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 |
GH12I121226 | chr12 | 121664242 | 121668712 |
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Enhancer Sequence | ATTGCACTCC AGCCTGAGCA ACAGGAGCAA GACTCCATCT CAAAAAAAAA AAAAACCTGA 60 GAGAAGCCCC TTGGTCCCAG CCTTTCTCTG ACAGCAGTGG TGACAGGCTC AGCTCTCCTC 120 CGAGTGCAGC CCTGTCACTG ACCTTGCTCC TGTCTCAGGG CTGGGAAGAC TGTTGATGTT 180 GTCATTCCAA AGATCCCACC TGGATCAGGG GAACATCCCC CACAGAAGGG TTAGCCATAC 240 AGTGCCAGAT TCTCCAGGAG AAATTCACCA AAGAAATGGA GTCCCCTTGG GGACAGATTC 300 AACTTGTATT GTCAGCCAGG AGCTGACGTG GCACTTCTGA GAAGAGGCCG GCGCACCTGC 360 TGGCGGGTGC TTTGTGCACT TTTCAGACAG GTCAGGATCC AGCCTGTAGG CAAATTTACT 420 TTTGCTTTGA CCTGTAAAAC CGGATCTGCC CAGCCTTCAT TCTCTCCCTG GAGAACGCCT 480 GCGGCCCCAA AGCCAGGCCT ACTGATTTCC AGTGAGGCCA CAAATCCCCT CCCTGGTTAG 540 CAATTCAGTT TTCACCGCCT TGGGGGAGAG GGCCTGCCCT TCCTTGAGGG GAAGAACCTG 600 GAAGGCTCGG CTCAGTGTCT TCTCTTGGAA GAGAAGAGTG TGCATGCAGA AGGGTGTAGA 660 AAATGCTAGA CGTGTTTCAT CTTCTTGACA AAATGACATT GTAAGATGTG TGTATATGTT 720 TTTAAAAATA TTACATAGGG GCTGAACATG GTGGCCCACT CCTGTAGTCC AGCACAGGGA 780 GGCGGAGGTA GGAAGATTGC TTGAGGTCAG GAGTTCAAGA CCAGCCTGGG CAATGTAGGA 840 AGACTTCATG TCTACAAAAA AAAAAAAAAA AAATTTCATT 880
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