Tag | Content |
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EnhancerAtlas ID | HS161-14265 |
Organism | Homo sapiens |
Tissue/cell | PC3 |
Coordinate | chr7:100876200-100877550 |
Target genes | Number: 12 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr7:100877123-100877138 | TGAACTCCTGACCTC | - | 6.22 | SP2 | MA0516.2 | chr7:100876540-100876557 | CCAAATCCCGCCCACCC | + | 6.29 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_28156 | chr7:100874742-100876791 | Fetal_Intestine | SE_28156 | chr7:100876976-100884675 | Fetal_Intestine | SE_52423 | chr7:100874627-100885461 | Small_Intestine |
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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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Enhancer Sequence | GACCGGAGGA CGACCCCAGT CCAGTCCAGG GGGAGGGATA GTGGGGGAGG GGGCTTAGGG 60 GAGAGGCAGG CAGGGGCTGC CCAGAGTAGG ACGGGGGCAC CAAGTCCCAG AGCAGCAATT 120 TCACTCAATT CCTTTCTCCC CACCCCAGTT TATAAGCCTT CCTCCTTCCT GGGGTCAACT 180 TCTCAGGGTA GCCCTTAGGC CCCAAGTCCA GCCCACCCAG CTCATCTCAC ACTACCTCAA 240 CCTCCTCCTG CCTCTTCTCT CTTTGGTCCC AGATCTACCT AGTTCATGCC CACCTCTAGG 300 GCCTTCATCC CATCATCTCC TCACCCAGAT GGAGCCCCAT CCAAATCCCG CCCACCCTTG 360 AAACCTTGAA AACCCAGCTG GGCCATGGGA GTCCAGGGTC GTCCTTTCCT GAAGCCAGGC 420 AGACCCCCGG GCTAGCACCA CCCTACTCAC TGGGGGCTTG TCCTCTTGCA AGCCACCTGA 480 CCTTTCTGGG CCTGTTTTAC CTCTGGAAAA CAAGCAATAC CCACCCTACC TCAAAGGCTT 540 ATTGTGAGGC AATGGGTACA GAAATGTTCT GCAAATTGAA AAGCAATGGC CAGATGGCAT 600 TGTTTTTGTT TTTTGCTGAG ACGGGTTCTC ACTATGCTGC CCAGGCTAGT CTGGAACTCC 660 TGGGCTCAAG GCAGTTCTCC TGCCTTGGCC ATTTTTTTTT TGACAGTCTC ACTCTTTCAC 720 CCAGGCTGGA ATGCAGTGGC ACAATCTTGG CTTACTACAA CTTCTGCCTC CCAGGTTCAG 780 GTGATTCTCC TGCCTCAGCC TCCAAGTCAG TGGGACTACA GGTGCCTGCC ACCACGCCTG 840 GCTAATTTTT TTTTTTTTTT TTTTTTTTTT TTTTTGGTAT TTTTAGTAGA GACAGGGTTT 900 CACCATGTTG GCCAGGCTGG TTTTGAACTC CTGACCTCAA GTAATCCACC CACCTCAGCC 960 TACCAAAGTG CTGGGATTAC AGGCATGAGC CACCATGCCC CGTGGTATGG CACTGTGGAC 1020 GTGCACTGTG TGTGTGCGCC ATAGCGTGCA CCCTAACTCT GCTCCCCAGC TAGGATGTAA 1080 GCTCCCGGAG GCAGCCGCTC ACTCTTATCT TCGAAGTCCC TCCCACACCT GGCCGTGGCC 1140 AGCCCCTACT GGGAGCTCAA GAAACACTGC CGATGGGCTG ATTTGCAGCC AGGAGATCTG 1200 GGGAGTACAG ATGAGGCAGG GGTGAGCAGG TGTCCATGCA GCAGGGTAGG GGAGGTGAGC 1260 ATGAGGAGTG GGAATTGGAG AGGAGATTAG ATGAGGACAA AGCAGCCTGA AGTCTGCGGT 1320 TGAGGGGGAC CCCCGCCCCA TCACCTTCCC 1350
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