Tag | Content |
---|
EnhancerAtlas ID | HS069-08096 | Organism | Homo sapiens | Tissue/cell | GM18951 | Coordinate | chr8:38384390-38385840 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUND(var.2) | MA0492.1 | chr8:38385237-38385252 | AGAAGTGATGTCATC | + | 6.16 | TCF7L2 | MA0523.1 | chr8:38384684-38384698 | TCCCTTTGAAGTTC | - | 6.4 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGGCCCAAAT GTAAGACCAC TCCACTCCAG ATCTAGTCTG GAGCAGTGAT TTCTCTGCCC 60 CTCCCATTCT CCTTGCCTCA TGTGCCCTGA GCACCTCAGC CGCCTCCATG GTCAGTGACA 120 AGCTGTAATT GGAGTGAAAG GGCTTTGAAG TTCTGATAAA TGAGATAATA AATCTCTGCT 180 CTCCAGGGAT GTAGGGCAGT GTCTGTGCCT ATTGAATGGC CTCAACAGTG CTGTGTATAT 240 AGTAACTACT TAATTATTAT GAAATAATTA TTATGAAATA AGTGGTTGAA GTGATCCCTT 300 TGAAGTTCAG GTCAACTCTG AGCCATCTGA GAAGAATGAA TGGAATGGGT AATTGAAACA 360 GATAATCCCC AAACCTCAAC TTACTAGTTA ATAGGGTTAG GCTCTTTACC TATTAAACCC 420 TTTGAGATAC TCAATTTGAA AACTGCTAAA ATAAATCCCC TACTTTCATT TATTTTTTCA 480 TTGTTGTGGG GCAGGAGAAA TTGAGCTGTG AAATGGCCAC CAGGAAGGTG GCAGGATGAC 540 GAGTCAGGAG TCCTGTGTGA GACATCCGCA AACATCTCAT AAGCAGCTTC TGAATCACAC 600 AGCATCAAGG CTGCCAAAGT GCCTGGCCAA TCTTGGACCT AGAGACCTAA GAATGGGTCT 660 CCCTGTGGAC TCCTCCTGAC CTGGGTGGGG CAAGGCTCTT GGAAAATAGG TCAAATGACT 720 CTCAGTCTAG AACCGTCTGG CCAGAGATGC CCCAACTTTG CCTTTTGGGC TATTCATCAA 780 ATCCAGCCTT TAGGACGTGA CATCAGGGTT TCATTTCATG GGAAGATCTG GGTGCATTTT 840 AGTTAAAAGA AGTGATGTCA TCACATCCCT GCTGAAAAAA GGAAAAAGGA CCCACTTTGT 900 GCTGACATAC CGAGTCCTGG GCAGGGAAGT CTGGACAGAC ACCTGGGTCC ACACCTGGCT 960 TTTCTACCAG CTAGCTCTGT GACTCTGGGA CCATTGTGTC AGCTTTCTCT GCCACAGTTC 1020 CTCCCTCTGC AAAACGAAGG GCTTGAAATG CAGGATTCTA AGATTGTGGC CATCTCTGAC 1080 TCTGATAACA ACCCCGTGAG CCTGAAGAAT TCAGCACTGC TGCTCCATAG GGGGTTTCAG 1140 CAGGAAGCGG GCACAGATGG CTTTCTCTGG AACGTGTTCA GAAATGTGGT GTGTGATGTA 1200 CGGTGTGAAT GAAGCGTGGT GCCCTTTAAA CACAGCTTCC CCCTGGGAGT GCTCTGAGCT 1260 CCTCGGGTTC TCTGGCTCTC ATTCACATTC CACTGTCACT CTGGGCACTG GCAGCCCTCA 1320 CGTGCTTGTG CACTGAGCAC ACACACACCC CGCCCTGACT GACACACAAT TGGTGACTCA 1380 CAACTGACAC AATCATTACA CACATGGAAT GACTCAGCGG GGACACTCAC ATGCATGGGC 1440 TCACGCTCAC 1450
|
| |
|
|
|