Tag | Content |
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EnhancerAtlas ID | HS007-07874 | Organism | Homo sapiens | Tissue/cell | BE2C | Coordinate | chr19:1331000-1332300 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr19:1331271-1331286 | TGGGTCAAGAGGTCA | + | 6.57 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TGGGCAGATC ACCTGAGGTC AGGAGTTCGG GACCAGCCTG ACCAACATGG AAAAACCCCG 60 TCTCTACTAA AAATACAAAA TTGGCCGGGT GCGGTGGCTC ACACCTGTAA TCCCAGCACT 120 TTGGGAGGCT GAGGTGGGCG GATCACGAGG TCAGGAGTTC GAGACCATCC TCGCCAACAT 180 GGTGAAACCC TGTCTCTACA AAAAATACAA AAAATGGCTG GGCGCAGTGG CTCACACCTG 240 TAACCCCAGC ACTTTGGGAG GCCGAGGCAG GTGGGTCAAG AGGTCAGGAG ATCGAGACCA 300 TCCTGGCTAA CACGGTGAAA CCCTGTCTCT ACTAAAAATA CAAAAAATTA GCCGGGCGTG 360 GTGGTGGGCA GCTGTAGTCC CAGCTACTCG GGAGCCTGAG GCAGGAGAAT GGCGTGAACC 420 TGGGAGGCGG AGCTTACAGT GAGCTGAGAT AGCGCCACTG CACTCCAGCC TGGGCGACAG 480 AGCGACTCCA TCTCAAAAAA ACAAAAAAAA ACAAAAAAAA ACAGCTGTGT GGATTCCTCC 540 GGGGCACGCT GGGCCTCCGG AGTCTGGAGT GGGGGCTAGG GGCTGCCTGG GGAGGGGCTG 600 GAAGGGAAGC AGCAGACAAT GGGCTGGGCT GCACCCCTCC CCCGGTTCCA GTTCCCCCCA 660 AATCAGACGG ACACGGCTGC AGAAAGCTGC GGCCTCTCAC GCGGCCAGGC GCGGGGCGCA 720 CAATGCTTGC TGTCGTCCCG TGTTTTCTGC TGTCCCCGCC TCCGTTGTCT GGGTCCCCTG 780 GGGCAGCTGT GGAAATTGGG GGTTGAGAGC CCTTCCAGGC AGGCTATCTT TGTGGCTGTT 840 TCAAGCATCC TTTGGGAGAC AGTAGGGGAC ACCTTCCCTT CCGCCCTCTG GACGAGGCAG 900 GGGTGACAGC GTCGGTGCGT GTACTGGGCT CTCGGGAAGG AGGAGGGGGC CCGGCTCCTG 960 GTCCCTTGTC CCTTGTCCCT GCTCAGTCCT GGTTGCAGGC ATTGTGGGCA CCACCCGTGC 1020 TGCCCACAGG AAGATCATTG TCCGTAGCAG CATCCTGAGC TGTGACCTGC GTTTATTTCC 1080 CCATGGGGAC GTGGGGTCTC CCTGATGTCA AGAGAGGCGG TGTCACACAG GCATTTAACA 1140 TGCCACTGCC ATGATTGGGA CTGGGATTGG GACCAGCACA GCCCCTTGGG GGATGTGGCG 1200 GTGTGGTGGG AGAGGGGCTT GGGAACCCAC CAGCAGCCTA GCCCTGGAAG CTGCGTGTTG 1260 TAGATTATGG AAAATGCTGC AGCACTCAGA ACGAGACATC 1300
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