Tag | Content |
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EnhancerAtlas ID | HS056-04567 | Organism | Homo sapiens | Tissue/cell | GC_B_cell | Coordinate | chr14:90239390-90241010 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr14:90240866-90240881 | GAGGTCAGGAGTTCA | + | 6.22 |
| | 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 |
GH14I089772 | chr14 | 90239251 | 90240820 |
| Enhancer Sequence | ACTAAGAAGC TCACTCAGAA CTCCTTAGGA AAAAAGAAGA GTACGATGCA GGTGCTTTAG 60 GGTATAAAAT CTCCAAGATC TCTCCATCCT GCTGCTTTGT TCTTGTCATC GTGTGGTTGA 120 AGCTGGGTTG CCTCAGATTT GGGTTCCAGC TGATGGGAAG GGGAAAGAGC ACGTGGAGGG 180 GTATGCAGCT GGCGTCCACA GGTGCAGCTC TGGAGCCGGC ACACCCACTT GCCCAAACAT 240 GCATGTGATA AGTAGCAGTG ATACGGCCAC CCCTAACTGC ATGGGAAGCT GGTTCATGGC 300 TCTGTCTGGG GAGCTGTGTG TGCAGCCACA GCTGTATTTC TGAAAGAAAG ATGCGGATGC 360 ACAGCCAGCA GTCTAAAGCA CACCAGGTGT TTGTGGATTT AAACAATTGC AATAGCACAT 420 CCAATTTCAA CACATGCGAA GTCTGGAGTG AGGTGAAGAA AACACCACTT CACAGGTATA 480 AAGTGCTGGT GAGCAGAGCC CCTCAGGGTC TACTGTGGGG GGCTTGGACT ATGGCAATTT 540 AGTGAACCTG GAACTACATT TTCTAGAGTT CCTTTCCTGT AGGGTTTCAA GTTAGGGCTG 600 ACCAGGAGAG AAATTTGCAT GAGATATGGA AGGTGGAAGT GAAGCAGCAG CTCTCACGCT 660 CCGCAGGTGG GTGCGGGGCA CTGTGCATTG TTACTGTAGC TCCAGTGCGT TGCCACTGAT 720 CTGCTGACTC ACCCGGTGGC GGCTCGGGGC AGCCAGCCCT GCAGTTCCTC AGCAGCTGCC 780 CCATATCCCT CTTTAGCATC GCCAAATCCT CCCAGGTGCA AGTGTTCTTC AATGATGAGG 840 GACAGCAACT CCTGCTTTGG GTTATCCCTT CACTGAGGGG GGCTGCAAGA GGCAGACATG 900 GCTTATAGGT TGTGGCCTTT CTTCACATAA GGGTCTCTCA GCCTCAGCAC TGTTGCTCTT 960 TCAAGCCAGA TAACTGTGGT CAGAGGCTGT CTTGTGCATT GCAGTGTTTA GCAGCATTCC 1020 TGGCCTCTTC TCACTAGATA GTCGTCACTC TCACCTAAGT TGTGGCCACC AAAACTGTCT 1080 CCAGGCATCA ACTCCAAATG TCTTCTGGGG GACAAAGTCG TCCCGGGTTG AGAACCACAG 1140 CCTTCACATC CGGCTTTTTT TCTCAACTGC TGGCTTTGTG ACCTAGGGTA ACCTCAAGCC 1200 CATCTGCAGA TACAGAGGTC TAGCAGCTCT GCTGAGACCT CTCCATCAGC TGCCACAGTC 1260 ACAGAAAAGC CAATCCTTAG ACTCGGTCCC TTATTCCATG TTACTCACAG CAGTTCTGCT 1320 CAGATGAATT ATGACTTCTA TGCGCTGAGC CACTTTGCCT TCATGGACCT TATTCTACTG 1380 TTAAAACATT TTTTAAAAAA TTATAGTTTA GGCCAGCTGT GGTGGCTCAC ACCTGTAATC 1440 CCAGCACTTT GGGGGGCCGA GGTGGGTGGA TCACCTGAGG TCAGGAGTTC AAGACCAGCC 1500 TGGCCAACAT GGAGAAACTC CATCTCTACT AAAAATACAA AAATTAGCCA GGCTTGGTGT 1560 CAGGTGTCTG TAATCCCAGC TACTAGGGAG GCTGAGGCAG GATAATTGCT TGAACCTGGG 1620
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