Tag | Content |
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EnhancerAtlas ID | HS196-10936 |
Organism | Homo sapiens |
Tissue/cell | ZR75-1 |
Coordinate | chr16:30867670-30868860 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr16:30868493-30868508 | GAGGTCAGGAGTTCA | + | 6.22 | RARA(var.2) | MA0730.1 | chr16:30868110-30868127 | AGGTCAGCTAGAGGTGA | + | 6.18 | Stat6 | MA0520.1 | chr16:30868784-30868799 | ACTTCTCTGGAAACA | - | 6.12 | Zfx | MA0146.2 | chr16:30868469-30868483 | GAGGCCGAGGCGGG | - | 6.01 |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH16I030856 | chr16 | 30867832 | 30869201 |
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Enhancer Sequence | AGAATCACTT GAACCCAGGA GGCAGAAGTT GCAGTGAGTC AAGATCACAC CACTCTACTC 60 CAGTCTGGGC GACACAGTGA GACTCCGTCT AAAAAAAAAA AAAAAAAAAA AGTGTGGCAG 120 CTCTGAAAAT TAGATTCCCC TCCTCCCTAG GCTTTGTTAT TGTCACTGTA CGTTGTTGCT 180 GCTATTTGTT ATGTGAATCC CTAGACTAAT TCAGTCGCAT CTGTATTCTA CGTTGTGCAG 240 CCACTGAAGT CTGCTCTGTT AGAGCAGTTA GCCCAGTTAG CTTAGTTGTC AGCTAATGAT 300 TGGACAGAGA TTTTCTTAAA TGCCTTTCAC AAATGACTCC CAGCTTTTCC GAGGGGCTCT 360 ATGTGTGTGT CTCAGTGTTC CAAAGACAGT GTATAGCACT GCTCTAACCT TCCCTTGCTG 420 CCGGCCGGCA CAGAGCCACA AGGTCAGCTA GAGGTGAGAG CGTAGGGACT TCTCAGGTCT 480 TTTCTCTGTA TGTTCACAGC CCTAGACATG CTGGTGACCT AGGAATTCCT AAGAATATGT 540 CAGAGCTTTG CTCTCTATTG GATATGGCAT GGTTTTCTTT CCTTTTAAGT TTTTTTGTCA 600 GCCTCTTATA TCTCCAACTG GTATTACCAC CCCAGGCACT TGTGATGTTA AACAGTTGTC 660 ACTGCCTGTT TTTGTTTGTT TTCAACAAAT GCCCTAGGGA CATGGCTGTT AGTAAAGGAA 720 AAGTCCTGAG TCAGGTCAAA TAAAGATAAA CCCTGAGGGC TGGGCACGGT GGCTTATGCC 780 TGTAATCCCA GCACTTTGGG AGGCCGAGGC GGGCAGATCA CATGAGGTCA GGAGTTCAAG 840 ACCAGCCTGG CCAACATGGT GAAACCCCAC CTGTATTAAA AATACAAAAT TAGCTAGGCA 900 CGGTGGTGCA TGCCTGTAGT CCCAGCTACC CGGGAGGCTG AGGCAGGAGA ATCACTAGAA 960 CTCAGGAGGC AGAGGCTGCA GTGAGCCAAG ATTGTGCCAC TGTACTCCAG CCTGGGTGAC 1020 AGAGCGAGAC TCCATCTCAA AAAAAAAAAA AAAAAAAAGA TAAACCCTGA GAATAGAGCT 1080 TTTCAAGGAG TCAGCGGATA GGTCAAATAA TGACACTTCT CTGGAAACAG AGCTTTTGTT 1140 GAGGTTCAAA CCTGTTCTGC CCCTCTAATG GCTGCTAGGC TATTGGTTCT 1190
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