Tag | Content |
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EnhancerAtlas ID | HS184-19111 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr21:45789800-45791220 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUN(var.2) | MA0489.1 | chr21:45790325-45790339 | AGATAATGAGTCAT | + | 6.03 | KLF14 | MA0740.1 | chr21:45790074-45790088 | GAGGGGGCGTGGCC | - | 7.52 | KLF16 | MA0741.1 | chr21:45790076-45790087 | GGGGGCGTGGC | - | 6.62 | SP1 | MA0079.4 | chr21:45790075-45790090 | AGGGGGCGTGGCCAG | - | 7.26 | SP3 | MA0746.2 | chr21:45790075-45790088 | AGGGGGCGTGGCC | - | 6.82 | SP4 | MA0685.1 | chr21:45790073-45790090 | GGAGGGGGCGTGGCCAG | - | 8 | SP8 | MA0747.1 | chr21:45790075-45790087 | AGGGGGCGTGGC | - | 6.92 |
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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 |
GH21I044368 | chr21 | 45788471 | 45791547 |
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Enhancer Sequence | GGGTGAGTTC TGACCGGGTG CTGCGGGGAG CAGGTGGAGT GTGCGGGGGA GGCGGGGTGT 60 GGGTGACGTC TGACCGGGTG CTGTGAGGAG CAGGTGGAGT GTGCGGGGGA GGCGGGCACA 120 CTCAGGAGAT TGGGTGCAAC TCCCGGCCCA CCCCTGACCC AGGTGACCCC GGACAAACGG 180 CTAACTTGGC TGGACTCTGG TATCTCCCTC AAGGTTGTAA GAGGGGTCCA CGTGACAGTC 240 ACTCGCTGCG AGGGTTCCGC TAACAGAGCA GAGGGAGGGG GCGTGGCCAG CAGGCAGCTG 300 GGTGGGGCTG AGCCAGGGCG ATCCGACCCC GAACCGGAGC TTTTAGCACT TTGAGTCCCT 360 GTACTCAGAG GTCTCCTGCA GCCGGGAATC CCACTGTGCT GTGGTCCCTG GCAGCCAGCA 420 CCCACCCCCA GCTTCTCCGT CAAGGTTGAG GACGGAGCAC TCCTGCCTCT GATTAACTGG 480 ACGCAGGAGA AGCAGTTGCT TTAATCCGGA GCCTTGAGTT GGGACAGATA ATGAGTCATT 540 CAACCAGATT TTCCAAGGAC ACACTAACTT TGGTATGATG CGTGTGTGCC CCTGAATCCA 600 CGTGGTCAGG AAAGCCCAGG GAACACTGGC CTGTGACTCA CTGAGCAGGT TCCCTTGTTA 660 CCCCGAGGGG TGATTTACTC CTCTGACAGT GACACGGACA CTGTGCGTCC ATTCCCCGGG 720 CGGGCAGAGG ACACTCCCAG ATGCCCACGA GGGGCCCAGC AAGCACTGGC CAGCCCCAGC 780 CCGGCCTTCG CCTTCCTTTG CGTCAGAATC ATGAATGTGT CCGGCGGGGT CGGACTGGAC 840 CAGCTGTTGG GCTTTGTTTG CTCTTTTTAC GAATTGAAAA ACTGAAGCCA GGAGCGGCTG 900 GGTGACGTCC CAGGTCACTC CTTACTTTCC TCCCCACGCT GAGCTCAGAC GACTTCCCGT 960 GACACCACTG TTGGTGGCGG AATGGGACTG TGGCTGCTTC CGCTCAGCCA CGCTCCCTCT 1020 CTGTGGACGG CGGAGGGTGT GTGTCCCAGC CCGGCTGCCG CCCTCCCTTA GGTCTGTCTC 1080 CCGGGGCTGC TGTAACCCAG GCTCACAAAC CTGGTGGCTT AAAGCAGCAG AAACTTAGTC 1140 TATCAGATCT GGAATCCGCG TCGATTGGCC ATCATCCAGC CATCGGTGTT GGCGGGGCCA 1200 CCTCCCTCTA GGGCCTAGGG GAAGAGCATT CCTTGCTGCC TCCAGCGTCT GGGTGCTGAT 1260 GGCATTCCCT GGCCAGTGGC CACCTCCCTC CAGTCGCTGC CTCCGTGTCC CATGGCCGCC 1320 TCCCTCCAGT CTCTGCCTCC GTGTCCCGTG GCCGCCTCCC TCCAGTGTCT GCCTCCGTGT 1380 CCCGTGGCCG CCTCCCTCCA GTGTCTGCCT CCGTGTCCCG 1420
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