Tag | Content |
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EnhancerAtlas ID | HS086-08839 |
Organism | Homo sapiens |
Tissue/cell | HEK293 |
Coordinate | chr21:45789740-45791160 |
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 | GTGGGTGACG TCTGACCGGG TGCTGCGGGG AGCAGGTGGA GTGTGCGGGG GCCGGGGTGT 60 GGGTGAGTTC TGACCGGGTG CTGCGGGGAG CAGGTGGAGT GTGCGGGGGA GGCGGGGTGT 120 GGGTGACGTC TGACCGGGTG CTGTGAGGAG CAGGTGGAGT GTGCGGGGGA GGCGGGCACA 180 CTCAGGAGAT TGGGTGCAAC TCCCGGCCCA CCCCTGACCC AGGTGACCCC GGACAAACGG 240 CTAACTTGGC TGGACTCTGG TATCTCCCTC AAGGTTGTAA GAGGGGTCCA CGTGACAGTC 300 ACTCGCTGCG AGGGTTCCGC TAACAGAGCA GAGGGAGGGG GCGTGGCCAG CAGGCAGCTG 360 GGTGGGGCTG AGCCAGGGCG ATCCGACCCC GAACCGGAGC TTTTAGCACT TTGAGTCCCT 420 GTACTCAGAG GTCTCCTGCA GCCGGGAATC CCACTGTGCT GTGGTCCCTG GCAGCCAGCA 480 CCCACCCCCA GCTTCTCCGT CAAGGTTGAG GACGGAGCAC TCCTGCCTCT GATTAACTGG 540 ACGCAGGAGA AGCAGTTGCT TTAATCCGGA GCCTTGAGTT GGGACAGATA ATGAGTCATT 600 CAACCAGATT TTCCAAGGAC ACACTAACTT TGGTATGATG CGTGTGTGCC CCTGAATCCA 660 CGTGGTCAGG AAAGCCCAGG GAACACTGGC CTGTGACTCA CTGAGCAGGT TCCCTTGTTA 720 CCCCGAGGGG TGATTTACTC CTCTGACAGT GACACGGACA CTGTGCGTCC ATTCCCCGGG 780 CGGGCAGAGG ACACTCCCAG ATGCCCACGA GGGGCCCAGC AAGCACTGGC CAGCCCCAGC 840 CCGGCCTTCG CCTTCCTTTG CGTCAGAATC ATGAATGTGT CCGGCGGGGT CGGACTGGAC 900 CAGCTGTTGG GCTTTGTTTG CTCTTTTTAC GAATTGAAAA ACTGAAGCCA GGAGCGGCTG 960 GGTGACGTCC CAGGTCACTC CTTACTTTCC TCCCCACGCT GAGCTCAGAC GACTTCCCGT 1020 GACACCACTG TTGGTGGCGG AATGGGACTG TGGCTGCTTC CGCTCAGCCA CGCTCCCTCT 1080 CTGTGGACGG CGGAGGGTGT GTGTCCCAGC CCGGCTGCCG CCCTCCCTTA GGTCTGTCTC 1140 CCGGGGCTGC TGTAACCCAG GCTCACAAAC CTGGTGGCTT AAAGCAGCAG AAACTTAGTC 1200 TATCAGATCT GGAATCCGCG TCGATTGGCC ATCATCCAGC CATCGGTGTT GGCGGGGCCA 1260 CCTCCCTCTA GGGCCTAGGG GAAGAGCATT CCTTGCTGCC TCCAGCGTCT GGGTGCTGAT 1320 GGCATTCCCT GGCCAGTGGC CACCTCCCTC CAGTCGCTGC CTCCGTGTCC CATGGCCGCC 1380 TCCCTCCAGT CTCTGCCTCC GTGTCCCGTG GCCGCCTCCC 1420
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