Tag | Content |
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EnhancerAtlas ID | HS073-10049 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr3:8806780-8808950 |
Target genes | |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr3:8807249-8807270 | TGCTGGTTTCACTTTCTTGAT | + | 6.34 | IRF2 | MA0051.1 | chr3:8807248-8807266 | GTGCTGGTTTCACTTTCT | - | 6.03 | MYB | MA0100.3 | chr3:8808717-8808727 | GACAGTTGGT | - | 6.02 | RREB1 | MA0073.1 | chr3:8808381-8808401 | CCCCCCAACACCCCCTTCAA | + | 6.28 | ZNF263 | MA0528.1 | chr3:8807006-8807027 | GGAGGAAAGGGAAGGAGAAAA | + | 6.01 | ZNF263 | MA0528.1 | chr3:8808560-8808581 | CTTACCTCCACCACCTCCTCC | - | 6.11 |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I008766 | chr3 | 8807929 | 8808317 |
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Enhancer Sequence | CTCTGGCCAG GATCTGTGTG TGTCTGTTTT TTCCTCTCTC TTTTGCTTCT AAGACAAAGA 60 AATCAATTGT TGACGTGCTT TTAAAGTGTA GAAAAGATCT AAACTTCGCT TCACGGTACG 120 TGTGACGTGT TGACCACACA CTCTCCTTCT TTAGGGAGGA CACACAGTGA GAAGAGGAGT 180 GCAAGTGAGG GGGCTGAAAA GCAGGAAGCC ATAGAGGAGG GAGCTGGGAG GAAAGGGAAG 240 GAGAAAAATC ACCAGAGACT CAAGACATGA ATGGGAGAGG CGAGGGGACC CCAAGGAGAG 300 AGGAGTGGAA TGTCTGTTGA ATGAATTAAC TGAATGCTGA AATGTCCTCA TTCTAAAAGC 360 AAGACTAAGG CTCAAGGGGA ATAAAGAGAT CTCTCATCTA ACATCCCAAA GCTAGTAAGG 420 GCTGGAGGAG GACTAGACCC CACATCTCTC CAGTATCTAC TCCAAAGGGT GCTGGTTTCA 480 CTTTCTTGAT AGTTGGTGTT CGAGCTCCTC AAGACCTGGA TCTGGTTTCT TCAGATCTGC 540 CCAGGAAACA GGTGAGGCCT AAGGCCTTAC TTAGAGACTT CCACTACTGG CTTTTGCCCA 600 ACCCCACTCC CTCATCATGT GTCCTTCATA AGAACCCTGG CATAGGAAAC GTCAGCTGTG 660 CCTCTGACTT GCTGTGTGAC CTGGTGCAAG TGCCTTCCCC TCTCGGGGCC CTAGAACCCT 720 CTCTGTAAGT TGTTACCAGG GGCCACAGGT GTTCGGTAAA TATTGAATAA CCAGTGTCTT 780 GGCCACTAAA GCAAACACTG AGCTAACTGG GAGGGTTCCA TAAAGCCTGG AGTCTGTGAT 840 TTTCAGAAAG GACCAAAGCA AAGTTACCAA ACTGAATGAA AGCAGCTGGC ACTGAGATTT 900 CGGCTTCCCA GGATGCATGT ATTTGAGACT ATTGGGAGCA GTAGTAACTG CACACAGAAA 960 TGGGACATTT GCAGTGTCTG GAGTGCAGAA AGGGTGAAAG CAAATCCTTT GGTCTTTCTT 1020 TACAAACATT TGAAGTCCCC AGCATCCAGC ACGCGTTATG GGATTGCCTT CAAACAAAAA 1080 CTTATAAATC ATTCACCACC AGCAATCACC CCCTCCTGGT CTTTCCAAAT GAGCTACTGG 1140 AAAGGGGTTG GGGGGCAGGG AGTGACAGGA AGCTGCCTGG TGCTCTGTGC CTTGGGGACA 1200 GCCACCCAGC ACCAGCCACA AACCCCAGAG CCCTAGGGTG CCTCTGTTCC TCCAAGCTTT 1260 CTCCCTAGGT CGCCCTCTTC TATGCCCTCC TCTTAGCTTT CTGGCACAGG CCAAGAATGG 1320 ACAATTGCCC CACCTTCAGC CTTGTCCTCA GCAGTCCTCC TACCTGGAAG GCACATTCCC 1380 CACCTACAGA AATCACCCAG CCTCCCCCTC AAACTTGAAT GTCCCCCTCA AGGCTTTCTT 1440 CTCTTTCCTC CAAGTGGAAG TGAAGTCTCA GTCCTGGGCG CTCTCCTCCC TAAGCCTGCC 1500 CACCACTCCT TGCAGTACTC ACCTCTCTGC ATGGAGACTC ATCACCTCCA CTCGATGAGG 1560 AGTTCAGGGA TTTGTCTTCA CCTCTCCCTT GGACTCCTCT GCCCCCCAAC ACCCCCTTCA 1620 ACTACTAGGT GCTTGGTTGG ACAAATTGCC ACTCCTGCAA GGCTGTCCTT GTCCAAACCA 1680 GACTTCTTGG CTTCAGCTGG ATTTCTTGAA CTTAAAGTGG AAGTTCATCT TAACGTGAAC 1740 TTAAAGTTGA AGGAGCTTGA GCTTGGCCAG GGGTTCCAAA CTTACCTCCA CCACCTCCTC 1800 CTAACCACGT GGGAAAGCAG ATGGAGTCCC TTGAACCTGT TTCCACCACC ACAGTAAACC 1860 ATACAGCCCA TATGCAGCCC AAGGACTGTG CTAAGGACTT TAACTGCATT TTCTCGTGGC 1920 ATTCCCCTAT GCCTGGTGAC AGTTGGTACT TTTATCCTTA TTGCCACCTT ACAGAAGAGA 1980 AAGTGGAGGC TCAGGGAGGT TAATTGCCCT AAGTCACTTG GTCAAGGGAT GACAGAGCAG 2040 TGACTCTGTG GGATTTCAAA CCCGCTTATC CCCCAGGAAG TCCACAGACC CCTGGACATT 2100 CTGAGGCAGC AAGATAAGGG CCTCCCCCAG CCACCAGGCT CCCTCCTCCT GGGTCTCCCA 2160 GCCCTGGCTA 2170
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