Tag | Content |
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EnhancerAtlas ID | HS177-00927 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH_RA |
Coordinate | chr1:84158130-84159840 |
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) |
PRDM1 | MA0508.2 | chr1:84158790-84158800 | TCACTTTCAC | + | 6.02 | ZNF263 | MA0528.1 | chr1:84158327-84158348 | GGGGAAGGAAAAGGGGAGGGA | + | 6.26 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I083692 | chr1 | 84157716 | 84160777 |
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Enhancer Sequence | AACCCAGTAG CCTGCCAGTA ATCATAGGGT CCAAACATAA ATGTTACCCT AACCCAAATG 60 GCCACGGATC TTTCCATCAC CATTAGTCAA CCTAATGGAT CTGCTGACTT CAGTCCCACA 120 GAGAACGGCC ACTGACTTCA CAGCAGGCAG ACCCATGGAG AGCAAGGGTC AGCCAGCTAC 180 TGAGCATTTA AAACAGTGGG GAAGGAAAAG GGGAGGGAAA TGCCTCTCAG ATAAATCACC 240 GGAGCTGTCT GGGGTGAGCA GTGCCCGTGG TAAGTGAGCT CCTGCAAGTT CCTGTCACAG 300 ACCTGTCCCT TCCACCTCCT ACCCTTAAGG CAGTTCCTGC AGCTCTCACA GCTGTGCCCA 360 CACTTTCACT CCTGCAAAGA ACGTCTCATT GGCTTCAATT GCTTTAGCGG CTCAGCGTGG 420 TCCCTGTCGG GAGCACTTGT CACCTCCTTC CCAAGCAGCC CGCTTGACAC CCAACCTAAT 480 TCCTACTTGG TGAACCAAGC CCCCAAGGTT CCTTTCACCC CCACCCCTGC CCCCCATTTT 540 GTGAAGAGCC AAATTCAGCA GCTCCAATCT CAGCTTTATT TTCATGCAAA GTGAAAGAGC 600 TCAGCCACCC GGCACTGGCT GAAGGGTAGA TAAAAGCCCC AGCTGTGCCT GCTCTGGGAG 660 TCACTTTCAC CTCCAGCAGG AAAGCAAACT GTTTTTGTGC CTGAGGGAAA TTATGGAGCC 720 TCACACTTTC ATCCAGAGAC GGACAAAGGG GAGGTCAGGT GCTGCATCTG CCAGAAATGG 780 GGACGTGTGA AATGTGATTA ACCCAAGGAG AAGCCACACA GAGCCCGGCT GGGGCCTCTC 840 CTGTCCCTGT GTGTTTCCCA GTGTCAGAAG CAGGCAGAAG AGTAAACAAA AGCATTAAAT 900 AAATATTTTT CCGTTTAACC CATGTGTTAA TACAGATTTT TACAACCTCG ACAGCACTGA 960 CTGAATCAAT AGTTGCAAGT ATTAGCCTGA ATAATGAAGG AAGTAGTGTA CATCTGTTGA 1020 TTTCTCTGCA TTTGTGAAAA GAAGGGGGGT GGGGGGGTGA GGAGGGGAAG AGATTCCAGA 1080 ATGAGCGTGT AATCACATTG TACCCTGCCT GTCCGCAGCA CAGCTAAGCC TATCGGGCCC 1140 ATCAGATGAA CTCGCTAATG CTATTTCTCA GGCTAAATAC AAACCGCTGG TGCCTGTAGA 1200 ATTAAACTCA TCAATAGCTA AGCTCTCCTG CATTTACAGG AAGACACAAA TAAAATTCCT 1260 ACTGATATGC CCATCAGAGT GGGAAGTTAT CTGTCTCTTT CGAACAGACT TTCTGTAAGA 1320 GCTCTGTGTG GTAAATGAAG CTACCAGTAC ATTTGTCTCT TTGTCAAAAT AAATAATGCC 1380 AATTTCATTT TTGAACAGTG TGCTTGGGCT GTATTCATTA TTGTGTTAGG GTTTTGTTTC 1440 CGCCAAAACA GCCCTCCCCA GCCCTGCTGC TTGGACAACT TGTCTCTGAT TAGGGATGTG 1500 TGCTGAAAAC GGAAACTGTT TGAAATTAAC TAGAGACGTA TTAAATAATC ACAAAAGAAA 1560 TTCCGGTAAA AAATAGAGTC AGTTATCAAA AGATTAACAC GGTTCTTTGT TCCGTTTTTT 1620 TTTTTTTTTT TAGACAGGGA GGGGAAGCAA TTTTCAAGAC AGACACCAAT GCTTTAAAAG 1680 GATTTTTCAG AGGTGAATTA CTTAATCCTT 1710
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