Tag | Content |
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EnhancerAtlas ID | HS150-03316 |
Organism | Homo sapiens |
Tissue/cell | NT2-D1 |
Coordinate | chr12:115889900-115891200 |
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) |
INSM1 | MA0155.1 | chr12:115890854-115890866 | TGCCTGGGGGCA | + | 6.04 | ZNF263 | MA0528.1 | chr12:115890054-115890075 | CCCTTCCTCTCCCTCTCCCTC | - | 6.3 | ZNF263 | MA0528.1 | chr12:115890022-115890043 | TCCCCTCCCCTCCCCTCCCCT | - | 6.91 | ZNF263 | MA0528.1 | chr12:115890027-115890048 | TCCCCTCCCCTCCCCTCCCCT | - | 6.91 | ZNF263 | MA0528.1 | chr12:115890032-115890053 | TCCCCTCCCCTCCCCTCCCCT | - | 6.91 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I115451 | chr12 | 115889005 | 115891497 |
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Enhancer Sequence | CCGCCTCCTC GAGCCCAAGG CCGCCGCGCG CCGCGCTCGC CGCTGATAAG AGGCGGCGGG 60 GGAGGGGCGC AGGATGCTGG CGTTGCGGAA GGGCGGGGGA TGGGTGGGCA GCTGGAGCGG 120 GCTCCCCTCC CCTCCCCTCC CCTCCCCTCC CCTGCCCTTC CTCTCCCTCT CCCTCTGCGA 180 TGTCTCTCCC GAAAGTGTGT GACTTGCCCA TGTCTGTCTC TTGTCTGCGC CTCTCCCCTA 240 AATTCCCTCC CTCCCCAGCC CTCGCCGCGA GCGTGTGTGC GCGCGTGTTC GTGTGTGTGT 300 GCGTGTGCAT GTGTGTCTGT GTCTCCAGTT GCTCCCTGTC TCCTGTACCT GTCTCTGTGC 360 ACTTCCTGAC CTTTCTGTCT CCTACTCCCC ACCTCTCTGA TTCTCTCCAC CTCCTGCTGA 420 TTCTGTCGCT CTCTTCTCTC TTAGCATCCC CTCTTAGTTT CTCCCTCTCT CCCTGTTCTA 480 TTTCTCTCTT CCTCACCTAA CTTGGAGCCA GTCCCTCCCC TCTCCCTGTG TCTGTCTTCT 540 CTCCCTCTCT CCATCTTTCT GACTCTGACC TGCCTCTCCC CTTCTCTCTC CCTTCCCTGT 600 CTCTCCGAGT CCTTGCCTGT CCTCCTCTCT CTGCATCTTT TCTTTCTGCG TCCCCAACTC 660 CCTCTCACTT CTCCGTTCTT TCACTCATTT GTCTGTATCT TCCCTTTTCT TTTCTCGCCC 720 TGGGCTCCTC CCCATAACTC TGCGTGTCCC CTGCCCATCT CAGCATCCTG TGGCACTTTC 780 TGCATGGCCG GCCCGCCTGC AGGGACAAGG CCTTCAGAGC CAGCGGTTGC AGGAATAGCT 840 GGACCCCACA AGGGGCTAGG CTCAGCAGGT GTCCTGACTT CAGGGGGCAG GACTGTGCTC 900 ACCTGTGCCT TTCATGTAAG GCTCTGGCGC ACTTCACAAA CAGTCATTAA GGCCTGCCTG 960 GGGGCAGGTC AGGGAATATC ACAGCCTGGG CTGTTTGGTT ATCTTCATTA TTAATACACA 1020 CTCCCCTGCC TTAAATGAGT TTAGTGCAGG GGACAGAATC CCGACTGACG CCTGGAGAGA 1080 TTAAGGTTTC CGAGGGTTGC ACAGGCCAAA GATGACAAAC TGATACAGCA GGGATGTGAG 1140 TTTCTGCTGC TTCCTTCCTG CAGTGCAAGC CTCTGCCAGG AGCTTATAAA CCACCCTTTC 1200 TGAGACGGCT CTGGGGGTCA AGAGATGGGG CTAGATTTAT CTGAATGGGT CCTGGCCTGG 1260 TGGTCTGCTT TGCACCAAAC ATGCAAGCAG GGATCTCAGT 1300
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