Tag | Content |
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EnhancerAtlas ID | HS091-05527 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr10:71875520-71876370 |
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) |
CTCF | MA0139.1 | chr10:71876131-71876150 | TTACCACTAGGGGGCGGCC | + | 7.7 |
|
| Number: 2 | ID | Chromosome | Start | End |
GH10I070116 | chr10 | 71876041 | 71876230 | GH10I070117 | chr10 | 71876241 | 71876430 |
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Enhancer Sequence | CAAAAAATAA AAATAAAAAA CAAAACTGAA GCATTAAAAA TAAATGCAGA GCTTTAATAA 60 ATGGCAAACT GCTTTTTTAA AGGGACTTTT AAAAACTTGT ATTTGAAAAT ACAACATTAG 120 GACAATTTGG TATTAAATTC TGGGATCTCT GTCCATTATA AGCCCTCAAT CCCACTGCTA 180 CACACAGCCT GGACTGGCTT CCTTTTCCTG GGATTGGATC ATTACTTCCT GCTGGACACA 240 AGGCAGGAGC TCCTTGTCAG GGAAGGGCAT TTGGGAGTAA ATGACAGGGA ATTGAGGACA 300 CAAAGCAACC ACCAGGCCTG GCCACTGAGT CTCCTGCTCA CAAATGGAGG CTTAAACACA 360 CATCAGTCCA CCTCTGCCAC CTCCAGCCAG CTAAATACGC AAATACTGAG CTTTAAGAAA 420 CGAGGCCATG TTACCAACCC CACTCCCCAG TCAATCCAAG CTCAAGAGAC CAAATGTTTT 480 GATCTGGGTT TGGGGGCGGC AGCACGCCTG CCAAGAGAGG AAGGCCTGAC CCTGAATTTC 540 CTCTGTCCTC AGGTGAGGGG GAAAGAAACA CCACCAACCT TTGTCATCTC TCTGACGCCT 600 GTTCCCATCT CTTACCACTA GGGGGCGGCC CTAATTTCAG AAGATTCTGG TCACCTTGGC 660 CACCTGGGGC CGAGCCATGG TCACAGCTGA GGAGAGCTCA GCAAGGGTGG ACCCTCACTG 720 AATTTAAAGT CTGAGCTGTT GGGAAGAAAG GGGGAAGGCA GCAAGGTGTG GACTCCTGGG 780 GGCAAGCACT GCAGGGCATT CAGAGGGTAC TGGAGAGCAA GGAGGCACAG GGGAAGCCCG 840 GCTGGGCACC 850
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