Tag | Content |
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EnhancerAtlas ID | HS078-09089 |
Organism | Homo sapiens |
Tissue/cell | H2171 |
Coordinate | chr19:51360420-51361280 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr19:51360605-51360626 | GAGGAAGGAGAAGGGGGAAGG | + | 6.46 | ZNF263 | MA0528.1 | chr19:51360604-51360625 | GGAGGAAGGAGAAGGGGGAAG | + | 7.08 | ZNF263 | MA0528.1 | chr19:51360608-51360629 | GAAGGAGAAGGGGGAAGGAAA | + | 7.28 | ZNF263 | MA0528.1 | chr19:51360598-51360619 | GAGGGAGGAGGAAGGAGAAGG | + | 7.51 | ZNF263 | MA0528.1 | chr19:51360601-51360622 | GGAGGAGGAAGGAGAAGGGGG | + | 9.36 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_33581 | chr19:51360333-51363639 | H2171 | SE_41577 | chr19:51360446-51363976 | LNCaP |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I050857 | chr19 | 51360334 | 51363976 |
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Enhancer Sequence | AAAAAAAAAA AAAAAAAAAG AAAAGAAAAG AAAAGAAAAG GAAGTGTTTT ATCCCTGATG 60 TGTGTGGGTA TGAGGGTATG AGAGGGCCCC TCTCACTCCA TTCCTTCTCC AGGACATCCC 120 TCCACTCTTG GGAGACACAG AGAAGGGCTG GTTCCAGCTG GAGCTGGGAG GGGCAATTGA 180 GGGAGGAGGA AGGAGAAGGG GGAAGGAAAA CAGGGTATGG GGGAAAGGAC CCTGGGGAGC 240 GAAGTGGAGG ATACAACCTT GGGCCTGCAG GCCAGGCTAC CTACCCACTT GGAAACCCAC 300 GCCAAAGCCG CATCTACAGC TGAGCCACTC TGAGGCCTCC CCTCCCCAGC GGTCCCCACT 360 CAGCTCCAAA GTCTCTCTCC CTTTTCTCTC CCACACTCTA TCATCCCCCG GATTCCTCTC 420 TACTTGGTTC TCATTCTTCC TTTGACTTCC TGCTTCCCTT TCTCATTCAT CTGTTTCTCA 480 CTTTCTGCCT GGTTTTGTTC TTCTCTCTCT CTTTCTCTGG CCCATGTCTG TTTCTCTATG 540 TTTCTGTCTT TTCTTTCTCA TCCTGTGTAT TTTCGGCTCA CCTTGTTTGT CACTGTTCTC 600 CCCTCTGCCC TTTCATTCTC TCTGTCCTTT TACCCTCTTC CTTTTTCCCT TGGTTTCTCT 660 CAGTTTCTGT ATCTGCCCTT CACCCTCTCA CACTGCTGTT TCCCAACTCG TTGTCTGTAT 720 TTTTGGCCTG AACTGTGTCT TCCCCAACCC TGTGTTTTTC TCACTGTTTC TTTTTCTCTT 780 TTGGAGCCTC CTCCTTGCTC CTCTGTCCCT TCTCTCTTTC CTTATCATCC TCGCTCCTCA 840 TTCCTGCGTC TGCTTCCTCC 860
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