Tag | Content |
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EnhancerAtlas ID | HS109-15380 |
Organism | Homo sapiens |
Tissue/cell | Kasumi-1 |
Coordinate | chr3:50174990-50176430 |
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) |
RREB1 | MA0073.1 | chr3:50175615-50175635 | GCGCAGGGGGTGGGTTGTGG | - | 6.99 | ZNF263 | MA0528.1 | chr3:50176253-50176274 | GGGGGAGGGGGAGACAGGGAA | + | 6.57 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_63300 | chr3:50160785-50185395 | NCI-H82 | SE_68724 | chr3:50174147-50178900 | H9 |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I050138 | chr3 | 50175637 | 50177745 |
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Enhancer Sequence | CTTTGCTTCC CTTCAGAGAC TCTTCCCACG GCCCTGCATT CCCCACCACC ACACCGGCTG 60 AGCCGAGCTG TCTTTCCCAG TGTCCCAGTG CCCACCCCCA CCCCTATGGC AAGGACAGGC 120 TCTCACACCA GGGGTGCACC ATAAGCATCG TCACCCCTGG CCATGACTCT CCAGGACAGG 180 TGCTCTCAGG GATGATGCCT GACCACCTGG GACCAGCTGT GCTCCCTCCT GCTCCTCCAG 240 CCCTGGCTCC AGTCCCCTTG GCTTTACCAG GCTCTGAAGG CCTGACCTAG ACTCAGGCGC 300 CCATCTGAGG CCCACACAGC CCAGCTGTGC CTGCCCTCGC CCACCTGGAG AAAGAAGGGG 360 CTGGCATATC TTCTTTCCCC ACTCCCCTCA CATCTGGAAT TGGCCTTGTT AGGGGGCCCT 420 GTGATGGGGA GAGGAGGGAG GGAAGCCTGG CTAGGTCTCA GAGCTCTCTC AGCTGAGAAG 480 TGGGGATGAT TGTCCCCCCA GTCTATGGAG TGTGGGGCTG CTGTGGACAA TGGGATCTGG 540 GCCTCTGCTG GGAGGTGTTG ACCTCAATGC CTCTCTCCCT GCCTGACTTC AGTGCTCTCT 600 GTATCCTGAT GGAGACTTTC TGACAGCGCA GGGGGTGGGT TGTGGGGTCC TGCTGCCTGT 660 AGAGCTGTGT GTGAGCTCCT CAATGGCCCA AGGGTACACA GGGGTCTCTG ACTGTACCCT 720 TCCTCTTAGA CCTTGTGCCA GTGGGGAGTG AGAGTGTACC AGCCCCTCCC TCTGGGCACT 780 CCAAAATGCA CCCCTTGGAG AGAGAGTACA CCCCTCAAAG TTCATTTCCC ATTTCCTGTG 840 AGTCAGGTCT CAACCTGACA GGCATCCTCT CTCACCTCCC AATCACCATT TCCTTCCACC 900 CTTTCCCCCT TTCCCCCACT TAATCAGAAT CTGCCCCCAC CCCCACAGAG TGACTTCCCC 960 TCCTGGCTCC TCATTCCCCC TGCAGTGGGG AGGGGCCAAC ATCCCCAGCT CCCTGCCTCC 1020 CTGCAGACCC TGTCTTCTCC CCTCTGCCCT TCAGGGAGCC CTACCCCATC CTGAAGTACT 1080 CCACCTTTCT GAGTCCCCTC TCCAACCTGG GGTTCAGTGT CCCAGGGACC CCACCCCCAG 1140 CAAACTTGGC TCCTTTCAGC TCCCCTCCCT TGCGGGCAGA GGCAGGGCGT TCAAGCCCAT 1200 TTAATCTTGG CAGAATGCAA TTTCCTGCTT CAGGGAGCTG GCGGGTTTAG GAGGCTTAAT 1260 GAGGGGGGAG GGGGAGACAG GGAAGAAGAG AGGCTGAGAC GGGGCTGGGA GATGGAGATG 1320 GAGAGTCCCT GAGAGGGGTG GTTGAGGAAG TCTCGGGGAT GCGTGTCTTT GGGGGTCACC 1380 CTGGGGTCCT TGGGATCACA CAGGGGTCAG CTCTTCTGTG TCAGCCTCTC ACTGGTAGGT 1440
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