Tag | Content |
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EnhancerAtlas ID | HS120-03481 |
Organism | Homo sapiens |
Tissue/cell | LNCaP-abl |
Coordinate | chr19:51392660-51394110 |
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) |
EWSR1-FLI1 | MA0149.1 | chr19:51392937-51392955 | CCTACCTCCCACCCTTCC | - | 6.14 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_41577 | chr19:51392340-51393349 | LNCaP | SE_41577 | chr19:51393397-51394313 | LNCaP |
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| Number: 2 | ID | Chromosome | Start | End |
GH19I050889 | chr19 | 51392341 | 51393349 | GH19I050890 | chr19 | 51393891 | 51394926 |
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Enhancer Sequence | AAGGAAATTT ATTATGCCAA AGGTGGGATG AATTTGTATC TGGAAGGATC CAGCTAGAGC 60 CAAGAAGGTT CAGCTTCAGC TTGGCTTACA CTATCCCCAG AAAAGTTCAA CTCAGCCTTG 120 TTCCCTCTTC TGTTATTTTG CTGTGCCCAG CTGGGGCCCC TCCTAACTCC AAGGGCCAAG 180 AAAGTTCAAC TTCAGCTTGG CTTACACTGC CCTCAAAAAA GTTCAACCTA GCCTTGGTCC 240 CTCTTCTGTC ATGTGGCTGT GCCCAGCTGG GGCCCCTCCT ACCTCCCACC CTTCCATCTC 300 CAGCTGGACA GGTGCAGCCT TAGTGCCCAA CTGTTTGTCA AAAACTCTGA AGGGGCTGAT 360 ATTTTGCCAA CTGGCAAACA AATAAGTTAG CCTGCCACAG TTTTATGGAT ACTGGCAGAA 420 CACACTGGAT TCTGGATCAA AGGCAAAGGA CTTTATTACT CACAGCACAG AAGACAGCAT 480 GAGCTTTGTG TTCACATCAG TTCGCCTTGA CCCTAAGTCC CACAGGAATG ATCAGAGAAG 540 TTTAGGAGGA TCCTGTGACA CGATGCTTTG ACCCACAGCT GAGAAACCTG AGCTTAGGAA 600 TCCTGAATCG TATGAAGGGA CTATTAATAT TTGTCCGAGA GGGAGACACA TTCTTCGTTA 660 TCCCGACCAC AAACAGACCT GCTCTGGAGG AACATACTAT ATTTATTGTA CTGAACACTA 720 AACAAATCTG CTTTAAGGGA CACATTATTA CACTGGTCGG TAAGCAAAGC TGTTTTGTTG 780 AAAATACCAT TTGCAAGATG GCTTGCTAGC CAAACATCCT TGATAGTCCA AAGCAATTTT 840 TTTTTCACTT TGAAGCCATG TAGAAACATG AGAGGCCCAT GGAGAATTTT CTCTCAGAAT 900 CATAATTTAA ATTCTCTAAC CTTCCCTGCA AAACAAACTT ATACTTTCTT CCTTATACCC 960 CTTGTCTGCC ACATCTGTTA CCCTAGCCTC ACCAGTGTGC CAGGCCCAGT TCCCAAAGAT 1020 GGCAGGAAAA ATATGGGGAT CTGATCTGGA TGTGCCCTAT TGTTGCTGTC TGTTTATGTG 1080 TGGATTTGAC TTTGAGGGGA CATATCCACG TTTCCCAGTG TAGAGGCTCA GGGTCTTCTG 1140 ACTGTGAAAA GTCCTTGTTT GGTACTTGTG CGTAGTGCAG TTCTGTGTGC GTGTGTGTGT 1200 GTTGTGTGTG TGTGTATGTG CATGCACATG TGTATGTGGT GGGTGTGCAA GGCCCTGCTG 1260 TCCACTACCT GCCCACACAT GTGAGCCATG TCCCCATATG GGAAAACTGA TGAGTAACCT 1320 TCAACACCAA GTGTCTGACT TGGGGGGTGA TCTAGAGACA GATAAATCTT TCCTGTCCCA 1380 GCTGCCTGTG TCTCCAGAAT ATGTCTTTCC CCATAAATGC CCAACTCTGT GTCTGGGAGT 1440 AGCCAGGAAT 1450
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