Tag | Content |
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EnhancerAtlas ID | HS145-24253 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr7:101706940-101708040 |
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) |
BCL6B | MA0731.1 | chr7:101707142-101707159 | AGTTTTCCAGGAATTCA | + | 6.16 | EWSR1-FLI1 | MA0149.1 | chr7:101707901-101707919 | CCTTCCTCCCTCCCTCCC | - | 7.28 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_34891 | chr7:101704768-101709954 | HeLa |
|
| Number: 1 | ID | Chromosome | Start | End |
GH07I102061 | chr7 | 101704436 | 101710091 |
|
Enhancer Sequence | GGGATTACAG GCGTGAGCCA CCGTGCCTTG TCAAGAACCC TTTACATATT GAGCATTTTC 60 ATAAATATTT AAACCTGGAT TCCTGAACCC TTGGGTCACA TCTGCAGACC ATGCAGTTGG 120 CCATTGCGGA AGATATTAAA AGCATATTAA ACACCCACTG CGTGCCCGTG GTCGGGAGGA 180 AAAACAGTTG ATGCTACAGC TTAGTTTTCC AGGAATTCAG TATCCCTGAG TCAGGCAGCC 240 TTATCTGTCA TCCTAGAACT CCAGGACAGC CCCAGGTGGT GGTGGGAGGG GCCGCGGCTG 300 GGAGATGGAG CTGCTCTGAG CCTGCAGATC AGGGTAGCAT TCCTGGGAGG CGCCTTCCAG 360 GCGGAGGGGA AATTGCTCAT GTGTTCTGGG AACTGGGAGT GACTGGGTGT GGCAGGAGTG 420 TGAGGCATGG CAGGAGGTGA GCCTGAAAAA GAGGCTGATC CCTCAGAGCA GGACAGGTTT 480 TACCCAAGGC TGCAGGCCAG TGTCTAACCG TCTCTAGATC CGTCCTGGTT TAGCTTCTTC 540 CAAATAGTTT TGTGTCTGTG TGAGAGTGTG TGTGAAACGG AGTTTTGCTG TGTTGCCCAG 600 GTTGGTCTTG AACTCCTGGG CTCAAGCGAC TCTCCCACCT TGGCCTCCCA AAGTGCTGGG 660 ATTACAGGCA TGAGCAACGG TGCCGGCTCT AAATGGTTTT AAGGGCACGG TACCTACCTC 720 AAGCTAACGT GCAGGCAGGC ACGAGGTAGC TGGAATTCTA GCCTAGGATT CTCTCTTCAG 780 CAATTCTTGC CTTAAGACCT CACCTTAGAC GTTTGCTCAT TCACAGATCC CTCCCCTTCT 840 CAGAGGGAGC TGTGTTACCA AGCCTTGGCT TGTACCTCCA AGGCATGCAG TGGATGGGCT 900 GAGCTCCCTG CAGGGAGTCA GGCGGGTGTG TGGGGGGCAT GAAGGTGAGC AGGACACTGT 960 CCCTTCCTCC CTCCCTCCCA CGGATGCTCT TCCTGGCTGG TAGCCATGTG GACACCTGGG 1020 GGGAAGCTGT TCTGTGTGGC AGAGTCACTG TGTTGTGTCT GGTACTGGGG CCCTTGCCAG 1080 GGTAGGTCAG TGACTCGTCC 1100
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