Tag | Content |
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EnhancerAtlas ID | HS145-11069 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr18:46499800-46501450 |
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) |
ESR1 | MA0112.3 | chr18:46501154-46501171 | AAGGTTACCTTGACCTT | - | 6.6 | EWSR1-FLI1 | MA0149.1 | chr18:46500760-46500778 | GGGAGGAAGGAAGCAGGC | + | 6.35 | EWSR1-FLI1 | MA0149.1 | chr18:46500756-46500774 | GGGAGGGAGGAAGGAAGC | + | 7.39 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_26908 | chr18:46499655-46503163 | Esophagus | SE_46295 | chr18:46501091-46502240 | Osteoblasts | SE_52478 | chr18:46499708-46500779 | Small_Intestine | SE_52478 | chr18:46501048-46503230 | Small_Intestine |
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| Number: 1 | ID | Chromosome | Start | End |
GH18I048973 | chr18 | 46499603 | 46503284 |
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Enhancer Sequence | TTCCCAGAAC CACAAGGTGT TCCGGACTCA TCTTCAGCAT TTCCAGCCCC AGTCCTAGGA 60 TCCGCCATTT TTGAACATTT TGAACAGAGC AGACTGGCCA CTTTTGACCC CTTTTTCCAT 120 TAAGATGTAG GTAGTTCTCT TGCGGGAAAG AACCCAGCCT TATTATCTGG TGCAAGCCAG 180 TCAATTGCAA GTAACTTGAA AGGGAGTTCA GTGTTTTACA GGGTGTTTGT TTCCATGGCT 240 GGCATAGCTA GGACCTCACC TTCAGGCCCA TCGCCCTTTC TCTCAAAAGG TTTTCAGTTT 300 GCTAGAAGCC ACTTTCCTCC CTCACTTTAC TTAGATTGCA ATGTAGACCC GCCCCAAGTG 360 AGTCAGGCTA AGGAGTTGAG AGAATAATTT AGAGAGGCCC TCTTCTCCTC CTGCAAGTCC 420 TTTGACCTGC CAGCCTGCAA ATCTGCTATA TAAAGATAGA TAAGTAGCCA GCTAGCTACA 480 CACACACACA AACACACACA CACACACACA CACACACACA CACACCCATA TACCAAAACC 540 GAGAAGGCTA CGGAGAGAGG GCAGTGGAGG CATTCACTCT GAGAATTACT GTTCAAAGGG 600 GAAAAACAGG GAGGCACTTG GGCAATCCAG AAATGCAGGT CTGAGCTGGC CTAGGGTTTT 660 AGCAAAGGAG GAGTGAGTTC TTCAGAACAG GACCAATTAA AACCTTTTAA AGTAATTGTT 720 CCCCTGCCTT CTTTCAAAGT TGAGCTCTAA TCGTGGCCTT TCATTCTTCC CACCACTCCA 780 TCATTTTAAA TTAACCTTGC GATTCCCTGC AGCTGCCTCT CACCCATCAC AGACATGCTA 840 ATGCACGTGT GTGCTGCTGG GGGGCGGTGG GAGGGGACCC TGACACTAGC TTTGTGAAAC 900 AGCATCCCTG TGGGCTCTGT TCCACTCACC CCCCTACCCA CCCTGGCAGA GCAGAGGGGA 960 GGGAGGAAGG AAGCAGGCAG GTTAGCAGAG CGCAGGACCA GGCAGTAAAG TCTCCTAGCT 1020 GCGCTACCTC GCTACCTCGG GGTGTCCACA TTACTCAGCC CCTCGGAGCC ATGGGGGTGG 1080 GGAGGGCAGG GCCTCCTGGG ACAGGACCAT AAACCGTTTA TGAATCCCTA AATGTCACAC 1140 ATCAAGTCGA CATCACCTGT TCACCTTCAT TCTTCTCTCC CTTTGTGAAA AGTCTCTCTT 1200 CGCATTCCCT CCGGGCCTCT CCCCTCCTGA CCCTTTGGAG TAGGAGCCTT CAAAGCCCTG 1260 AAGGTTCCCG AGTGATGTGG GAAGTAAAGT TCTCAATGGA GGTCTCCTCC TAGTGAAAGG 1320 GCACTCTGTA CTTAATGGAA CTGGCCAGAC CGTGAAGGTT ACCTTGACCT TGTCTGCATG 1380 ATAAATACAA CTGGAGCGGG GCGGAAGGCA CACCATTCAG AAAAGCAAAC TGCTTGCATC 1440 TTCTTTATTT TTAATCTCAC TCCATTTTGC TTCTCTGCAG GATCAAAGCA AGTTAAGGAG 1500 AGACAGCCTC TGTCTTTCAA TCCTAGGGGC AGCTCGTGCA GTCGCCCCGC CGCGGCCACT 1560 CTCCTAACAC GGGCAGAGGG GGCAGCGACG TGCCCCGGTC GCTCAGCCAG CTGGTGGCAG 1620 GGCTGTGACG GCAACCCAGG CCCCCAGACG 1650
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