Tag | Content |
---|
EnhancerAtlas ID | HS037-18002 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr19:38613110-38615570 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GLI2 | MA0734.2 | chr19:38613768-38613783 | CACCTTGGGTGGTCT | - | 6.25 | REST | MA0138.2 | chr19:38613627-38613648 | CTCAGCACCTGGGCCAGCATC | + | 6.93 |
|
| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_65256 | chr19:38612554-38613976 | Pancreatic_islets |
|
| Number: 1 | ID | Chromosome | Start | End |
GH19I038121 | chr19 | 38612555 | 38613976 |
|
Enhancer Sequence | GCCACCCTGG TCTCTCCCGG ACACTTTCGA TGGTGTCCTT TCTGGTCCTT CTTACCCCTG 60 CCCTTGCTTC TCTGTGGCCT GTTCTCGACG TGGTAGTGAG AGCAATCTGA TCACATCACC 120 TCTCTGCCTA AACCCTCAGG TCACTCTAGG TTAAAGCCTC AGTCCTTACA GAAGCCCATG 180 AGGCCGGGTG TGAACTGGCT CCCTGTCGAC TTCTCTGACC TCATGTCACT GTTGCGCTCT 240 CTGCCCCAGC CATGAAGACC TCTGAGGTTT CATGCGCATG CTAGGGCGGC GTCCAGCCTC 300 AGGGCCTTTG TACCACCTCT TGCTGGAACA CTTCTCTGAT CACCACATGG CTCGCTCCCT 360 TTCCTCCTAC AGGCCTTTGG TCACATGTCG CCTTGTCGGT GAGGCCTCGT TATCTAAGAT 420 TGCACACCCC CTCCCCTGGC TTGGAGCACA TTCACGCGCT TTGCCTGCTT AACCACCATC 480 TGCCATGCAC TGTGTGTTAT CTGTTCACTG CCGTGTCCTC AGCACCTGGG CCAGCATCTG 540 GTGCACAGTA GCCGCTGAGT GAGCAGGAAC CGAGTGCAGG CACAAATGCG TCGTATGCTA 600 TAGTGGCCGC AATAGTGAGG ATCAAATGGG CGCCAGCTCT GCGTCAGACC CTGCTCAGCA 660 CCTTGGGTGG TCTTGCGTCT CTTGCTCACA AAAGCCTGAT GAGGTCCTCA CTTCGCAGAT 720 GAGGAAACTG AGGCCCAGAG ATACCTTGAC TTGCCCAGAG CCCAAAGAGC CTGGGTTTTG 780 GAGTTTTTTT TTTGTTTTTT TTGTTTTTTT TTTAATTGAT CATTCTTGGG TGTTTCTCAC 840 AGAGGGGGAT TTGGCAGGGT CATAGGACAA TAGTGGAGGG AAGGTCAGCA GATAAACAAG 900 TGAACAAAGG TCTCTGGTTT TCCTAGGCAG AGGACCCTGC GGCCTTCCGC AGTGTTTGTG 960 TCCCTGGGTA CTTGAGATTA GGGAGTGGTG ATGACTCTTA AGGAGCATGC TGCCTTCAAG 1020 CATCTGTTTA ACAAAGCACA TCTTGCACCG CCCTTAATCC ATTAACCCTG AGTGGACACA 1080 GCACATGTTT CAGAGAGCAC AGGGTTGGGG GTAAGGTCAC AGATCAACAG GATCCCAAGG 1140 CCGAAGAATT TTTCTTAGTA CAGAACAAAA TGAAAAGTTT CCCATGTCTA TTTCTTTCTA 1200 CACAGACACG GCAACCATCC GATTTCTCAA TCTTTTCCCC ACCTTTCCCC CCTTTCTATT 1260 CCACAAAACC GCCATTGTCA TCATGGCCCG TTCTCAATGA GCTGATGGGT ACACCTCCCA 1320 GACGGGGTGG CGGCCGGGCA GAGGGGCTCC TCACTTCCCA GTAGGGGTGG CCGGGCAGAG 1380 GCGCCCCTCA CCTCCCGGAC AGGGCGGCTG GCCGGGCAGA GGGGCTCCTC ACTTCCCAGT 1440 AGGGGCGGCC GGGCAGAGGC GCCCCTCACC TCCCGGACGG GGTGGCTGGC CGGGCGGGGG 1500 GCCAACCCCC CCCCACCTCC CTCCCGGACG GGGCGGATGG CCGGGCAGAG GGGCTCCTCA 1560 CCTCCCAGTA GGGGCGGCTG GGCAGAGGCG CCCCTCACCT CCCGGACGGG GCGGCTGGCC 1620 GGGCGGGGGG CTGACCCCCC ACCTCCCTCC CGGACGGGGT GGCTGCCGGG CGGAGACGCT 1680 CCTCACTTCC CAGACGGGGT GGTTGCTGGG CGGAGGGTCT CCTCACTTCT CAGACGGGGC 1740 AGCTGCCGGG CGGAGGGGCT CCTCACTTCT CAGATGGGGC GGTTGCCAGG CGGAGGGTCT 1800 CCTCACTTCT CAGACGGGGC GGCCGGGCAG AGACGCTCCT CACCTCCCAG ACGGGGTCGC 1860 GGCCAGGCAG AGGCGCTCCT CACATCCCAG ACGGGGTGGC GGGGCAGAGG CGCTCCCCAC 1920 ATCTCAGACG ATGGGCGGCC GGGCAGAGAC GTTCCTCACT TCCTAGATGG GATGGCGGCC 1980 GGGAAGAGGC GCTCCTCACT TCCTAGATGG GATGGCAGCC GGGCAGAGAC GCTCCTCACT 2040 TTCCAGACTG GGCAGCCAGG CAGAGGGGCT CCTCACGTCC CAGACGATGG GCGGCCAGGC 2100 AGAGACGCTC CTCACTTCCC AGACGGGGTG GCGGCCGGGC AGAGGCTGCA CTCTTGGCAC 2160 TTTGGGAGGC CAAGGCAGGC GGCTGGGAGG TGGAGGTTGT AGCAAGCCGA GATCACGCCA 2220 CTGCACTCCA GCCTGGGCAC CATTGAGCAC TGAGTGAACC AGACTCCGTC TGCAATCCCG 2280 GCACCTCGGG AGGCTGAGGC TGGCGGATCA CTCGCGGTTA GGAGCTGGAG ACCAGCCCGG 2340 CCATCACAGC GAAACCCCGT CTCCACCAAA AAAATACGAA AACCAGTCAG GTGTGGCGGC 2400 GCGCGCCTGC AATCGCAGGC ACTCCGCAGG CTGAGGCAGG AGAATCAGGC AGGGAGGTTG 2460
|