Tag | Content |
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EnhancerAtlas ID | HS098-23622 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr17:27407920-27409330 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GLIS2 | MA0736.1 | chr17:27408647-27408661 | CTTTGTGGGGGGTG | - | 6.22 | GLIS3 | MA0737.1 | chr17:27408647-27408661 | CTTTGTGGGGGGTG | - | 6.73 | ZNF263 | MA0528.1 | chr17:27408493-27408514 | GGGGGAGCTGGAGAAGGGAGG | + | 6.09 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_63416 | chr17:27369672-27424111 | NCI-H69 | SE_65361 | chr17:27408025-27408997 | Pancreatic_islets | SE_65361 | chr17:27409187-27414446 | Pancreatic_islets |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I029081 | chr17 | 27408026 | 27408997 |
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Enhancer Sequence | CCCCGATGGA GTCCTTTAGG GTGAGCCGCT TCCGATAGCT CAGGGAGCTC ACCACCGAGG 60 ACGGCCTCTC CTCCACCCCC GGGGCCTCCT TAGAGAGGCT GTTGAGGGCC GTTCCGAGGG 120 AGGATGCGAG AACCAGACGT GGATGAGGGC AGCAGGGAGA GAGGGAGGTT GAGAGAGAGA 180 GAGGAACAAG TATTAAACTC AGAGAATAAA GACACAGGGG GAGGGAGGCG AAAGGAGGAG 240 AAAACGGCAG CAGCCCTGGC AAAGTGGTGG TGAGAGCATC GGAGGAAATG AAGCAAAATA 300 ATTTGCGTCA GTGAAAATAG CTTCATGGAG AATGTCATGT AAATTAGACT ATTGTTCTAT 360 TTCATCACTT TTCCCCCTCT AAACGTTTAG TTCAATTTAT TTCATTGTCA ACTACCTGGA 420 GCCTCGTGCC ATGCCGTGGT GAACCACGGC AGTGGGGCGG GGAAGCCGGC ATTATCTGCA 480 ATAACAAAAT GTTGTTTGGC CGAATAAATT AAACCAATTA GAGGGGGCTG CTGGGTGCTT 540 CTGGTGAGGG GCCAGGCTTG GGGAAGGGGC CTTGGGGGAG CTGGAGAAGG GAGGGAGAGA 600 TGTTACTTTT TCTACCCAGT CTACCTGCTG TCTCTGGGAG AGGATGAGGA AGGGTGTGTC 660 CTGGAGGATC AGGATGGGCT TGATCAGGGG GTTGGGATTC TATGTTGTGG GGGCAGCAGG 720 GATATGGCTT TGTGGGGGGT GAGGGGGGAG CGAGGGCTCT TCTTTCTCCC TGCTGCCACA 780 CTGGCCAGTA GGAAAGAGAT GGGCAAGGGG AAGCTCTGGA TTCCAGGGGT AGCTGTCTGT 840 ATGATCAGAG GACTATGACT GGCTAGAAAA CAGGGGAGTA CATTCCCCCA GTGGATGGGT 900 ATTAGGAGGA AAGAAGTGGG GGCAGTGAAG AGATTAGAGG AAGGAGAGAA TGGGCAGAAA 960 AAGACAGAAA TGTGCCTGTA ACTGGGTCAA GAATCAGTGG AACTGGTGCC TCTTCTGCTG 1020 CTATTCACGG TAAGACGTCA GAGATCCAGA GCTGGCCAGG GCTGTGGGAT TAAGAGTCCC 1080 CTGTGCCCCA TCCCAGTTTT GATTCCAAGG GTCTGAACTA TCAGGAAGCT TGATCAACAT 1140 TTGTTGAATG AATAAGTGGA GGTGACATTT AACTTACATC AAACCAAAGC CTGGAGCCTA 1200 ATGGGAAAAC ATTCCCTGGA AAAAATAAGG GCGACGCAGC CCTGGCTAAG AAGAAACTTC 1260 CTGTGCCCAT GCACATGCCA GAAGCATGCC CGGGCCGCAG TCACAAATGC CAGACAAGAG 1320 ACACAGGCCT GCCCTCATGG GATCCAGGCG CTACTTGTCC ATTCCTTGTG GCACAAGGTG 1380 GCTTTTCCTC CCAGCTCAAG GCCATATGCT 1410
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