Tag | Content |
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EnhancerAtlas ID | HS183-08601 |
Organism | Homo sapiens |
Tissue/cell | T47D-MTVL |
Coordinate | chr7:1514470-1515580 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HES2 | MA0616.2 | chr7:1514886-1514896 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr7:1514886-1514896 | GGCACGTGCC | - | 6.02 | Myod1 | MA0499.1 | chr7:1515259-1515272 | AGCAGCTGTCACT | + | 6.64 | Myog | MA0500.1 | chr7:1515258-1515269 | CAGCAGCTGTC | - | 6.14 | Tcf12 | MA0521.1 | chr7:1515258-1515269 | CAGCAGCTGTC | - | 6.02 | Zfx | MA0146.2 | chr7:1514493-1514507 | GAGGCCGGGGCCGC | - | 6.15 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_23483 | chr7:1513892-1514795 | Colon_Crypt_1 | SE_24254 | chr7:1513897-1514700 | Colon_Crypt_2 | SE_25042 | chr7:1512905-1514969 | Colon_Crypt_3 | SE_25042 | chr7:1515084-1515763 | Colon_Crypt_3 | SE_27601 | chr7:1513390-1514892 | Esophagus |
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| Number: 2 | ID | Chromosome | Start | End |
GH07I001473 | chr7 | 1513341 | 1514690 | GH07I001475 | chr7 | 1515085 | 1515763 |
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Enhancer Sequence | CCAGCTGCAG GGAGGGGCGC TCTGAGGCCG GGGCCGCTGG CTCCCCTCAC TTGCCCACCC 60 ACACTCAGCC TGGCCGCCAG CTGTGGCCGT GATCCACCGC GTGGCACGCC ATGAGCAGAG 120 GAACTGGCTC CTTACGGCTT CCATGAGCAC CTCGGGAGGG CAGGCAGGCC ACAGCCAGCC 180 TCTGGGAAAA CCCCATACAG AATAAAAGCA AAGCTCCACA CCAAATGATA CAATGAGCGG 240 GAAACAAGCC AAAACTACAC ATCGGCCAAG CAGGCGCAGT GGCTCACGCC TGCCATCCCA 300 GCACTCTGTG AGGCCGCGGC AGAAGATCAC CAGAGCCCAG GAGTTCAAGA CTAGCCTGGG 360 CAATGAAAAT AGCCCTCTCT ATTTTCAAAA ATACAAAAAG AGTAACTGGG TGTGGTGGCA 420 CGTGCCTGTG ATCCCAGCTA CTCGGGAGGC TGAGGTGGGA GGCTCACTTG AGCACAGGGG 480 GTTGAGGCTG CAGTGAGCTA TGATGGTACC GCTGCACTCC AGCCTTGGCA ACAGACACCC 540 TGCCTCAAAA ACCCTCCACA AAACTGCACA TCAAGTGTGA TTTCAACAAA TAAAATGACA 600 TATAAGTGAA AAAAACCACA AGCAGAAATG ATTAGAGAAA GTCAGCTGCC CTCTGTGGTA 660 CCAGCAGAAG ACAGGCTGCA GGTTCCGGCC TGCGGTGGGG AAGCGGGTAC GGGAGGCCCA 720 GCTCTCCCCA CCAGGGTCAC TGGAGAGGAG CAGACGCAGC CGTCCGCCAA GACCCGGGCA 780 CGAGTCCCCA GCAGCTGTCA CTGCCCCAAA CTGAACGTGA CCCCACGTCC ACCAGCAGGT 840 GAACAGATAA ACCAACGGCC GATCCACACA ATGGCAGGCC ACCCAGTGCC CACAACACCA 900 CGACTCTCCA GACTGTGCGA GCAGAGCACC CGCAAGCTCC CTCGGTATAA AACTCAACGC 960 AGACAAACCC ACAGGGCCAC AGGGCGGCGC GGACTGGGAA GGGGCAAGAG GGGTAGCCGG 1020 CGATGGCCAT GTACACTGTG GCCTCCGCCC TCCCTCCCTG CCCGGCCAGG GCACCTGGGA 1080 CGGCGGCGGG GAGCGGCAGA GTTGCGCCCT 1110
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