Tag | Content |
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EnhancerAtlas ID | HS026-10871 |
Organism | Homo sapiens |
Tissue/cell | CNCC |
Coordinate | chr14:96632300-96633700 |
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) |
TEAD1 | MA0090.2 | chr14:96632544-96632554 | ATGGAATGTG | - | 6.02 | ZNF263 | MA0528.1 | chr14:96632844-96632865 | GAGGGTGGGGAAGGAGGAAGA | + | 6.38 | ZNF263 | MA0528.1 | chr14:96632850-96632871 | GGGGAAGGAGGAAGAGAAGGG | + | 6.97 | ZNF263 | MA0528.1 | chr14:96632856-96632877 | GGAGGAAGAGAAGGGGAAAGA | + | 7.34 | ZNF263 | MA0528.1 | chr14:96632853-96632874 | GAAGGAGGAAGAGAAGGGGAA | + | 8.81 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_39194 | chr14:96632202-96634436 | IMR90 |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I096166 | chr14 | 96633047 | 96634378 |
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Enhancer Sequence | CCCAGCTGTA AGCGACTGCC TGTCATAAAG AAGCCAGGGA AGATGAAGCC CAAACCACGG 60 GACTTCGCAA GCACTGCTCT CTGGCCACAC GCACTGTTCC TGTAACACCA CATCAAGACA 120 CAGGGGAGCT TAAAACCCTG ACCAGAGGGG TGGCATGGCC AAATACCTTT GCAGCCTGGA 180 TCGCCTGCCT GGGGCAGAGG AATCCTTAAG CATGAATATG GAACAAATGT TCTTATGGCC 240 AAGGATGGAA TGTGACAGCA CAAAGAAACA CTGGGCTGTC ACTTCCCTTC CAGGCTGGCA 300 CACCTCTCTG TCCAGGAAGC CAGGGAACAC GTGGTTCTAT GCAACCCAAC AGGAGACTGA 360 TGTGGGCTCT GTATAGGAAT ATAGGAACCC CAGAGAGGTG GAGCTGCCAC TTGCAAACAT 420 GTCTCTCTAC CAAAGGGGAA AGATCGTGTT CTATGAGAGG CCCTTCTGTC CTGCAGAGTA 480 CGGGGTGGGT TTGGACAGGT AAATATGGGC TGGGGAAGGG TAGATTGCCC TGAGGACCTG 540 CAGGGAGGGT GGGGAAGGAG GAAGAGAAGG GGAAAGACAG AGTCATGAAT TTGTAGAATG 600 GCAGGAAGCC AGGACTCTAG GCTGGCAGGG AGAGACCCAG TGGAAAGTGG CCAGAGGGTT 660 TTATAGGCGG GCACGGCTGG TGGCATTGCT GCAATGCACA CCTCCACCAC CTTCTCCCCA 720 GACCTTCAAG AGAGTGGGCT ACACACTCTC AATGTGCAGG GTTGTCCTAT TTCTTTTGTT 780 TGTGGAAATG GGAGAGTCGA GTTCCACGTT GAGCTTGACA CAACACTGGT GAGACACGGG 840 GCAGCGAGAT AAGCCCTAAA TTGGAAGCAG ATGCTTGGGG CCACAGGCAT CCTTGGGAAC 900 TTAAACCCCC AAGACATCCT GGAAAAAGCC AATCGTATGT AGGTTGCAAG AGTCAGGGAA 960 ATCTCTGCTG ACTGCAGGCC CACGTCATGA AAGTCTCTCT ATCACACATG CCCACACACC 1020 TGGCCACCCC CTAGTGCCAG GTCAGAGTCC CTCTGTGAGT GCCCACTTGC ATTGTGCCTA 1080 TGACTGCCAC TGGGCCACCC ACCACACCAT GTCATCATGG CCAGTTCACT TCCCTGCCTC 1140 CCTGTTCAGT CTCTGGGATC CTCAAGGCCA GGTACTGCAT GCTAATCATC TCAGACACCC 1200 CACCACCTCG CTCAAGCCTC AACAAAAATT GGCGTTGGGT GGAAGAGAAC TGGATGGACA 1260 CTTCTGGAGT CTGACATTGT GCCAGGCTCT GAGGGTACAA GTTGACTAAG ACCTGCAGCC 1320 TGCTCACAGG GTGCTCAAGG GCTCAGTGAG ATGGGTGTTC TAAGAGGCAG TGAGGTCCTC 1380 ATCCCTGGAG GTAGGGAGGT 1400
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