Tag | Content |
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EnhancerAtlas ID | HS110-03662 |
Organism | Homo sapiens |
Tissue/cell | KATO3 |
Coordinate | chr4:1016260-1017420 |
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) |
NR2F1 | MA0017.2 | chr4:1016281-1016294 | CAGAGGTCATGGG | + | 6.22 | PLAG1 | MA0163.1 | chr4:1016759-1016773 | GGGGCCCTCGGGTG | + | 6.31 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_57242 | chr4:1016075-1016576 | VACO_400 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH04I001022 | chr4 | 1016076 | 1016576 |
|
Enhancer Sequence | TGGGTTAGTC GCTGCTGCGG TCAGAGGTCA TGGGCTGGGT TGGAGCCAGG CAGGGGTGTG 60 CAGGAGGGCG GACGGGGACA CACCTGGGGC CCGAGAGTCA GCCAGCCCCC GGCAGAAAGC 120 CTTCCTTCGG TGCCCTGCCC CACCTCAGCT GGCTGCACCT CTGCCACCAT CCCCCAGGTA 180 TCCTGTCCCG TTCCTGTCCC CGTCAGGCTC CAGCCTCGGA GCCTTCCTCC CAGCGGAGGG 240 CGGAGGGTGG AGGGCGGGAG CCGAAGGCAG TGGTCCCACA GAAGGGCTGG GGCCCGAGGC 300 CTTGGCAGGG TGTGCCGGCC GTCGGCTGTG ACTTTGAGGC TCGGGTTTCG GAGTTCAGAG 360 GAGCCGCCGG GATGCGTGGC CTTTCTGTTC TCTTCTGCGC CTGGGGCCCG GGCGCTGGGC 420 TTGGACAGGT GTCCAGAGAG ACACGCCCTC CATACCTAGG GACCCGGCAC CCCGCCTGCT 480 CCGCTGGGCT CCTGGGTGTG GGGCCCTCGG GTGGAGCTCC TGGGAGCTGG GCTGGCCCGT 540 TTCTTTTTTT TTTTTAATTC TACTTTAAGT TTTAGGGTAC ATGTGCCCGT TTTCTGAATA 600 CAGGAGCCTG GCCCAGGCCC CAGCAGGGTC TGGGGGTGCG GCCTGAGACA GCCTGGTCCT 660 GGGCTCAGTG AAGGAGCGGC TGTCACAGGG TGGATGGAGG GGACATTCCA CAGCACGCCC 720 TGCCCCTCGG CATTGTGTGG AATGGGAAAA CTGGCTGTCC CCCACCCCCA CCCCACAGTC 780 CTTTCAAAGG GGACGATGAC CGGGTGGTAT GAGAGTCTCG TCTGTTCACC AGCCCTCGGC 840 CCCTTGATGT AGGCTAGGGT TACTGCAGCT GCTGGCCGGG CCCGGCTCCC TCCTCCCCCG 900 GGGCCTGCAG ACCCCCCGGA GCCAGAATGG GGGCCGGCCC TCCAGCCCCA CCCGTGCCCA 960 TCAGGGTCAC CTGCGCCCAG TGTGGGCCAG CGGCCCTTGC CCAGCTGTCC CTGGGATTCT 1020 GGGCTGTGGG TGTGTGGCGC AGCCCCCTGC CTGGGTGTCC AGGGCTGTCC CGGCTGGGGC 1080 TGGGGGAGCT AGAGGCCACG GGGGAGTTGG GGGAGCTCCT CAGGGCCCCC CTCACCTGCC 1140 CTCCCTGTGC ACCTCCGTCT 1160
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