Tag | Content |
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EnhancerAtlas ID | HS098-10496 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr11:68903280-68904720 |
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) |
Sox3 | MA0514.1 | chr11:68903449-68903459 | CCTTTGTTTT | + | 6.02 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_32040 | chr11:68902066-68903637 | Gastric | SE_32040 | chr11:68903789-68906652 | Gastric |
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| Number: 2 | ID | Chromosome | Start | End |
GH11I069135 | chr11 | 68902067 | 68903637 | GH11I069137 | chr11 | 68904510 | 68906536 |
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Enhancer Sequence | CCTCCAGGAG GAGCAGGCCT GGGCACAGAC TTCTGACCTG GGCACAGTTG GGAAGGGTGA 60 CAAGGGGTCA GAGCAGGCTC TTGGCCTCAG GTCAAAGGAC AGGAGTCCTC CTGACTCTGC 120 TGTGTCTGAA GCCCACAGTG AATGCAATGC AGAAAAAGCA GTGCTTGACC CTTTGTTTTC 180 TCCGGGGTTA GGATCCCTGA TATGATTGGG CTGTGTCCCC ACCCAAATCT TGCCTTGAAT 240 TGTAATGATC CCCACATGTC AGGAGTGGGG CCAGGTGGAG ATCATTGAAT CACGGGGGTG 300 GTTTCCCCTG TACTGTTCTT GTGGTAGTGA ATAAGTCTCA TGAGATCTGA TGGTTTTATA 360 AAGGGGAGTT CCCCGGCACA TGCTCTCTCT TGCCTGCCCC CATGGAAGAT GTGTCTTGCT 420 TCTCCTTTGC CTTCTGCCAT GATTGTGAGG CCTCCCTGGC CATGTGCAAC TGTGAGTCAA 480 TTAAACTTCT TTCCTTTAAA AATTACCCAG TCCCAGGTAT GTCTTTATTA GCAGCATGAG 540 AACAAACTAA TGTGATCTCA CAGAGAGCAG CGCTGGTGGT CAGAAGGAAG CTTCTGTGTT 600 TGAGGAGGGA CACTCAGGTC CCACCCCAAG CCCATGCCGT GACCTGGGGC TGCAGTTATT 660 TTGATTCCCA TTATGTGGGG AACCAAGACC CAGAGAGGGA GGACACTTGC CTGGGACTGC 720 CCAACTTTGG AAGGAAGATC CTGCCCCTCA GTTGGGGAGG CCTGGATGGC ACTGGCGGCC 780 GGGGAGGTGC GGCAGGAGCG AGGACTGATG GGTGAGTGCA GGCTGCATGC AGCCTTGCTG 840 GGACCTTGTG GGAGGGGAGA CCCTGAGTCC TGATGGGAGT TCGAGAAACC CAGGACCAGC 900 AGAGGTGAGG AACAGGCCTG GCCTGCTTTC CTCCTGTCCG TGAGCTGGCC GTGGGTTCCA 960 CCGACACGGC CCTGCCCTGG GACCTTGGTG GACAGGCAGA GAGGCTGTGT ATACATCAAT 1020 GGCCTGGGTT CCTGCAGGGC TCAGGGTCCC CTGGTCTCAG CAAGGGCCTC AAGAATGGCT 1080 GGAGAAGGGA ACACACCTTT GTCAGGGACT GTCCAGCTGC CAGGCTTGGT GCTGCAGCCT 1140 CTCCACCTGC AGCCTCACCA ATCCCTCCAA GCTGGGGTTT CTCCACTGTG GTGGCACTAT 1200 CCACATTTTG GACAGGGTAA TTCTTTGTGG AGGCTGTCCT GTATGTTGTA GGATGTTCAG 1260 CAGCATCCCT GGCTTCTATC CACCAGATGC CAGTAGCACC CCCCGCAAGC CCTGCCCAGC 1320 ATGACAGCCA AATATGTCTC CAGACATTGC CAAATGTCCC TCTGTGGGTC CCCTGGGTGA 1380 GAGCCACTGC TTGCCATCAC TCCGCATTTC GAGAAGGCAA ACTGAGGCTC TAGAGAGGCC 1440
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