Tag | Content |
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EnhancerAtlas ID | HS110-04132 |
Organism | Homo sapiens |
Tissue/cell | KATO3 |
Coordinate | chr6:36992150-36993560 |
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) |
JUN(var.2) | MA0489.1 | chr6:36992569-36992583 | GTGAGTCATCCTTT | - | 6.11 | ZEB1 | MA0103.3 | chr6:36993488-36993499 | CCCACCTGCCC | + | 6.14 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_61011 | chr6:36971402-37041202 | HBL1 |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I037022 | chr6 | 36990556 | 36993606 |
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Enhancer Sequence | TTTCCTGAGC GTGACTGTGA CACCGTGGAT AGGTAGAAGG ATGCCCTTGT TCTTAGGAGA 60 CCACCAGCTA CATATTTAAG GGTGAGGTGT CATGATGACT GTAATTTATC CTCAAATGGT 120 TCAGAAAAAA ATAAAATACA TACATATAGA GAGAGACAGA GAGCAAATGT GGCACAAATG 180 TTAATAATTA GTGAATCTAG TGGGTGGTAT CATTGTATTA TTTGTTCAAT TTGTCTGTCG 240 GTAGGAAATT TTTCAAAATT AAACGTTGGT AGAGGAAAAA ATATTTACTA ATTATATTTA 300 AACATTGAAA TCGCTCAATA AAAAAAAAAT GCTCCTGAGG TAGCTGAAGC CCCCGTGTGG 360 GGCTGTGCCC TGACCGTGGG TTTCTCTTGC CTGTGCAGAT CTTCGTGCCT GCTGAGCCAG 420 TGAGTCATCC TTTCGGTGGT TCGGGTGCCA GTTTCTGTCT CCCCTGCCTG CCAGACGGGA 480 ATCCTTGTGA GGGTGGGGCA GGGCCAGGCC TTCTTCTCCA GGTCCCTGCC AGGCCACACT 540 CTGTGCTGGG CACACAGAGG AGCTCCCTGA AGGCTGGTGC CGCCTGATGA ACTACACTCC 600 CTCTGCCCCT TTCTCCTGCC CTCCATCTCC ACGCCCACAT CTGGGCTCCC CATAAAGCCA 660 AGTCTTCCTC GCAGTCACAC CTTGCGGCAC CCAGTGTTCC TCTCTGAGTC TTCCCAGGCC 720 CCTTTTACCC AGCCTCCCGG CATGATCCAT GTCAGCCTTT GGGGGGTGTC TTCGTGGTGA 780 GCTGAGAGTG GGCCCCGCTC CACAGAGTAC CCATGTAAAA ACAACCAGCC TATCATTTTT 840 AGGTGAAAAC ACACTTGACT CCATGATGGC GCAGAATACA AAGTCTGCCT GAATCTTAAA 900 GCTAAACTGT GGGACTTGAA AGACACACCC TGTGTGTGGA GGGCCTGTCT GCCAGGTAAC 960 AGTGTGGCTC TCAGGGTCAG GAGAGGACAA AAGCTGGGCC CTGCTTGCCT GGTGGGGTCT 1020 TTGGGAGAGT CAGGTGAGAT GGCGGAGAGG ACAGCATTTG GAAAAGTGAA TCAGATGCCA 1080 GTGGCCCGTC TGGGGCAAGC CCCTTGGGTT CACAGCAGCC CTCACTCGGA GGGAACCTGG 1140 AGGGGAGAGA AGTTACGGCC CTCGCGGTGG GGGCCGGGTC TTGAACCCTC AGCCTAAGAG 1200 CCCCGAGCCC GAGCTCCCCC ATGTGTCGCA GCCTCCAGGC AGTTGGGCCT CACCAGCATG 1260 GGGGAGCATC CCCGCTCTGC CTCTATTCCT CCCTCGAAGC TTTCTTTTCC TCCCCCAGTC 1320 CCTGGTTGCT CTCATGCCCC CACCTGCCCA CCAAGGCAGG AGCCCAGCCC TCCGGTGCCT 1380 GGTCTCAGCC CCATGCCCCC TTATGTGTCC 1410
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