Tag | Content |
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EnhancerAtlas ID | HS176-18001 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr18:45529070-45530560 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TCF7L2 | MA0523.1 | chr18:45530373-45530387 | TCCCTTTGAAGTTC | - | 6.4 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_34739 | chr18:45527302-45532138 | HeLa |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH18I048001 | chr18 | 45528248 | 45531666 |
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Enhancer Sequence | CACAGGCCAT GTGTGTGGTG TGTGTGCATG TGTGTGTGTG TGTGTGTCTG GTGTGTGGGG 60 AGGGAAACAC TGGCTGTTTG AGATCCCTGA GCTGAGGAAG GTGAGCACAG AGTGAGCAGC 120 AGTTGAAGGT GCCCCACGCT GCCCAGTTTG GGGATTCCAA GCAGGAGGGC CCGGGAGTAG 180 CTGTCCCACT GACTTGAATG CACTTCAAGC CCTCTCTTGT TTCCCTAGGG CCGAGCTCTC 240 TTAGCCTCCC AGCCCCAGTT TCAGGCCTCC TGGGTGGCAT CCTCAGCTCA CCTGCTGACT 300 CCTTCTCTTC ATCTAGGCCA CTTCACTCCC TCTGGCCCCT GCTCAGTGCC TGGGCCTCGG 360 CCTGGTGGCC TCTGGCCTGG CCAGGGGCAT GCGGATGGCA GTGGCATTCC AGCAAGGGTG 420 AGATCACCAC CCATCGCCCT GGAGAACAGG CTGCCAGGGG AGGTGTCTGC GTCACTTGTG 480 GCCTTGTTGG CAGATCATAA AAGCTGGAAA TGCCTGATGA GGTAATTGTG CCCCAGGGCC 540 CTGGGGGCCA GACCCTGCGG GCTCCCTCCA TGGCTGCCAC TTCCCATCAC CTCCCTCTGG 600 AGAGGCAGAG TGAGCAGGCT GCTTTTCTCT TCTTTTGCTT CACTGTGGGC CCCCTTCTGG 660 CCCCTGGGAG GAGAGGGCAG AACCTCCATC TTCATGCCAG GGAGCCCCAG CTCCCCAAGT 720 CTTTGCCAAC AACTCTGAGA CCCTGCCCTG TGGGGCCCTC CTCCAGGAGG GTCCAAGTAG 780 CTGTTCCGTT GATACAGAGG GGTGTGGAAG AGTAGGGAAG GGGAAGCAAT AAATAAAATA 840 ATGCTGATGT AAGAGGCTTG GTTTGAGCCA AGCTGCCTGG GAGAGACCCA GAGTCTAGAG 900 CTAGTGTTGC TCACTGGCAG GGCTTGTCCA TGCCTTTTCT GACTCTCAGT TTCCTCATCT 960 GTGAAATGGG TGTGTTGGCC TAGAAACGAG GATCTTAATC TGCTGGGAGT GCAGATCCCT 1020 CTGAGGCTAG AGGCAAAACC GTGAGAACAT GAATTCTAGA GCAGAAGGCT GACGCCTTTC 1080 CTTGGATGCT ACCGTCAGGT CCCCAGTGAA GTTGGGTCTT TAAAATCCTG CCCCACCTAA 1140 CAATCTCTGT TGCTTGAAGG TCACCAGGAA ATGACACAGA AGCCTTTGGA GTGGTGCCCA 1200 AATGCTCACG TAGGCCTGCA CCCTGCAGCT CTGAGGGCCC AGCCCCTAGG AAAGGGAGGG 1260 CAGTAGTTCC ATGTGCTTCT CAGAAGAGCT GGTGCCAACA GGGTCCCTTT GAAGTTCCTG 1320 CTTAGGTCCT GGGCCCCAAA AGGAATGGCA CAAAAAGACA GCCCGTCCCC GTCCTCCTTA 1380 TAGCCTCATG GTGCCTGGTG CCATAAGATG GAGTGACGCA AATGTTCAGG CTGGGGAGGA 1440 AGTGTTGGGT CCAGTGTCTG AGGTCAGCCA CATCACAGAG GTTCTTGCTC 1490
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