Tag | Content |
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EnhancerAtlas ID | HS105-29862 | Organism | Homo sapiens | Tissue/cell | IMR90 | Coordinate | chr16:11496540-11497880 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR2 | MA0258.2 | chr16:11496915-11496930 | GAGTCAAGCTGACCT | - | 6.07 | Nr5a2 | MA0505.1 | chr16:11496570-11496585 | GCTGACCTTGAACAT | - | 7.23 | ZNF263 | MA0528.1 | chr16:11497811-11497832 | CCCTCCTGCCTCGCCTCATCC | - | 6.12 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr16 | 11496796 | 11496959 | chr16 | 11497303 | 11497502 |
| Enhancer Sequence | AGGCCAGCGG AGCCGCCCGC TCACCCTACA GCTGACCTTG AACATGAGGA AGACCAGAAA 60 AGCTGCCCAG GTGACCCACA GCCTCGTGAG CAAGGCGCCA CGCTTGCTTT ATGCCGCTGA 120 GTTTCGGAAT ACTTTGTTAC CATCCTGAAT CAGGAGCTGA TGGGGGCAGC CGCAACCTCA 180 ACAACCTGCA TCCCTCTCGG GGGCCTCACA TGCACAGGTG CCCTGTGCCC CCTCGGAAGC 240 CCCACACCCC ATGCCACCGT CTGCTGTCCT GTGCTCTCCT TCCATCTTGG ATGTGACAGG 300 TGACACCCCA TAGCTGAGTC CTCGCAACAA CAGATGGCCT CCACACCCCG GGTTTTCTTC 360 CTCTGTCCCC CAGGTGAGTC AAGCTGACCT GACCTCCGAC ATCACTTGAC CCCATCTCCT 420 GAGGCCCCTG AGCAGCCCTG CTTTCCCAGA CCCCACAGCA GGAGGCTGCC CGAGGCCCCT 480 GTGCACGCTG GTGACCTGTG AGCTCTGTAC AAAGGGCACC CACCTGTTCA GATGGGCTGC 540 AGGAGCCGTG CCCAGAGACA CTGGCACTGG CTGGTTCTCA GGGCATCACC CAGTCATTGG 600 TTCTGGGGAG GCTGACCACA TGCAGGGCTA GAACCCTTTG TTCCTGCCAC CCGCTGACCC 660 CACCTGCAAC ACTGTCAACA CCGTGTGGGG CTGCAGACTG TGTAGCTCAC CAAGGGTGGC 720 ACAAATACAC ACACACACAG GCATGCACAC ACGTGCATGT ATACACACAC ATGCACACAT 780 ACACACATGA GCACACATAC ACTCATGAGC ACACACATAC ACGCATGCAC ACTGCCTTGG 840 CTTGCTGGGG ACCTGCTCAC TTCCTCTGCC TTCCAGGGCA CACATGTGGC AAATGTGACG 900 CTGGGAGGAT TCCATCAGGC CACCTGGTAA GCCGTGCCTC CAGGCTGGGG TCTGCACTCT 960 GTCTCCACAC CTGGCAGGCT GTGGGTCGGG CTCTGCTCTG TGCTCAGGAG GTTCCTTACA 1020 CAGAAACTAA GTCTTGTGGC TGCCCAGGCC ACAAATTACA GCCCCTTCCA GGGATGCCTG 1080 TTTCTGGAGG ACCCAGGGGC TCATGGCTGC TGTTGTTGGC GCTGTGTCGG CACTCAGCTC 1140 CCCTGGCACC ACAACTGCCC AGGGATGCCA CCTCTTCCAC GCCCTGGCCC CTTCTCCCTG 1200 CCCGGCTGCA CTCAGGATAA GCCCCAGCTC CTCTCTATGA GCTGAGACGC TGCATGACCT 1260 GGGTCCCCCA GCCCTCCTGC CTCGCCTCAT CCCTTCTCCC CATTCCAGCC ATGCTAGCCC 1320 CGCAGCTGCT GCTCCACATG 1340
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