Tag | Content |
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EnhancerAtlas ID | HS041-04098 | Organism | Homo sapiens | Tissue/cell | EWS502 | Coordinate | chr11:68746100-68747150 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gfi1b | MA0483.1 | chr11:68746522-68746533 | GGCTGTGATTT | - | 6.02 | NR2F1 | MA0017.2 | chr11:68746893-68746906 | CAGGGGTCAAGGG | + | 6.22 | ZNF263 | MA0528.1 | chr11:68746591-68746612 | GGGGGAGGGAGGAGAGTGGAG | + | 6.46 | ZNF263 | MA0528.1 | chr11:68746583-68746604 | GAAGGAAAGGGGGAGGGAGGA | + | 6.75 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr11 | 68746793 | 68747129 | chr11 | 68746202 | 68746252 | chr11 | 68746306 | 68746854 |
| Enhancer Sequence | CAGTCTTCGA GTCCCCAGGA CACCATCACC TGCCACGGCA CAGAACCGCA GGCTGTGAGA 60 GTTGATTCCA GGGGTGTATT TTATAGCTTA CTGATGAGCT GTCCTCTCCT GTCTCAGGAT 120 CTGACCTGTG CCCTGGCTGG CTCGAAGGCT CCATCTTTTG GGAGGAGACT GAAAACTGCT 180 TCAGAAAGAT GCCAAGAGAA AGAACAAGAT CATTTTCACC TTCTGACATG AAAAACAGGA 240 TGACGCAGCC AGGTGCCAGG CTTGCAGGCC AGGCTGTGGT CTGGAGACAG GATCTTTCCA 300 CTTCCGTCTT TCCTCCTCCC TCACCTCTTT AAGTCCAGGA CTGACTCTGC AGGGACCTCC 360 TGTCTTGCAC CCCCTCCATG CAAGCCCCGA GCCTCGAGGC TGGATGCTGG GTGGTAGGAA 420 AGGGCTGTGA TTTGTGGAAA GTGCAGGAAA CATCTGCCTT GTTCTGGACC CAGGGGACTG 480 TGGGAAGGAA AGGGGGAGGG AGGAGAGTGG AGCCAGCTGA TGTGTGTCCC AGATGTTCCG 540 TCTTTGGGCT TTTGGGCAAA GTGAGGGGGC CCTGGGAGGG ACAGTCAGTG AGGTATGAGA 600 CTCTGGCTCT GGGGGACACT GCCTGGAAGG CTGCCCTCCA CTGCCTGGGG CACTGTCCTA 660 TCAGCATCTG CTGGAGTGAC TGCCAGTGAA GCCAGGCAGA GGCTCTTCCC TTCCCAGTGC 720 GGCCTGGAGG AAAGCGAACA GGCCTGCCCT GGGTGCGAGG GGTGACAGGG TAAGGCGACC 780 TCATAGCAAA TGCCAGGGGT CAAGGGCTGG CCAGGGGTCA GAGGGATGGT GGGGCAGAGT 840 CTCATGGCCC ACAGCCAGCG AGATCCGGGT CGGCGATGGC GACACCGTTT ACTTGCCAGA 900 CTTCAGGCAC ACCTGGGGAA AGGTGCACGG GGGCACCACC TTGGTGGCCA GTTGATGCCA 960 CCCAAGGACC AGCATAGGGC CAAAGATCAC CCGAGGTCAC CTGCCTCCTC CACAAAGATG 1020 CCGTCTTAGG CAGAGAAGGT GGTTGGGAGA 1050
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