Tag | Content |
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EnhancerAtlas ID | HS108-29295 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chr3:171747260-171748070 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr3:171747689-171747707 | TCCCCCTTCCCTCCTTCC | - | 6.31 | EWSR1-FLI1 | MA0149.1 | chr3:171747693-171747711 | CCTTCCCTCCTTCCTTCT | - | 7.68 | ZNF263 | MA0528.1 | chr3:171747698-171747719 | CCTCCTTCCTTCTCTTGCTTC | - | 6.06 | ZNF263 | MA0528.1 | chr3:171747685-171747706 | GTCCTCCCCCTTCCCTCCTTC | - | 6.12 | ZNF263 | MA0528.1 | chr3:171747692-171747713 | CCCTTCCCTCCTTCCTTCTCT | - | 6.45 | ZNF263 | MA0528.1 | chr3:171747689-171747710 | TCCCCCTTCCCTCCTTCCTTC | - | 7.81 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GCTCTCGAAC TCCTGAACTC CAGTGATTCA CCTGCCTTGG CCTCCCAAAG TGCTGGGATT 60 ACAAGTGTGA GCCACTGTGC CTGTCCTAGA CCTAGTTGTT AAAAAGATCC TAAGGCTGGG 120 TATGGTGACT CATACCTGTA ATCCTAGCAG TTTGGGAGGC TGAGGCAAGA GGATCACTTG 180 AGGCCAGGGG CTTAAGACCA GCCTGAGTAA CATAGCAAAA CCCCATCTCT ACCAAAAAAT 240 AGAAAAAATA GCCAGCATGG GTTGCATGCC TGTAGTCCCA AGCTACTAGG GAAGCTGAGG 300 TGGGAGGATT GCTTGAGCGT AGGAGGTAGA GGCTGCAGTG AGCCATGATT GTGCCACTGC 360 ACTCCAGCCT GGGTGACCGA GTGAGTCCCT ATCTCCAAAA AGATAAATAA TTAAAAAGAG 420 CCTCAGTCCT CCCCCTTCCC TCCTTCCTTC TCTTGCTTCC TCTTTCACCA TGTGATCTCT 480 GCACAGGTCA GCTCCCCTTT GTCTGCCAGC ATGAGTGGAA GCAACCTGAG GCCCTCAGCA 540 GATGCCTGTT AGGCAGCAGA ATTGTGAACC AAATAGACCT TTTTTCTTTA TAAAGCACCC 600 AGTCTCAGGT GGTGCTTTAT AGCAACACAG AATGGACTAA GACAAAAAGT TAAAATTTAT 660 CAAAACATGC ACAAAACACA CAGATCATAT GTGGTGCAAT TCACAGTTGA GAGAAATGCA 720 AACAAACATA AAGGTACAGT ATTAAACCAC AACTGCAGTA AATGAACTAC AGTACATACT 780 GTATTAAACT GTAATAATTT CATAGCCTCC 810
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