Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:104041302-104041499 | Common:1; Rare:62; Clinvar:2; Clinvar (benign):1 | ||||
chr10:114320764-114321025 | Common:5; Rare:65 | ||||
chr10:119682527-119682688 | Common:1; Rare:22 | ||||
chr10:125691456-125691544 | Rare:28 | ||||
chr11:840434-840605 | Common:5; Rare:66 | ||||
chr11:2933462-2933730 | Rare:69 | ||||
chr11:7906252-7906458 | Common:3; Rare:31 | ||||
chr11:9364384-9364634 | Common:3; Rare:62 | ||||
chr11:9758145-9758307 | Rare:44 | ||||
chr11:12076088-12076283 | Common:2; Rare:34 | ||||
chr11:12086342-12086604 | Common:2; Rare:45 | ||||
chr11:12086702-12086878 | Common:2; Rare:29 | ||||
chr11:12693618-12693915 | Rare:53 | ||||
chr11:27202127-27202244 | Common:1; Rare:22 | ||||
chr11:57778585-57778840 | Rare:43 |