Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:183185925-183186451 | Common:6; Rare:126; Clinvar:6; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr1:183471974-183472120 | Rare:36 | ||||
chr1:183472281-183472550 | Common:2; Rare:94 | ||||
chr1:183590448-183590576 | Common:2; Rare:19; Clinvar (benign):1 | ||||
chr1:183635068-183635245 | Common:1; Rare:39 | ||||
chr1:183635515-183636109 | Common:5; Rare:173 | ||||
chr1:184051571-184051782 | Common:3; Rare:75 | ||||
chr1:184386766-184387366 | Common:4; Rare:153 | ||||
chr1:184754484-184754537 | Rare:17 | ||||
chr1:184974421-184974693 | Rare:64 | ||||
chr1:185156709-185156745 | Rare:19 | ||||
chr1:185156868-185157313 | Common:2; Rare:127 | ||||
chr1:185305822-185306090 | Common:1; Rare:49 | ||||
chr1:185317010-185317381 | Common:2; Rare:101 | ||||
chr1:186375104-186375551 | Rare:121 |