Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:185282838-185283003 | Common:1; Rare:45 | ||||
chr3:185498967-185499155 | Rare:66 | ||||
chr3:186567291-186567426 | Common:3; Rare:35 | ||||
chr3:193593109-193593267 | Rare:47 | ||||
chr3:197791220-197791270 | Rare:24 | ||||
chr3:197949894-197950266 | Common:4; Rare:113; Clinvar (benign):2 | ||||
chr3:197959994-197960242 | Common:1; Rare:88 | ||||
chr4:499149-499281 | Common:2; Rare:40 | ||||
chr4:674253-674552 | Common:1; Rare:138 | ||||
chr4:932264-932465 | Common:2; Rare:80 | ||||
chr4:1113508-1113627 | Common:2; Rare:43 | ||||
chr4:1289650-1289906 | Common:1; Rare:84 | ||||
chr4:2468871-2469159 | Common:3; Rare:101 | ||||
chr4:2843687-2843957 | Common:2; Rare:98 | ||||
chr4:4290117-4290259 | Common:3; Rare:53 |