Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:30946903-30947156 | Rare:54 | ||||
chr16:35506086-35506287 | Common:1; Rare:54 | ||||
chr16:35506457-35506529 | Rare:14 | ||||
chr16:53373380-53373508 | Rare:30 | ||||
chr16:70042935-70042977 | Rare:3 | ||||
chr16:70065766-70065963 | Common:1; Rare:69 | ||||
chr16:72664968-72665187 | Rare:73 | ||||
chr16:74305049-74305538 | Rare:139 | ||||
chr16:74368127-74368338 | Common:1; Rare:62 | ||||
chr16:79598895-79598977 | Rare:20; Clinvar (benign):1 | ||||
chr16:79770410-79770470 | Common:1; Rare:16 | ||||
chr16:88722650-88722851 | Common:3; Rare:101 | ||||
chr16:88734503-88734726 | Common:3; Rare:110; Clinvar (benign):1 | ||||
chr17:1676037-1676273 | Rare:48; Clinvar (benign):1 | ||||
chr17:3386287-3386382 | Common:2; Rare:34 |