| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31094528-31094820 | Common:1; Rare:110; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr16:31094830-31095070 | Rare:55; Clinvar:1 | ||||
| chr16:31108227-31108528 | Common:1; Rare:59 | ||||
| chr16:31117462-31117696 | Common:2; Rare:68 | ||||
| chr16:31117870-31118102 | Rare:57 | ||||
| chr16:31142170-31142698 | Common:3; Rare:144 | ||||
| chr16:31179666-31180247 | Common:4; Rare:244; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:31180537-31180880 | Common:3; Rare:125 | ||||
| chr16:31202208-31202464 | Common:2; Rare:83 | ||||
| chr16:31202570-31202901 | Common:2; Rare:115 | ||||
| chr16:31202925-31203081 | Rare:40 | ||||
| chr16:31259916-31260038 | Rare:18 | ||||
| chr16:31355035-31355197 | Common:1; Rare:42 | ||||
| chr16:31442726-31443156 | Common:2; Rare:83 | ||||
| chr16:31458167-31458343 | Common:1; Rare:44 |