| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:113214410-113214609 | Common:3; Rare:31 | ||||
| chr4:118279110-118279196 | Common:3; Rare:24 | ||||
| chr4:118591553-118591868 | Common:4; Rare:104 | ||||
| chr4:118939205-118939348 | Common:2; Rare:27 | ||||
| chr4:118976478-118976484 | Rare:2 | ||||
| chr4:119027815-119028043 | Common:1; Rare:39 | ||||
| chr4:119029733-119029889 | Common:2; Rare:31 | ||||
| chr4:119454561-119454904 | Common:16; Rare:117 | ||||
| chr4:119567100-119567318 | Rare:42 | ||||
| chr4:125314854-125315199 | Common:4; Rare:90 | ||||
| chr4:139762872-139763081 | Common:3; Rare:29 | ||||
| chr4:153788332-153788563 | Rare:82 | ||||
| chr4:168915767-168915952 | Common:1; Rare:44; Clinvar:1; Clinvar (benign):2 | ||||
| chr4:168924139-168924418 | Rare:67; Clinvar:4; Clinvar (benign):1 | ||||
| chr4:173509569-173509675 | Common:1; Rare:26 |