| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:40414812-40415080 | Common:1; Rare:50 | ||||
| chr20:40646552-40646784 | Common:2; Rare:55 | ||||
| chr20:40654969-40655232 | Common:2; Rare:57 | ||||
| chr20:40688535-40688617 | Rare:14; Clinvar (benign):1 | ||||
| chr20:40690029-40690201 | Rare:47 | ||||
| chr20:40991584-40991783 | Rare:26 | ||||
| chr20:41003202-41003530 | Rare:58 | ||||
| chr20:41003556-41003945 | Common:2; Rare:71 | ||||
| chr20:41005407-41005701 | Rare:44 | ||||
| chr20:41007001-41007253 | Common:1; Rare:39 | ||||
| chr20:41029391-41029560 | Rare:68 | ||||
| chr20:41029752-41029867 | Rare:25 | ||||
| chr20:41058397-41058436 | Rare:4 | ||||
| chr20:41058526-41058802 | Rare:48 | ||||
| chr20:41224495-41224631 | Common:1; Rare:19 |