| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:3846724-3846893 | Rare:50 | ||||
| chr20:3889157-3889397 | Common:1; Rare:124; Clinvar:5; Clinvar (benign):2 | ||||
| chr20:4686212-4686471 | Common:1; Rare:60; Clinvar (benign):1 | ||||
| chr20:5112866-5113168 | Common:1; Rare:114 | ||||
| chr20:5119922-5120149 | Common:1; Rare:77 | ||||
| chr20:5610904-5611208 | Common:2; Rare:111 | ||||
| chr20:5950315-5950689 | Common:8; Rare:112 | ||||
| chr20:13784882-13785049 | Common:2; Rare:67; Clinvar (benign):1 | ||||
| chr20:17569949-17570124 | Common:2; Rare:70 | ||||
| chr20:17968755-17969130 | Common:4; Rare:136 | ||||
| chr20:18467162-18467453 | Common:1; Rare:55 | ||||
| chr20:18507457-18507624 | Rare:42; Clinvar:1 | ||||
| chr20:18567231-18567586 | Common:4; Rare:118 | ||||
| chr20:20017242-20017396 | Rare:56 | ||||
| chr20:21303700-21303860 | Rare:48 |