| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:58651131-58651305 | Common:2; Rare:38; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:58651597-58651847 | Common:1; Rare:55; Clinvar:1; Clinvar (benign):2 | ||||
| chr20:58888788-58888999 | Common:1; Rare:63 | ||||
| chr20:58981047-58981312 | Common:3; Rare:128 | ||||
| chr20:62143299-62143748 | Common:5; Rare:188 | ||||
| chr20:62182942-62183049 | Rare:29 | ||||
| chr20:62386953-62387129 | Common:3; Rare:76 | ||||
| chr20:62937883-62938193 | Common:2; Rare:114 | ||||
| chr20:63254433-63254767 | Common:1; Rare:105 | ||||
| chr20:63272712-63272858 | Common:4; Rare:47 | ||||
| chr20:63520649-63520784 | Common:2; Rare:63 | ||||
| chr20:63626976-63627243 | Rare:104 | ||||
| chr20:63653407-63653669 | Common:2; Rare:31 | ||||
| chr20:63707875-63708118 | Rare:71 | ||||
| chr20:63865027-63865340 | Common:2; Rare:107 |