| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45834008-45834240 | Rare:199 | ||||
| chr20:45857243-45857727 | Common:11; Rare:325 | ||||
| chr20:45881000-45881307 | Common:6; Rare:183 | ||||
| chr20:45891177-45891443 | Common:3; Rare:210; Clinvar:9; Clinvar (benign):3 | ||||
| chr20:45910903-45911220 | Common:8; Rare:173 | ||||
| chr20:45934361-45934985 | Common:10; Rare:523 | ||||
| chr20:45934934-45935442 | Common:4; Rare:516 | ||||
| chr20:45971498-45972073 | Common:8; Rare:282 | ||||
| chr20:45972097-45972682 | Common:5; Rare:515 | ||||
| chr20:46021630-46021763 | Common:2; Rare:40 | ||||
| chr20:46021833-46022307 | Common:6; Rare:236 | ||||
| chr20:46089575-46089761 | Common:3; Rare:73 | ||||
| chr20:46089791-46090054 | Rare:149 | ||||
| chr20:46363260-46364203 | Common:3; Rare:333 | ||||
| chr20:46364187-46364583 | Common:7; Rare:261 |