| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45972147-45972536 | Common:1; Rare:139 | ||||
| chr20:46021849-46022226 | Common:3; Rare:97 | ||||
| chr20:46118155-46118330 | Common:2; Rare:65; Clinvar:2; Clinvar (benign):2 | ||||
| chr20:46364049-46364070 | Rare:4 | ||||
| chr20:46364322-46364526 | Common:1; Rare:75 | ||||
| chr20:46406546-46406788 | Common:2; Rare:68 | ||||
| chr20:46513451-46513680 | Common:3; Rare:82 | ||||
| chr20:46689399-46689751 | Common:2; Rare:97 | ||||
| chr20:47318966-47319144 | Common:1; Rare:56 | ||||
| chr20:47319146-47319219 | Rare:20 | ||||
| chr20:47319458-47319661 | Common:2; Rare:27 | ||||
| chr20:47501720-47502015 | Common:1; Rare:103 | ||||
| chr20:47786535-47786738 | Common:5; Rare:30 | ||||
| chr20:48921516-48921797 | Common:3; Rare:106; Clinvar (benign):1 | ||||
| chr20:49046166-49046401 | Common:3; Rare:73 |