| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45791854-45792002 | Common:1; Rare:57 | ||||
| chr20:45857343-45857621 | Common:3; Rare:71 | ||||
| chr20:45891250-45891361 | Common:1; Rare:42; Clinvar:2; Clinvar (benign):1 | ||||
| chr20:45934395-45934716 | Common:2; Rare:135 | ||||
| chr20:45935051-45935406 | Common:1; Rare:142 | ||||
| chr20:45971812-45972073 | Common:3; Rare:75 | ||||
| chr20:45972154-45972211 | Rare:30 | ||||
| chr20:46118717-46118796 | Rare:16 | ||||
| chr20:46363899-46364135 | Common:1; Rare:48 | ||||
| chr20:46406586-46406814 | Common:1; Rare:59 | ||||
| chr20:47356666-47356857 | Rare:42 | ||||
| chr20:47501724-47501974 | Common:1; Rare:88 | ||||
| chr20:47502029-47502121 | Rare:25 | ||||
| chr20:48921569-48921821 | Common:2; Rare:100; Clinvar (benign):1 | ||||
| chr20:49046182-49046337 | Common:2; Rare:42 |