| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:44531691-44531774 | Common:1; Rare:20 | ||||
| chr20:44531790-44531982 | Common:1; Rare:60 | ||||
| chr20:44651634-44651822 | Common:1; Rare:56; Clinvar (benign):1 | ||||
| chr20:44885460-44885842 | Common:6; Rare:119 | ||||
| chr20:44960345-44960514 | Common:1; Rare:70 | ||||
| chr20:45363127-45363208 | Rare:28 | ||||
| chr20:45416035-45416153 | Rare:30 | ||||
| chr20:45791848-45791989 | Rare:49 | ||||
| chr20:45857339-45857632 | Common:3; Rare:77 | ||||
| chr20:45891250-45891390 | Common:1; Rare:51; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:45910863-45911184 | Common:4; Rare:86 | ||||
| chr20:45971831-45972025 | Common:1; Rare:56 | ||||
| chr20:46363668-46364008 | Common:1; Rare:71 | ||||
| chr20:46364356-46364561 | Common:1; Rare:77 | ||||
| chr20:47356666-47356887 | Rare:51 |