| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45891230-45891387 | Common:1; Rare:56; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:45893952-45893993 | Common:1; Rare:14; Clinvar:1 | ||||
| chr20:45896197-45896659 | Common:6; Rare:109 | ||||
| chr20:45935063-45935146 | Rare:34 | ||||
| chr20:46363746-46364067 | Common:1; Rare:61 | ||||
| chr20:46364362-46364551 | Rare:72 | ||||
| chr20:46406565-46406788 | Common:2; Rare:60 | ||||
| chr20:46689389-46689663 | Common:3; Rare:85 | ||||
| chr20:47318712-47319106 | Common:2; Rare:120 | ||||
| chr20:47351716-47351771 | Rare:11 | ||||
| chr20:47356657-47356887 | Rare:54 | ||||
| chr20:47501717-47502121 | Common:1; Rare:132 | ||||
| chr20:48921619-48921879 | Common:2; Rare:113; Clinvar:3; Clinvar (benign):3 | ||||
| chr20:49219258-49219541 | Common:1; Rare:125 | ||||
| chr20:49278031-49278278 | Rare:67 |