| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:40286930-40287310 | Common:2; Rare:79 | ||||
| chr20:40317495-40317895 | Common:4; Rare:151 | ||||
| chr20:40397590-40397937 | Common:3; Rare:53 | ||||
| chr20:40619099-40620047 | Common:13; Rare:346 | ||||
| chr20:40648107-40649016 | Common:1; Rare:309 | ||||
| chr20:40649280-40649690 | Common:7; Rare:71 | ||||
| chr20:40673350-40673780 | Common:2; Rare:83 | ||||
| chr20:40687629-40687805 | Rare:33; Clinvar:1; Clinvar (benign):2 | ||||
| chr20:40687767-40688057 | Rare:80; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:40689989-40690321 | Rare:129 | ||||
| chr20:40958637-40958927 | Rare:59 | ||||
| chr20:40962683-40962903 | Common:1; Rare:38 | ||||
| chr20:41003120-41003910 | Common:2; Rare:245 | ||||
| chr20:41017650-41018190 | Common:10; Rare:145 | ||||
| chr20:41029712-41029943 | Rare:59 |