| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:47356688-47356896 | Rare:53 | ||||
| chr20:49046204-49046341 | Common:2; Rare:38 | ||||
| chr20:49278037-49278236 | Rare:54 | ||||
| chr20:49567926-49568072 | Common:2; Rare:39 | ||||
| chr20:49915481-49915570 | Common:2; Rare:34 | ||||
| chr20:50958476-50958843 | Common:1; Rare:128; Clinvar:1; Clinvar (benign):4 | ||||
| chr20:56392197-56392545 | Common:3; Rare:95 | ||||
| chr20:57709919-57710200 | Rare:80 | ||||
| chr20:58515382-58515533 | Common:2; Rare:29 | ||||
| chr20:58908932-58909423 | Common:4; Rare:114; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr20:59032283-59032568 | Common:2; Rare:116; Clinvar (benign):3 | ||||
| chr20:62143374-62143792 | Common:4; Rare:168 | ||||
| chr20:62182962-62183049 | Rare:19 | ||||
| chr20:62387022-62387124 | Common:2; Rare:44 | ||||
| chr20:62804566-62804850 | Common:2; Rare:74 |