| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:49278039-49278288 | Rare:70 | ||||
| chr20:49812774-49812925 | Common:2; Rare:43 | ||||
| chr20:49915471-49915822 | Common:4; Rare:105 | ||||
| chr20:49936248-49936410 | Rare:63 | ||||
| chr20:50113112-50113245 | Common:5; Rare:66 | ||||
| chr20:50115941-50116117 | Common:3; Rare:38 | ||||
| chr20:50931212-50931372 | Common:2; Rare:50 | ||||
| chr20:50958481-50958851 | Common:1; Rare:130; Clinvar:1; Clinvar (benign):4 | ||||
| chr20:53593783-53593894 | Common:1; Rare:40 | ||||
| chr20:56392187-56392379 | Rare:47 | ||||
| chr20:56468432-56468695 | Rare:94 | ||||
| chr20:57266094-57266462 | Common:1; Rare:86 | ||||
| chr20:58389013-58389289 | Common:3; Rare:137; Clinvar:4; Clinvar (benign):1 | ||||
| chr20:58651144-58651289 | Common:2; Rare:29; Clinvar (benign):1 | ||||
| chr20:58651597-58651993 | Common:1; Rare:92; Clinvar:1; Clinvar (benign):4 |