| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:241315649-241315978 | Common:5; Rare:128 | ||||
| chr2:241637550-241637704 | Common:1; Rare:81 | ||||
| chr2:241701871-241702062 | Common:1; Rare:78 | ||||
| chr20:844527-844643 | Rare:37 | ||||
| chr20:1118471-1118654 | Common:3; Rare:56 | ||||
| chr20:1325397-1325424 | Rare:6 | ||||
| chr20:1329115-1329308 | Rare:33 | ||||
| chr20:2652434-2652655 | Common:8; Rare:74 | ||||
| chr20:2840672-2840755 | Common:1; Rare:35 | ||||
| chr20:3209439-3209542 | Rare:36 | ||||
| chr20:3846737-3846885 | Rare:44 | ||||
| chr20:5119913-5120155 | Common:1; Rare:83 | ||||
| chr20:5126616-5126863 | Common:3; Rare:70 | ||||
| chr20:5950414-5950656 | Common:8; Rare:72 | ||||
| chr20:13784871-13785080 | Common:2; Rare:93; Clinvar (benign):3 |