| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:841219-841297 | Common:2; Rare:21 | ||||
| chr20:1002309-1002410 | Rare:29 | ||||
| chr20:1118408-1118681 | Common:4; Rare:91 | ||||
| chr20:1313603-1313730 | Rare:34 | ||||
| chr20:1325239-1325426 | Rare:45 | ||||
| chr20:1392876-1393250 | Common:2; Rare:141 | ||||
| chr20:2102329-2102696 | Common:1; Rare:111 | ||||
| chr20:2470692-2470997 | Common:4; Rare:108 | ||||
| chr20:2652415-2652684 | Common:8; Rare:111 | ||||
| chr20:2652823-2653302 | Common:4; Rare:164; Clinvar (benign):1 | ||||
| chr20:2654188-2654870 | Common:5; Rare:225; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:2656397-2656949 | Common:3; Rare:199; Clinvar (benign):1 | ||||
| chr20:2659511-2659772 | Rare:98; Clinvar:3 | ||||
| chr20:2663730-2663817 | Common:1; Rare:41; Clinvar (benign):1 | ||||
| chr20:2664151-2664284 | Common:3; Rare:58; Clinvar:1 |