| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:49046156-49046368 | Common:3; Rare:67 | ||||
| chr20:49278031-49278301 | Rare:73 | ||||
| chr20:49568045-49568157 | Common:2; Rare:27 | ||||
| chr20:49915496-49915585 | Common:3; Rare:26 | ||||
| chr20:50113106-50113343 | Common:6; Rare:88 | ||||
| chr20:50153604-50153909 | Common:3; Rare:118 | ||||
| chr20:50190538-50190833 | Rare:87 | ||||
| chr20:50958471-50958860 | Common:1; Rare:142; Clinvar:1; Clinvar (benign):4 | ||||
| chr20:51562773-51563051 | Common:3; Rare:57 | ||||
| chr20:53593775-53593894 | Common:1; Rare:42 | ||||
| chr20:56392203-56392541 | Common:3; Rare:92 | ||||
| chr20:58388987-58389281 | Common:3; Rare:136; Clinvar:4; Clinvar (benign):1 | ||||
| chr20:58651135-58651305 | Common:2; Rare:37; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:58888839-58889117 | Common:1; Rare:80 | ||||
| chr20:59006410-59006631 | Rare:72 |