| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:46689416-46689657 | Common:1; Rare:66 | ||||
| chr20:47318310-47318658 | Rare:87 | ||||
| chr20:47318731-47318813 | Rare:24 | ||||
| chr20:47318993-47319106 | Common:1; Rare:29 | ||||
| chr20:47356661-47356888 | Rare:53 | ||||
| chr20:48921604-48921850 | Common:2; Rare:101; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:49219303-49219541 | Rare:110 | ||||
| chr20:49278036-49278245 | Rare:57 | ||||
| chr20:49812560-49812937 | Common:3; Rare:89 | ||||
| chr20:49915481-49915553 | Rare:30 | ||||
| chr20:50113112-50113244 | Common:5; Rare:65 | ||||
| chr20:50153641-50153925 | Common:2; Rare:113 | ||||
| chr20:50691480-50691759 | Rare:41 | ||||
| chr20:50958490-50958853 | Common:1; Rare:125; Clinvar:1; Clinvar (benign):3 | ||||
| chr20:51562835-51563064 | Common:1; Rare:37 |