| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:47318723-47319088 | Common:1; Rare:113 | ||||
| chr20:47356664-47356872 | Rare:45 | ||||
| chr20:47501744-47502012 | Common:1; Rare:95 | ||||
| chr20:47786332-47786604 | Common:3; Rare:58 | ||||
| chr20:49219258-49219505 | Common:1; Rare:115 | ||||
| chr20:49278020-49278278 | Rare:69 | ||||
| chr20:49568043-49568152 | Common:1; Rare:27 | ||||
| chr20:49812566-49812888 | Common:2; Rare:71 | ||||
| chr20:50113107-50113244 | Common:5; Rare:68 | ||||
| chr20:50153633-50153866 | Common:2; Rare:94 | ||||
| chr20:50190542-50190833 | Rare:86 | ||||
| chr20:50510219-50510427 | Common:3; Rare:84 | ||||
| chr20:50958438-50958850 | Common:1; Rare:150; Clinvar:4; Clinvar (benign):5 | ||||
| chr20:53593763-53593886 | Common:1; Rare:43 | ||||
| chr20:56392197-56392379 | Rare:45 |