| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:58909356-58909804 | Rare:97; Clinvar (pathogenic):6 | ||||
| chr20:58909950-58910401 | Rare:104 | ||||
| chr20:59835845-59836027 | Rare:43 | ||||
| chr20:59940283-59940481 | Rare:83 | ||||
| chr20:62143299-62143823 | Common:6; Rare:225 | ||||
| chr20:62182942-62183056 | Rare:33 | ||||
| chr20:62386968-62387377 | Common:3; Rare:146 | ||||
| chr20:62937858-62938205 | Common:2; Rare:127 | ||||
| chr20:63498181-63498451 | Common:5; Rare:63 | ||||
| chr20:63626996-63627282 | Rare:109 | ||||
| chr20:63658204-63658364 | Common:4; Rare:55 | ||||
| chr20:63707850-63708095 | Rare:69 | ||||
| chr20:63865061-63865368 | Common:2; Rare:117 | ||||
| chr20:64079897-64080109 | Common:2; Rare:83 | ||||
| chr21:14383111-14383486 | Common:2; Rare:105 |