| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:63574210-63574312 | Rare:26 | ||||
| chr20:63626971-63627278 | Rare:121 | ||||
| chr20:63658258-63658380 | Common:2; Rare:46 | ||||
| chr20:63707868-63708141 | Rare:83 | ||||
| chr20:63740954-63741297 | Common:1; Rare:96 | ||||
| chr20:63865031-63865385 | Common:2; Rare:127 | ||||
| chr20:63956368-63956656 | Common:1; Rare:110 | ||||
| chr20:63969847-63970095 | Common:3; Rare:87 | ||||
| chr20:63980985-63981313 | Common:4; Rare:105; Clinvar:7; Clinvar (benign):5 | ||||
| chr20:64079788-64080082 | Common:1; Rare:103 | ||||
| chr21:5128350-5128578 | Rare:50 | ||||
| chr21:14383103-14383522 | Common:3; Rare:117 | ||||
| chr21:17512467-17512615 | Common:2; Rare:39 | ||||
| chr21:17512912-17513138 | Common:1; Rare:83 | ||||
| chr21:17612779-17613056 | Common:1; Rare:121 |