| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:10673942-10674132 | Common:4; Rare:141; Clinvar:6; Clinvar (benign):6 | ||||
| chr20:11890425-11891100 | Common:8; Rare:358 | ||||
| chr20:11891136-11891476 | Common:1; Rare:183 | ||||
| chr20:11892277-11892621 | Common:4; Rare:113 | ||||
| chr20:13638875-13639035 | Common:2; Rare:97 | ||||
| chr20:13784854-13785094 | Common:5; Rare:209; Clinvar:2; Clinvar (benign):6 | ||||
| chr20:13785140-13785570 | Common:7; Rare:256; Clinvar:4; Clinvar (benign):13; Clinvar (pathogenic):1 | ||||
| chr20:15985400-15985930 | Common:7; Rare:148 | ||||
| chr20:16573270-16573730 | Common:3; Rare:214 | ||||
| chr20:16729861-16730063 | Rare:90 | ||||
| chr20:17531270-17531480 | Common:1; Rare:118 | ||||
| chr20:17558730-17559120 | Common:4; Rare:94 | ||||
| chr20:17569170-17569400 | Common:1; Rare:65 | ||||
| chr20:17569893-17570205 | Common:7; Rare:233 | ||||
| chr20:17660260-17660720 | Common:3; Rare:231 |