| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:11197466-11197794 | Common:3; Rare:199 | ||||
| chr19:11197760-11198110 | Common:4; Rare:225 | ||||
| chr19:11262356-11262563 | Common:3; Rare:158 | ||||
| chr19:11339468-11339856 | Common:13; Rare:221 | ||||
| chr19:11344321-11344741 | Common:3; Rare:110 | ||||
| chr19:11344960-11345372 | Common:4; Rare:183 | ||||
| chr19:11346011-11346831 | Rare:458 | ||||
| chr19:11355497-11356755 | Common:12; Rare:303 | ||||
| chr19:11374509-11374775 | Common:2; Rare:169 | ||||
| chr19:11374830-11375288 | Common:5; Rare:410 | ||||
| chr19:11381090-11381491 | Common:5; Rare:305; Clinvar:2; Clinvar (benign):1 | ||||
| chr19:11381522-11381885 | Common:1; Rare:219; Clinvar (benign):5 | ||||
| chr19:11384222-11384851 | Common:15; Rare:339; Clinvar:3; Clinvar (benign):3 | ||||
| chr19:11418446-11419051 | Common:1; Rare:181 | ||||
| chr19:11435098-11436427 | Common:25; Rare:865; Clinvar:8; Clinvar (benign):17 |