| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:11374889-11375236 | Common:1; Rare:108 | ||||
| chr19:11381172-11381445 | Common:2; Rare:164; Clinvar:1 | ||||
| chr19:11381500-11381950 | Common:1; Rare:159; Clinvar (benign):3 | ||||
| chr19:11418540-11418920 | Common:1; Rare:113 | ||||
| chr19:11419280-11419449 | Common:1; Rare:65 | ||||
| chr19:11435094-11435441 | Common:4; Rare:146 | ||||
| chr19:11435513-11435741 | Common:6; Rare:168; Clinvar:4; Clinvar (benign):6 | ||||
| chr19:11442101-11442620 | Common:4; Rare:175; Clinvar (benign):3 | ||||
| chr19:11446832-11447743 | Common:17; Rare:443; Clinvar:9; Clinvar (benign):11 | ||||
| chr19:11505060-11505450 | Common:4; Rare:254 | ||||
| chr19:11505722-11505981 | Common:2; Rare:212 | ||||
| chr19:11529048-11529309 | Common:1; Rare:93 | ||||
| chr19:11559186-11559464 | Common:5; Rare:155 | ||||
| chr19:11597283-11597520 | Common:1; Rare:131 | ||||
| chr19:11738840-11739250 | Common:8; Rare:210 |