| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:41860081-41860293 | Common:1; Rare:85; Clinvar:3; Clinvar (benign):1 | ||||
| chr19:41860756-41861411 | Common:5; Rare:336; Clinvar:7; Clinvar (benign):11; Clinvar (pathogenic):5 | ||||
| chr19:41884121-41884369 | Rare:58 | ||||
| chr19:41959277-41959462 | Common:1; Rare:60 | ||||
| chr19:41994178-41994344 | Common:1; Rare:43; Clinvar:2 | ||||
| chr19:41997934-41998099 | Rare:25 | ||||
| chr19:42066010-42066410 | Common:2; Rare:130 | ||||
| chr19:42069645-42070146 | Common:1; Rare:182 | ||||
| chr19:42075745-42076223 | Common:5; Rare:140 | ||||
| chr19:42217671-42217904 | Rare:89 | ||||
| chr19:42220021-42220485 | Common:3; Rare:124 | ||||
| chr19:42242549-42242863 | Common:1; Rare:92 | ||||
| chr19:42243098-42243411 | Common:3; Rare:110 | ||||
| chr19:42253250-42254219 | Common:8; Rare:527 | ||||
| chr19:42255116-42255281 | Common:1; Rare:61 |