| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:41262313-41262598 | Rare:50 | ||||
| chr19:41310058-41310298 | Rare:93 | ||||
| chr19:41363743-41363992 | Common:1; Rare:78; Clinvar:1 | ||||
| chr19:41364100-41364332 | Common:1; Rare:71; Clinvar:1 | ||||
| chr19:41376691-41376782 | Rare:34 | ||||
| chr19:41397321-41397839 | Common:11; Rare:157; Clinvar (benign):4 | ||||
| chr19:41439535-41439686 | Common:1; Rare:40 | ||||
| chr19:41884132-41884443 | Rare:75 | ||||
| chr19:41959272-41959459 | Common:1; Rare:61 | ||||
| chr19:41994150-41994341 | Common:1; Rare:49; Clinvar:2 | ||||
| chr19:42070159-42070302 | Rare:36 | ||||
| chr19:42075765-42076209 | Common:5; Rare:131 | ||||
| chr19:42217696-42217874 | Rare:66 | ||||
| chr19:42220128-42220354 | Common:2; Rare:62 | ||||
| chr19:42302278-42302831 | Common:3; Rare:138 |