| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:35936263-35936399 | Rare:30 | ||||
| chr19:35936309-35936409 | Rare:17 | ||||
| chr19:36127867-36128132 | Common:12; Rare:92 | ||||
| chr19:38700430-38700960 | Common:5; Rare:193; Clinvar (benign):2 | ||||
| chr19:39402599-39402900 | Rare:109 | ||||
| chr19:39403614-39404228 | Common:1; Rare:216 | ||||
| chr19:39409555-39409955 | Common:2; Rare:157 | ||||
| chr19:39430551-39431100 | Common:9; Rare:219 | ||||
| chr19:39453130-39453700 | Common:4; Rare:249 | ||||
| chr19:40190810-40191130 | Rare:121 | ||||
| chr19:40374251-40374580 | Rare:170; Clinvar:2 | ||||
| chr19:40404250-40404560 | Common:3; Rare:95 | ||||
| chr19:40420820-40421545 | Common:11; Rare:314 | ||||
| chr19:40433808-40434156 | Common:2; Rare:173 | ||||
| chr19:40605102-40605511 | Common:2; Rare:230; Clinvar:3; Clinvar (benign):4 |