| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:42423526-42423813 | Common:4; Rare:94 | ||||
| chr19:42423990-42424284 | Common:1; Rare:69 | ||||
| chr19:42528433-42528604 | Common:2; Rare:40 | ||||
| chr19:43527169-43527310 | Common:5; Rare:55; Clinvar:3; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr19:43533423-43533455 | Rare:9 | ||||
| chr19:43575448-43575852 | Common:3; Rare:106 | ||||
| chr19:43595997-43596433 | Common:4; Rare:138 | ||||
| chr19:43619472-43619547 | Rare:16 | ||||
| chr19:43619572-43619686 | Common:1; Rare:33 | ||||
| chr19:43670111-43670306 | Common:2; Rare:48 | ||||
| chr19:43754850-43755107 | Common:3; Rare:102 | ||||
| chr19:43901755-43901888 | Common:2; Rare:27 | ||||
| chr19:43935231-43935366 | Common:2; Rare:37 | ||||
| chr19:44002759-44003013 | Common:6; Rare:65 | ||||
| chr19:44072047-44072181 | Common:1; Rare:33 |