| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:6381135-6381382 | Common:3; Rare:99 | ||||
| chr19:6393106-6393227 | Common:2; Rare:28 | ||||
| chr19:6416839-6417071 | Common:1; Rare:80 | ||||
| chr19:6464221-6464646 | Common:1; Rare:96 | ||||
| chr19:6468916-6469174 | Common:5; Rare:57 | ||||
| chr19:6739189-6739286 | Common:1; Rare:12 | ||||
| chr19:6740871-6741138 | Rare:76 | ||||
| chr19:6767391-6767755 | Common:4; Rare:73 | ||||
| chr19:7294396-7294542 | Common:1; Rare:37 | ||||
| chr19:7395014-7395215 | Common:6; Rare:60 | ||||
| chr19:7488997-7489123 | Rare:57 | ||||
| chr19:7533858-7534213 | Common:3; Rare:90; Clinvar (benign):1 | ||||
| chr19:7535574-7535759 | Common:3; Rare:65 | ||||
| chr19:7539943-7540208 | Common:1; Rare:65; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:7556959-7557283 | Common:1; Rare:104; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):3 |