| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:40715035-40715204 | Rare:46 | ||||
| chr19:40716850-40717015 | Common:1; Rare:62 | ||||
| chr19:40750426-40750913 | Common:6; Rare:120 | ||||
| chr19:40751054-40751322 | Common:3; Rare:79 | ||||
| chr19:40751744-40752122 | Common:2; Rare:89 | ||||
| chr19:40777934-40778280 | Common:1; Rare:97 | ||||
| chr19:41193149-41193284 | Common:1; Rare:46 | ||||
| chr19:41262381-41262565 | Rare:32 | ||||
| chr19:41264711-41265138 | Common:2; Rare:94 | ||||
| chr19:41363787-41363983 | Common:1; Rare:71; Clinvar:1 | ||||
| chr19:41364137-41364279 | Rare:44 | ||||
| chr19:41442942-41443200 | Common:1; Rare:45 | ||||
| chr19:41860121-41860285 | Common:1; Rare:67; Clinvar:3; Clinvar (benign):1 | ||||
| chr19:41877016-41877285 | Common:1; Rare:48 | ||||
| chr19:41883016-41883261 | Common:1; Rare:47 |