| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:4723747-4724068 | Common:7; Rare:122 | ||||
| chr19:4831693-4831763 | Rare:18 | ||||
| chr19:4867621-4867817 | Common:3; Rare:60 | ||||
| chr19:4909342-4909501 | Common:2; Rare:46 | ||||
| chr19:5293204-5293428 | Common:1; Rare:101 | ||||
| chr19:5622711-5623384 | Common:6; Rare:258 | ||||
| chr19:5680705-5681040 | Rare:79 | ||||
| chr19:5978078-5978383 | Common:3; Rare:113 | ||||
| chr19:6393106-6393238 | Common:2; Rare:32 | ||||
| chr19:6740627-6740939 | Common:1; Rare:70 | ||||
| chr19:7395022-7395185 | Common:4; Rare:50 | ||||
| chr19:7535569-7535769 | Common:3; Rare:71 | ||||
| chr19:7629523-7629858 | Common:5; Rare:119; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7637002-7637143 | Common:2; Rare:48; Clinvar (benign):1 | ||||
| chr19:7920227-7920369 | Rare:62 |