| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:4457710-4457959 | Common:13; Rare:101 | ||||
| chr19:4472001-4472380 | Common:5; Rare:148 | ||||
| chr19:4525823-4525922 | Common:6; Rare:46 | ||||
| chr19:4723747-4724068 | Common:7; Rare:122 | ||||
| chr19:4831663-4832044 | Common:3; Rare:81 | ||||
| chr19:4867617-4867810 | Common:3; Rare:59 | ||||
| chr19:5622669-5623324 | Common:6; Rare:263 | ||||
| chr19:5680927-5681169 | Rare:78 | ||||
| chr19:5978069-5978418 | Common:3; Rare:134 | ||||
| chr19:6393119-6393480 | Common:4; Rare:93 | ||||
| chr19:7395022-7395203 | Common:4; Rare:58 | ||||
| chr19:7488993-7489078 | Rare:40 | ||||
| chr19:7535631-7535747 | Common:2; Rare:34 | ||||
| chr19:7629531-7629848 | Common:5; Rare:113; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7636953-7637143 | Common:2; Rare:59; Clinvar (benign):1 |