| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:3985385-3985590 | Common:1; Rare:123 | ||||
| chr19:4182535-4182692 | Common:1; Rare:57 | ||||
| chr19:4304537-4304716 | Common:3; Rare:57 | ||||
| chr19:4471969-4472328 | Common:6; Rare:132 | ||||
| chr19:4723761-4724068 | Common:7; Rare:118 | ||||
| chr19:5340671-5341074 | Common:2; Rare:160 | ||||
| chr19:5622725-5623201 | Common:5; Rare:189 | ||||
| chr19:5680458-5680772 | Rare:95 | ||||
| chr19:5680872-5681188 | Rare:94 | ||||
| chr19:5903704-5903902 | Common:1; Rare:96; Clinvar:3; Clinvar (benign):3 | ||||
| chr19:5978078-5978395 | Common:3; Rare:119 | ||||
| chr19:6199499-6199831 | Common:13; Rare:105 | ||||
| chr19:6393105-6393227 | Common:2; Rare:29 | ||||
| chr19:6502248-6502395 | Rare:46; Clinvar (benign):1 | ||||
| chr19:7395032-7395185 | Common:4; Rare:47 |