| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:35774619-35775019 | Common:4; Rare:62 | ||||
| chr19:35775179-35775604 | Common:8; Rare:415 | ||||
| chr19:35775587-35775987 | Common:5; Rare:177 | ||||
| chr19:35845380-35845910 | Common:6; Rare:384; Clinvar:20; Clinvar (benign):5; Clinvar (pathogenic):15 | ||||
| chr19:35868310-35868640 | Common:3; Rare:260 | ||||
| chr19:35869724-35869944 | Rare:132 | ||||
| chr19:35869930-35870380 | Common:5; Rare:167 | ||||
| chr19:35899224-35900540 | Common:27; Rare:814 | ||||
| chr19:35900450-35900860 | Common:9; Rare:238 | ||||
| chr19:35902214-35902666 | Common:11; Rare:243 | ||||
| chr19:35994918-35995318 | Common:6; Rare:435; Clinvar:3; Clinvar (benign):4 | ||||
| chr19:35995320-35995550 | Rare:81; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr19:35995645-35996045 | Common:1; Rare:90; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:36014120-36014592 | Common:14; Rare:794 | ||||
| chr19:36054029-36054208 | Rare:130 |