| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:2841248-2841520 | Common:2; Rare:83 | ||||
| chr19:2900669-2900966 | Common:9; Rare:115 | ||||
| chr19:2944917-2945234 | Common:7; Rare:107 | ||||
| chr19:3971040-3971377 | Common:2; Rare:117 | ||||
| chr19:4007434-4007760 | Common:3; Rare:120 | ||||
| chr19:4474736-4474885 | Common:1; Rare:33 | ||||
| chr19:4867658-4867859 | Common:2; Rare:58 | ||||
| chr19:5293213-5293433 | Common:1; Rare:99 | ||||
| chr19:5622756-5623188 | Common:5; Rare:164 | ||||
| chr19:5680904-5681173 | Rare:84 | ||||
| chr19:5978082-5978393 | Common:3; Rare:116 | ||||
| chr19:6740842-6740939 | Rare:19 | ||||
| chr19:7395039-7395185 | Common:4; Rare:47 | ||||
| chr19:7489006-7489164 | Common:2; Rare:71 | ||||
| chr19:7629531-7629859 | Common:5; Rare:115; Clinvar (benign):2; Clinvar (pathogenic):1 |