| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:3366463-3366655 | Common:3; Rare:53 | ||||
| chr19:3572655-3573006 | Common:1; Rare:97 | ||||
| chr19:3606862-3606920 | Rare:15 | ||||
| chr19:3982805-3983292 | Common:5; Rare:175; Clinvar:1; Clinvar (benign):6 | ||||
| chr19:4007443-4007766 | Common:3; Rare:118 | ||||
| chr19:4182495-4182692 | Common:1; Rare:76; Clinvar:1 | ||||
| chr19:4540068-4540379 | Rare:68 | ||||
| chr19:4723747-4723865 | Common:1; Rare:40 | ||||
| chr19:4831657-4831770 | Common:1; Rare:34 | ||||
| chr19:4867618-4867855 | Common:3; Rare:72 | ||||
| chr19:5293168-5293425 | Common:1; Rare:108 | ||||
| chr19:5622674-5623284 | Common:6; Rare:250 | ||||
| chr19:5680468-5681169 | Rare:207 | ||||
| chr19:5978069-5978373 | Common:3; Rare:114 | ||||
| chr19:6110416-6110811 | Common:2; Rare:116 |