| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38596022-38596356 | Rare:90 | ||||
| chr19:38618787-38619259 | Common:4; Rare:136 | ||||
| chr19:38619329-38619335 | Rare:2 | ||||
| chr19:38647332-38647788 | Common:3; Rare:150 | ||||
| chr19:38736099-38736148 | Rare:18 | ||||
| chr19:38736176-38736307 | Common:3; Rare:69 | ||||
| chr19:38736785-38737235 | Common:8; Rare:108 | ||||
| chr19:38737470-38737608 | Common:2; Rare:70 | ||||
| chr19:38831127-38831522 | Common:3; Rare:164; Clinvar (benign):1 | ||||
| chr19:38831706-38832077 | Common:5; Rare:122; Clinvar (benign):1 | ||||
| chr19:38837647-38837845 | Rare:63 | ||||
| chr19:38839498-38839560 | Rare:25 | ||||
| chr19:38849209-38849679 | Common:2; Rare:178 | ||||
| chr19:38849766-38850238 | Common:3; Rare:172 | ||||
| chr19:38850346-38850840 | Common:2; Rare:159 |