| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49660973-49661038 | Rare:14 | ||||
| chr19:49665350-49665450 | Rare:26 | ||||
| chr19:49665561-49666075 | Common:6; Rare:231; Clinvar (pathogenic):1 | ||||
| chr19:49677144-49677313 | Common:1; Rare:64 | ||||
| chr19:49804753-49805086 | Common:2; Rare:62 | ||||
| chr19:49850776-49851037 | Common:1; Rare:91 | ||||
| chr19:49851053-49851184 | Common:1; Rare:52 | ||||
| chr19:49856293-49856414 | Common:2; Rare:28 | ||||
| chr19:49856870-49857128 | Rare:125; Clinvar (benign):1 | ||||
| chr19:49857670-49857978 | Common:2; Rare:138 | ||||
| chr19:49858211-49858578 | Common:3; Rare:117 | ||||
| chr19:49859986-49860447 | Common:3; Rare:195 | ||||
| chr19:49876199-49876260 | Rare:25 | ||||
| chr19:49876582-49876681 | Rare:34 | ||||
| chr19:49877200-49877726 | Common:2; Rare:132 |