| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:39390974-39391436 | Common:1; Rare:179 | ||||
| chr19:39406695-39406946 | Rare:101 | ||||
| chr19:39407081-39407265 | Rare:44 | ||||
| chr19:39445465-39445854 | Common:2; Rare:107 | ||||
| chr19:39480740-39480890 | Common:3; Rare:82; Clinvar (pathogenic):1 | ||||
| chr19:39846294-39846468 | Common:1; Rare:79 | ||||
| chr19:39970948-39971223 | Common:3; Rare:77 | ||||
| chr19:39996956-39997088 | Common:4; Rare:45 | ||||
| chr19:40056135-40056340 | Rare:32 | ||||
| chr19:40090865-40090966 | Common:1; Rare:29 | ||||
| chr19:40285197-40285520 | Common:1; Rare:113 | ||||
| chr19:40348388-40348720 | Common:4; Rare:108 | ||||
| chr19:40425982-40426143 | Common:1; Rare:46 | ||||
| chr19:40444287-40444507 | Common:3; Rare:70 | ||||
| chr19:40601218-40601390 | Rare:54 |