| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:39433367-39433737 | Common:1; Rare:118 | ||||
| chr19:39435854-39436154 | Common:6; Rare:107 | ||||
| chr19:39480639-39480931 | Common:3; Rare:152; Clinvar (pathogenic):1 | ||||
| chr19:39540108-39540342 | Common:2; Rare:60 | ||||
| chr19:39846308-39846468 | Common:1; Rare:75 | ||||
| chr19:39970891-39971213 | Common:5; Rare:93 | ||||
| chr19:39996925-39997128 | Common:5; Rare:64 | ||||
| chr19:40056147-40056270 | Rare:16 | ||||
| chr19:40090847-40091006 | Common:1; Rare:44 | ||||
| chr19:40285197-40285623 | Common:3; Rare:141 | ||||
| chr19:40348347-40348760 | Common:4; Rare:132 | ||||
| chr19:40366395-40366678 | Rare:77 | ||||
| chr19:40377792-40378206 | Common:2; Rare:145; Clinvar (benign):1 | ||||
| chr19:40425964-40426143 | Common:1; Rare:58 | ||||
| chr19:40444233-40444519 | Common:3; Rare:92 |