| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:46160296-46160464 | Common:1; Rare:50 | ||||
| chr19:46346941-46347105 | Common:3; Rare:52 | ||||
| chr19:46600978-46601409 | Common:4; Rare:147; Clinvar (benign):1 | ||||
| chr19:46715798-46716063 | Common:2; Rare:43 | ||||
| chr19:46745885-46746061 | Common:3; Rare:38 | ||||
| chr19:46746290-46746595 | Common:4; Rare:87 | ||||
| chr19:46788548-46788604 | Rare:14 | ||||
| chr19:47094530-47094740 | Rare:52 | ||||
| chr19:47113097-47113429 | Common:2; Rare:88 | ||||
| chr19:47256472-47256604 | Rare:48 | ||||
| chr19:47608113-47608183 | Rare:20 | ||||
| chr19:47778400-47778551 | Common:2; Rare:38 | ||||
| chr19:47778567-47778833 | Common:3; Rare:113 | ||||
| chr19:48170266-48170705 | Common:2; Rare:119 | ||||
| chr19:48321160-48321524 | Common:3; Rare:98 |