| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:207073716-207073919 | Common:1; Rare:30 | ||||
| chr2:207143807-207144003 | Rare:38 | ||||
| chr2:207311536-207311654 | Rare:17 | ||||
| chr2:207329142-207329307 | Rare:27 | ||||
| chr2:207334695-207334816 | Common:1; Rare:19 | ||||
| chr2:207335280-207335388 | Common:2; Rare:22 | ||||
| chr2:207528693-207529004 | Rare:42 | ||||
| chr2:207530725-207530820 | Rare:25 | ||||
| chr2:207530840-207531215 | Rare:80 | ||||
| chr2:207627204-207627253 | Common:1; Rare:16 | ||||
| chr2:207662232-207662475 | Rare:36 | ||||
| chr2:207724122-207724251 | Rare:25 | ||||
| chr2:207770383-207770469 | Rare:11 | ||||
| chr2:207891489-207891664 | Common:2; Rare:28 | ||||
| chr2:210190367-210190596 | Rare:32 |