| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:68252141-68252264 | Common:2; Rare:41 | ||||
| chr2:68252486-68252863 | Common:3; Rare:118 | ||||
| chr2:68319360-68319592 | Common:1; Rare:77 | ||||
| chr2:68319765-68319820 | Rare:10 | ||||
| chr2:68319927-68320059 | Rare:32 | ||||
| chr2:68467253-68467622 | Common:2; Rare:100 | ||||
| chr2:69387119-69387398 | Rare:78; Clinvar:2 | ||||
| chr2:69437428-69437549 | Rare:56; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:69643598-69643834 | Rare:82 | ||||
| chr2:69829477-69829741 | Common:1; Rare:107 | ||||
| chr2:69893866-69894004 | Rare:38 | ||||
| chr2:70087414-70087768 | Rare:138 | ||||
| chr2:70190990-70191124 | Rare:31 | ||||
| chr2:70257978-70258182 | Common:1; Rare:73 | ||||
| chr2:70293665-70293848 | Common:2; Rare:60 |