| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:3379611-3379720 | Common:1; Rare:32 | ||||
| chr2:3519495-3519636 | Common:2; Rare:43 | ||||
| chr2:3558269-3558658 | Common:6; Rare:138 | ||||
| chr2:3575114-3575358 | Common:2; Rare:71; Clinvar:3; Clinvar (benign):5 | ||||
| chr2:9423163-9423276 | Common:1; Rare:26 | ||||
| chr2:9423443-9423676 | Rare:73 | ||||
| chr2:9474526-9474630 | Common:6; Rare:48 | ||||
| chr2:9555765-9555992 | Common:1; Rare:76 | ||||
| chr2:10689925-10690004 | Common:2; Rare:25 | ||||
| chr2:10812704-10812996 | Common:3; Rare:110 | ||||
| chr2:11466143-11466286 | Common:3; Rare:32 | ||||
| chr2:12716660-12716963 | Common:1; Rare:92 | ||||
| chr2:17753759-17754168 | Common:4; Rare:130; Clinvar (benign):1 | ||||
| chr2:19901685-19901987 | Common:2; Rare:115 | ||||
| chr2:19990076-19990211 | Rare:34 |