| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:61017120-61017330 | Common:6; Rare:69 | ||||
| chr2:61017383-61017774 | Common:2; Rare:238; Clinvar:6; Clinvar (benign):4 | ||||
| chr2:61144890-61145199 | Common:6; Rare:194 | ||||
| chr2:61177120-61177580 | Common:13; Rare:330 | ||||
| chr2:61185212-61185900 | Common:5; Rare:374 | ||||
| chr2:61470645-61471037 | Common:2; Rare:252 | ||||
| chr2:61471164-61471390 | Common:5; Rare:163 | ||||
| chr2:61536501-61536773 | Common:3; Rare:152 | ||||
| chr2:61537921-61538604 | Common:8; Rare:257 | ||||
| chr2:61538591-61539060 | Common:1; Rare:166 | ||||
| chr2:61854410-61854950 | Common:3; Rare:166 | ||||
| chr2:61876770-61877250 | Common:1; Rare:115 | ||||
| chr2:61888405-61888757 | Common:4; Rare:289 | ||||
| chr2:62195463-62196202 | Common:9; Rare:363 | ||||
| chr2:62705250-62705979 | Common:2; Rare:224 |