| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:197499815-197500430 | Common:1; Rare:238; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:197515873-197516101 | Common:1; Rare:88 | ||||
| chr2:197705124-197705396 | Common:3; Rare:114 | ||||
| chr2:200306405-200306562 | Common:2; Rare:35 | ||||
| chr2:200509896-200510024 | Common:1; Rare:44 | ||||
| chr2:200510040-200510134 | Rare:31 | ||||
| chr2:200811324-200811614 | Common:1; Rare:95 | ||||
| chr2:200864585-200864784 | Common:1; Rare:74 | ||||
| chr2:200888965-200889440 | Common:3; Rare:151 | ||||
| chr2:200963447-200963535 | Rare:16 | ||||
| chr2:200963588-200963715 | Common:1; Rare:35 | ||||
| chr2:201071598-201072047 | Rare:98 | ||||
| chr2:201115893-201116202 | Common:2; Rare:57 | ||||
| chr2:201116400-201116454 | Rare:10 | ||||
| chr2:201117344-201117596 | Rare:32 |