| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:210315224-210315527 | Common:3; Rare:73 | ||||
| chr2:210477580-210477690 | Rare:38 | ||||
| chr2:212538537-212538893 | Common:1; Rare:108 | ||||
| chr2:212538969-212539185 | Common:1; Rare:47 | ||||
| chr2:212539223-212539457 | Common:6; Rare:43 | ||||
| chr2:213284238-213284490 | Rare:82 | ||||
| chr2:215311888-215312139 | Common:8; Rare:98 | ||||
| chr2:215435654-215435820 | Common:2; Rare:47 | ||||
| chr2:215435849-215435944 | Rare:13 | ||||
| chr2:215435962-215436241 | Common:2; Rare:88 | ||||
| chr2:216081737-216081955 | Common:1; Rare:72 | ||||
| chr2:216412217-216412561 | Common:3; Rare:80; Clinvar (benign):2 | ||||
| chr2:216412667-216412781 | Rare:13 | ||||
| chr2:216498732-216498886 | Common:5; Rare:65 | ||||
| chr2:216694462-216694659 | Rare:44 |