| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:213284620-213284774 | Rare:61 | ||||
| chr2:214808962-214809474 | Common:7; Rare:140; Clinvar:10; Clinvar (benign):9 | ||||
| chr2:214809592-214809878 | Common:4; Rare:108; Clinvar:1; Clinvar (benign):4 | ||||
| chr2:214810034-214810320 | Common:9; Rare:79 | ||||
| chr2:215311830-215312184 | Common:8; Rare:134 | ||||
| chr2:216013219-216013380 | Common:1; Rare:53 | ||||
| chr2:216013459-216013660 | Common:2; Rare:41 | ||||
| chr2:216057868-216058140 | Rare:50 | ||||
| chr2:216081658-216081955 | Common:1; Rare:100 | ||||
| chr2:216109024-216109482 | Common:8; Rare:123 | ||||
| chr2:216412261-216412608 | Common:4; Rare:78; Clinvar:2; Clinvar (benign):3 | ||||
| chr2:216412630-216412767 | Rare:16 | ||||
| chr2:216498258-216498359 | Common:3; Rare:16 | ||||
| chr2:216498608-216498961 | Common:11; Rare:129 | ||||
| chr2:217434211-217434387 | Rare:36 |