| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:216107764-216108036 | Common:2; Rare:51 | ||||
| chr2:216109107-216109429 | Common:7; Rare:93 | ||||
| chr2:216412246-216412564 | Common:3; Rare:76; Clinvar (benign):2 | ||||
| chr2:216412664-216412791 | Rare:15 | ||||
| chr2:216498708-216498921 | Common:8; Rare:98 | ||||
| chr2:216633253-216633445 | Common:1; Rare:69 | ||||
| chr2:216694072-216694253 | Rare:35 | ||||
| chr2:216695519-216695861 | Rare:74 | ||||
| chr2:217433430-217433860 | Common:1; Rare:80 | ||||
| chr2:217434224-217434381 | Rare:30 | ||||
| chr2:217944055-217944203 | Common:1; Rare:29 | ||||
| chr2:218216929-218217203 | Common:2; Rare:86 | ||||
| chr2:218217297-218217868 | Common:5; Rare:220 | ||||
| chr2:218270076-218270435 | Common:5; Rare:113; Clinvar (benign):1 | ||||
| chr2:218322982-218323299 | Common:6; Rare:104 |