| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:217901881-217902156 | Common:3; Rare:47 | ||||
| chr2:217905409-217905594 | Rare:35 | ||||
| chr2:217943871-217943902 | Rare:7 | ||||
| chr2:218002947-218003309 | Common:9; Rare:73 | ||||
| chr2:218217057-218217262 | Common:1; Rare:70 | ||||
| chr2:218260743-218261043 | Rare:58 | ||||
| chr2:218270054-218270559 | Common:5; Rare:159; Clinvar:4; Clinvar (benign):1 | ||||
| chr2:218285652-218285859 | Common:1; Rare:32 | ||||
| chr2:218285888-218286070 | Rare:32 | ||||
| chr2:218287249-218287427 | Common:1; Rare:30 | ||||
| chr2:218289974-218290229 | Common:3; Rare:39 | ||||
| chr2:218316606-218316753 | Common:1; Rare:16 | ||||
| chr2:218322982-218323310 | Common:6; Rare:109 | ||||
| chr2:218381906-218382375 | Common:2; Rare:93 | ||||
| chr2:218568182-218568702 | Common:6; Rare:130 |