| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:216497855-216497936 | Rare:23 | ||||
| chr2:216498740-216498886 | Common:5; Rare:60 | ||||
| chr2:216694444-216694845 | Rare:98 | ||||
| chr2:216695536-216695580 | Rare:11 | ||||
| chr2:217901881-217902175 | Common:3; Rare:47 | ||||
| chr2:217905378-217905615 | Rare:47 | ||||
| chr2:218002839-218003106 | Common:2; Rare:70 | ||||
| chr2:218217023-218217254 | Common:1; Rare:79 | ||||
| chr2:218260728-218261038 | Rare:57 | ||||
| chr2:218269995-218270538 | Common:6; Rare:172; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:218287255-218287357 | Rare:18 | ||||
| chr2:218292461-218292626 | Common:1; Rare:47 | ||||
| chr2:218322978-218323291 | Common:6; Rare:103 | ||||
| chr2:218381889-218382350 | Common:3; Rare:92 | ||||
| chr2:218399516-218399776 | Common:1; Rare:117 |