| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:210476686-210476843 | Rare:45 | ||||
| chr2:210477582-210477691 | Rare:38 | ||||
| chr2:213284244-213284490 | Rare:80 | ||||
| chr2:215311883-215312133 | Common:8; Rare:98 | ||||
| chr2:216081761-216081906 | Common:1; Rare:47 | ||||
| chr2:216412694-216412782 | Rare:10 | ||||
| chr2:216498721-216498886 | Common:6; Rare:67 | ||||
| chr2:216694551-216694671 | Rare:29 | ||||
| chr2:217813690-217813960 | Common:1; Rare:70 | ||||
| chr2:217978769-217978934 | Common:1; Rare:47 | ||||
| chr2:218217099-218217215 | Rare:44 | ||||
| chr2:218270028-218270587 | Common:5; Rare:182; Clinvar:5; Clinvar (benign):2 | ||||
| chr2:218292475-218292604 | Rare:33 | ||||
| chr2:218568280-218568649 | Common:3; Rare:99 | ||||
| chr2:218568733-218568957 | Common:1; Rare:63 |