| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:216498732-216499055 | Common:12; Rare:124 | ||||
| chr2:216694359-216694475 | Rare:31 | ||||
| chr2:218216866-218217239 | Common:2; Rare:110 | ||||
| chr2:218270084-218270557 | Common:5; Rare:150; Clinvar:4; Clinvar (benign):1 | ||||
| chr2:218568023-218568107 | Rare:21 | ||||
| chr2:218568213-218568659 | Common:5; Rare:115 | ||||
| chr2:218568788-218568967 | Common:1; Rare:57 | ||||
| chr2:218659322-218659777 | Common:4; Rare:115 | ||||
| chr2:218671936-218672372 | Common:2; Rare:126 | ||||
| chr2:218710709-218711011 | Common:2; Rare:71 | ||||
| chr2:219160772-219160879 | Common:1; Rare:38 | ||||
| chr2:219176827-219177142 | Common:4; Rare:91 | ||||
| chr2:219178107-219178469 | Common:6; Rare:147 | ||||
| chr2:219206649-219206946 | Rare:101 | ||||
| chr2:219229330-219229375 | Rare:13 |