| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:216108852-216109574 | Common:13; Rare:199 | ||||
| chr2:216412018-216412943 | Common:8; Rare:249; Clinvar:3; Clinvar (benign):5 | ||||
| chr2:216498719-216498908 | Common:12; Rare:154 | ||||
| chr2:218217021-218217285 | Common:3; Rare:161 | ||||
| chr2:218270095-218270557 | Common:10; Rare:245; Clinvar:4; Clinvar (benign):2 | ||||
| chr2:218322982-218323310 | Common:6; Rare:109 | ||||
| chr2:218398094-218398245 | Common:2; Rare:99 | ||||
| chr2:218398480-218398740 | Common:6; Rare:160 | ||||
| chr2:218399662-218400077 | Rare:179 | ||||
| chr2:218568141-218568967 | Common:12; Rare:373 | ||||
| chr2:218659326-218659801 | Common:4; Rare:180 | ||||
| chr2:218671954-218672327 | Common:2; Rare:137 | ||||
| chr2:219160360-219160650 | Common:6; Rare:82 | ||||
| chr2:219160783-219160935 | Common:2; Rare:85 | ||||
| chr2:219176829-219177098 | Common:7; Rare:143 |