| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:37671625-37671776 | Common:2; Rare:68 | ||||
| chr2:38751245-38751628 | Common:6; Rare:201 | ||||
| chr2:38875853-38876059 | Common:2; Rare:73 | ||||
| chr2:39437077-39437456 | Common:4; Rare:137 | ||||
| chr2:42169171-42169399 | Common:1; Rare:122 | ||||
| chr2:42567916-42568213 | Rare:74 | ||||
| chr2:42792538-42792834 | Common:3; Rare:85 | ||||
| chr2:43595931-43596200 | Common:1; Rare:95 | ||||
| chr2:43637086-43637371 | Common:2; Rare:92 | ||||
| chr2:44361473-44362023 | Common:4; Rare:175 | ||||
| chr2:46616972-46617255 | Common:6; Rare:118 | ||||
| chr2:46699009-46699331 | Common:1; Rare:96 | ||||
| chr2:46915733-46915895 | Common:1; Rare:43; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:47369151-47369314 | Common:1; Rare:67; Clinvar:5; Clinvar (benign):2 | ||||
| chr2:47402956-47403330 | Common:1; Rare:180; Clinvar:71; Clinvar (benign):48; Clinvar (pathogenic):4 |