| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:46314356-46314624 | Rare:52 | ||||
| chr2:46315101-46315174 | Common:1; Rare:14 | ||||
| chr2:46323803-46324071 | Rare:53 | ||||
| chr2:46327925-46328106 | Common:3; Rare:52 | ||||
| chr2:46332171-46332353 | Common:4; Rare:44 | ||||
| chr2:46346835-46347252 | Common:1; Rare:101; Clinvar:1 | ||||
| chr2:46348086-46348121 | Rare:9 | ||||
| chr2:46378636-46378858 | Common:2; Rare:77; Clinvar:1 | ||||
| chr2:47035013-47035341 | Common:1; Rare:78 | ||||
| chr2:47175169-47175220 | Common:1; Rare:11 | ||||
| chr2:47335095-47335319 | Rare:42 | ||||
| chr2:47795628-47795995 | Common:4; Rare:97; Clinvar:18; Clinvar (benign):11; Clinvar (pathogenic):2 | ||||
| chr2:47803129-47803502 | Common:2; Rare:139; Clinvar:24; Clinvar (benign):16 | ||||
| chr2:47906441-47906819 | Common:2; Rare:143 | ||||
| chr2:49307027-49307227 | Common:2; Rare:51 |