| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:200811324-200811596 | Common:1; Rare:87 | ||||
| chr2:200888989-200889451 | Common:3; Rare:144 | ||||
| chr2:200963622-200963838 | Common:1; Rare:56 | ||||
| chr2:201071626-201072052 | Rare:87 | ||||
| chr2:201118367-201118792 | Rare:66 | ||||
| chr2:201257971-201258099 | Common:1; Rare:22 | ||||
| chr2:201451444-201451838 | Common:2; Rare:101 | ||||
| chr2:201642637-201642773 | Rare:68 | ||||
| chr2:201643435-201643553 | Rare:36; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:201780890-201781243 | Common:3; Rare:108; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:202238498-202238621 | Rare:40 | ||||
| chr2:202871648-202871711 | Rare:20 | ||||
| chr2:202911606-202911740 | Rare:23 | ||||
| chr2:202911881-202912024 | Rare:30 | ||||
| chr2:202912127-202912298 | Common:2; Rare:57 |