| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:38515486-38515711 | Common:3; Rare:54 | ||||
| chr2:38535079-38535237 | Common:1; Rare:43 | ||||
| chr2:38995273-38995515 | Rare:51; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:42053112-42053289 | Common:2; Rare:43; Clinvar (pathogenic):1 | ||||
| chr2:42810502-42810536 | Common:1; Rare:23 | ||||
| chr2:42811123-42811340 | Rare:64 | ||||
| chr2:47790749-47791092 | Common:2; Rare:89; Clinvar:19; Clinvar (benign):17; Clinvar (pathogenic):1 | ||||
| chr2:47906479-47906815 | Common:2; Rare:120 | ||||
| chr2:48515585-48515726 | Rare:31 | ||||
| chr2:55282289-55282362 | Common:4; Rare:25 | ||||
| chr2:55322662-55322920 | Common:1; Rare:58 | ||||
| chr2:66575265-66575462 | Common:8; Rare:52 | ||||
| chr2:66581593-66581917 | Common:6; Rare:84 | ||||
| chr2:66582911-66583042 | Common:2; Rare:18 | ||||
| chr2:70086252-70086520 | Common:4; Rare:117 |