| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:111898242-111898656 | Common:2; Rare:109 | ||||
| chr2:112255012-112255193 | Common:2; Rare:80 | ||||
| chr2:112275384-112275637 | Common:1; Rare:89 | ||||
| chr2:112542105-112542493 | Common:1; Rare:121 | ||||
| chr2:112584355-112584639 | Common:1; Rare:78 | ||||
| chr2:112584772-112584951 | Rare:40 | ||||
| chr2:112645707-112645951 | Common:1; Rare:92 | ||||
| chr2:112646261-112646378 | Common:1; Rare:41 | ||||
| chr2:112764591-112764815 | Common:2; Rare:74; Clinvar (pathogenic):1 | ||||
| chr2:113127355-113127622 | Rare:55 | ||||
| chr2:113236904-113236951 | Common:1; Rare:2 | ||||
| chr2:113236954-113236989 | Rare:7 | ||||
| chr2:113237079-113237118 | Rare:6 | ||||
| chr2:113241779-113241941 | Rare:33 | ||||
| chr2:113437634-113437884 | Common:4; Rare:98 |