| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:172465434-172465609 | Rare:49 | ||||
| chr2:172475347-172475656 | Common:4; Rare:69 | ||||
| chr2:172479711-172480052 | Common:3; Rare:78; Clinvar (benign):1 | ||||
| chr2:172480968-172481151 | Rare:29 | ||||
| chr2:172497740-172498100 | Common:1; Rare:71; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:172503403-172503689 | Common:3; Rare:41 | ||||
| chr2:172925863-172926062 | Common:1; Rare:29 | ||||
| chr2:172928894-172928941 | Rare:2 | ||||
| chr2:173190904-173191177 | Common:2; Rare:56; Clinvar (pathogenic):1 | ||||
| chr2:173941067-173941118 | Rare:6 | ||||
| chr2:173947464-173947760 | Common:2; Rare:62 | ||||
| chr2:174221250-174221491 | Common:5; Rare:37 | ||||
| chr2:174221798-174221891 | Common:1; Rare:11 | ||||
| chr2:174221902-174222050 | Common:1; Rare:20 | ||||
| chr2:174309826-174310195 | Common:2; Rare:59 |