| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:209675140-209675446 | Common:2; Rare:75 | ||||
| chr1:209937982-209938262 | Common:3; Rare:96; Clinvar (pathogenic):1 | ||||
| chr1:211259018-211259399 | Common:1; Rare:117 | ||||
| chr1:212035497-212035784 | Common:2; Rare:75 | ||||
| chr1:212791746-212791934 | Common:4; Rare:81 | ||||
| chr1:212858107-212858273 | Common:2; Rare:44; Clinvar:1 | ||||
| chr1:213987699-213987979 | Rare:51 | ||||
| chr1:214280975-214281246 | Common:2; Rare:113 | ||||
| chr1:217631020-217631375 | Common:2; Rare:98 | ||||
| chr1:218285235-218285364 | Rare:64 | ||||
| chr1:219173796-219173900 | Common:1; Rare:58 | ||||
| chr1:220272428-220272572 | Rare:38; Clinvar:1 | ||||
| chr1:222589862-222589965 | Common:2; Rare:28 | ||||
| chr1:222644200-222644392 | Common:1; Rare:53 | ||||
| chr1:222712459-222712854 | Common:3; Rare:141 |