| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:212285064-212285463 | Common:3; Rare:128 | ||||
| chr1:212432768-212433116 | Rare:93 | ||||
| chr1:212608522-212608792 | Rare:70 | ||||
| chr1:212791756-212791964 | Common:4; Rare:94 | ||||
| chr1:212858093-212858318 | Common:4; Rare:60; Clinvar:2 | ||||
| chr1:213015434-213015586 | Rare:40 | ||||
| chr1:213015742-213015915 | Rare:43 | ||||
| chr1:214551580-214551881 | Common:2; Rare:108 | ||||
| chr1:214602920-214603324 | Common:4; Rare:111 | ||||
| chr1:215567310-215567794 | Common:1; Rare:154 | ||||
| chr1:217631006-217631385 | Common:3; Rare:112 | ||||
| chr1:218285185-218285456 | Common:4; Rare:115 | ||||
| chr1:218345676-218346100 | Common:6; Rare:114; Clinvar:9; Clinvar (benign):5 | ||||
| chr1:218346111-218346460 | Rare:59; Clinvar:1; Clinvar (benign):2 | ||||
| chr1:218346471-218346845 | Common:1; Rare:90; Clinvar:2; Clinvar (benign):6 |