| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:214551538-214552125 | Common:3; Rare:166 | ||||
| chr1:214552373-214552579 | Common:2; Rare:36 | ||||
| chr1:214602874-214603398 | Common:4; Rare:142 | ||||
| chr1:214603470-214603585 | Common:2; Rare:19 | ||||
| chr1:214603667-214603747 | Rare:12 | ||||
| chr1:215567042-215567198 | Common:2; Rare:39 | ||||
| chr1:215567296-215567451 | Rare:47 | ||||
| chr1:215567827-215567946 | Rare:26 | ||||
| chr1:217630980-217631453 | Common:5; Rare:140 | ||||
| chr1:218285059-218285356 | Common:4; Rare:112 | ||||
| chr1:218285556-218285601 | Common:1; Rare:7 | ||||
| chr1:218345917-218346017 | Common:1; Rare:29; Clinvar:1; Clinvar (benign):1 | ||||
| chr1:218346145-218346312 | Rare:26 | ||||
| chr1:219173741-219173941 | Common:2; Rare:110 | ||||
| chr1:219174110-219174191 | Rare:13 |