| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:213050830-213052000 | Common:20; Rare:1006 | ||||
| chr1:213987650-213988010 | Rare:121 | ||||
| chr1:214280478-214281297 | Common:19; Rare:936 | ||||
| chr1:214281322-214281740 | Common:12; Rare:462 | ||||
| chr1:214602860-214603316 | Common:15; Rare:520 | ||||
| chr1:214603461-214603593 | Common:4; Rare:36 | ||||
| chr1:214603633-214604033 | Common:3; Rare:73 | ||||
| chr1:215566825-215567906 | Common:9; Rare:750 | ||||
| chr1:217630990-217631434 | Common:13; Rare:507 | ||||
| chr1:218285115-218285702 | Common:27; Rare:763 | ||||
| chr1:218345425-218346350 | Common:9; Rare:282; Clinvar:15; Clinvar (benign):7 | ||||
| chr1:219173621-219174021 | Common:10; Rare:751 | ||||
| chr1:219174049-219174190 | Rare:27 | ||||
| chr1:219174872-219175272 | Common:1; Rare:76 | ||||
| chr1:219927781-219928451 | Common:1; Rare:518; Clinvar:11 |