| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:150363628-150363794 | Common:2; Rare:65 | ||||
| chr1:150365375-150365794 | Common:7; Rare:118 | ||||
| chr1:150515482-150515782 | Common:1; Rare:174 | ||||
| chr1:150516236-150516740 | Common:5; Rare:91 | ||||
| chr1:150560159-150560726 | Common:2; Rare:184; Clinvar:9; Clinvar (benign):2 | ||||
| chr1:150560836-150561275 | Common:1; Rare:117; Clinvar:2; Clinvar (benign):1 | ||||
| chr1:150561200-150561608 | Common:4; Rare:334 | ||||
| chr1:150562032-150562444 | Common:3; Rare:199 | ||||
| chr1:150562749-150563123 | Common:2; Rare:103 | ||||
| chr1:150563558-150563887 | Common:3; Rare:45 | ||||
| chr1:150564061-150564511 | Rare:89 | ||||
| chr1:150564618-150565764 | Common:6; Rare:205 | ||||
| chr1:150567318-150567851 | Common:9; Rare:220 | ||||
| chr1:150567923-150568353 | Rare:148 | ||||
| chr1:150572820-150573220 | Common:3; Rare:196 |