| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:151346560-151347130 | Rare:292; Clinvar:1 | ||||
| chr1:151347131-151347583 | Rare:253 | ||||
| chr1:151399373-151399796 | Common:11; Rare:296; Clinvar (pathogenic):5 | ||||
| chr1:151458274-151458995 | Common:10; Rare:570 | ||||
| chr1:151459076-151459614 | Common:8; Rare:454 | ||||
| chr1:151510630-151511009 | Common:3; Rare:91 | ||||
| chr1:151511058-151511522 | Common:14; Rare:268 | ||||
| chr1:151539461-151539933 | Common:2; Rare:59 | ||||
| chr1:151540013-151540428 | Common:4; Rare:288 | ||||
| chr1:151540433-151540638 | Rare:48 | ||||
| chr1:151611945-151612868 | Common:4; Rare:584; Clinvar:5; Clinvar (benign):8 | ||||
| chr1:151716701-151717101 | Common:3; Rare:285 | ||||
| chr1:151763180-151763726 | Common:8; Rare:423 | ||||
| chr1:151790385-151790906 | Common:9; Rare:363 | ||||
| chr1:151831279-151832151 | Common:14; Rare:495; Clinvar:5; Clinvar (benign):5 |