| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:205321741-205321942 | Common:1; Rare:70 | ||||
| chr1:205632009-205632081 | Common:2; Rare:29 | ||||
| chr1:205750146-205750410 | Common:3; Rare:64 | ||||
| chr1:205813125-205813436 | Common:3; Rare:128 | ||||
| chr1:206612331-206612661 | Common:5; Rare:97 | ||||
| chr1:207050950-207051142 | Common:1; Rare:83 | ||||
| chr1:207052957-207053275 | Common:1; Rare:80 | ||||
| chr1:207751844-207752225 | Common:2; Rare:128; Clinvar:1 | ||||
| chr1:208244255-208244540 | Common:1; Rare:84 | ||||
| chr1:209784468-209784755 | Common:1; Rare:96 | ||||
| chr1:209827769-209828090 | Common:3; Rare:85 | ||||
| chr1:209937952-209938267 | Common:3; Rare:108; Clinvar (pathogenic):1 | ||||
| chr1:210328815-210328922 | Common:1; Rare:39 | ||||
| chr1:210329247-210329316 | Rare:25 | ||||
| chr1:211258936-211259400 | Common:3; Rare:169 |