| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:85708319-85708488 | Common:2; Rare:53 | ||||
| chr1:86704535-86704966 | Common:3; Rare:157 | ||||
| chr1:86914297-86914852 | Common:3; Rare:161 | ||||
| chr1:87328764-87329239 | Common:4; Rare:144 | ||||
| chr1:88684106-88684451 | Common:2; Rare:84 | ||||
| chr1:88684962-88685112 | Rare:43 | ||||
| chr1:88832842-88832869 | Rare:5 | ||||
| chr1:88992588-88992977 | Common:3; Rare:100 | ||||
| chr1:89065195-89065252 | Rare:13 | ||||
| chr1:89524771-89524950 | Common:1; Rare:75 | ||||
| chr1:89632900-89633207 | Common:1; Rare:88 | ||||
| chr1:89821736-89822027 | Rare:78 | ||||
| chr1:89994977-89995250 | Common:2; Rare:106 | ||||
| chr1:92298927-92299073 | Common:1; Rare:69; Clinvar:2; Clinvar (benign):1 | ||||
| chr1:92831891-92832156 | Common:1; Rare:119; Clinvar:7; Clinvar (benign):7 |