| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:235128744-235128962 | Rare:92 | ||||
| chr1:235328127-235328636 | Common:4; Rare:160 | ||||
| chr1:235866856-235867144 | Common:3; Rare:88 | ||||
| chr1:236064931-236064963 | Rare:9 | ||||
| chr1:236065037-236065353 | Common:3; Rare:119; Clinvar (pathogenic):1 | ||||
| chr1:236281943-236282233 | Common:6; Rare:82 | ||||
| chr1:236523508-236523740 | Common:3; Rare:55 | ||||
| chr1:236523833-236524060 | Common:3; Rare:59 | ||||
| chr1:236524497-236524608 | Common:1; Rare:29 | ||||
| chr1:236540411-236540639 | Common:5; Rare:76 | ||||
| chr1:236604481-236604631 | Common:4; Rare:41 | ||||
| chr1:236686327-236686505 | Rare:77 | ||||
| chr1:236795086-236795480 | Common:5; Rare:164; Clinvar:4 | ||||
| chr1:237042132-237042572 | Common:3; Rare:139; Clinvar:5; Clinvar (benign):6 | ||||
| chr1:241519656-241519977 | Common:2; Rare:105; Clinvar:12; Clinvar (benign):10; Clinvar (pathogenic):4 |