| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:169764989-169765268 | Common:1; Rare:105; Clinvar:7; Clinvar (pathogenic):3 | ||||
| chr3:170726663-170726878 | Rare:38 | ||||
| chr3:170802493-170802690 | Common:1; Rare:36 | ||||
| chr3:172153416-172153524 | Rare:15 | ||||
| chr3:172749371-172749542 | Rare:28 | ||||
| chr3:183285947-183286078 | Common:3; Rare:25 | ||||
| chr3:183447469-183447682 | Common:1; Rare:55 | ||||
| chr3:184183991-184184196 | Common:2; Rare:41 | ||||
| chr3:185658612-185658861 | Common:1; Rare:51 | ||||
| chr3:185702912-185703114 | Common:1; Rare:31 | ||||
| chr3:186283828-186283966 | Rare:30 | ||||
| chr3:188266108-188266293 | Rare:37 | ||||
| chr3:194583851-194584027 | Common:11; Rare:63 | ||||
| chr3:195657934-195658110 | Common:10; Rare:30 | ||||
| chr3:195900730-195901018 | Common:1; Rare:61 |