| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:170870163-170870312 | Rare:76 | ||||
| chr3:170908570-170908787 | Common:1; Rare:58 | ||||
| chr3:172039278-172039656 | Common:2; Rare:93 | ||||
| chr3:172040232-172040613 | Common:3; Rare:92 | ||||
| chr3:172750348-172750787 | Common:4; Rare:98 | ||||
| chr3:172750949-172751026 | Rare:23 | ||||
| chr3:174440881-174440987 | Common:2; Rare:30 | ||||
| chr3:179071553-179071908 | Rare:101 | ||||
| chr3:179347630-179347792 | Common:1; Rare:43 | ||||
| chr3:179562668-179563003 | Rare:109 | ||||
| chr3:179604620-179604872 | Common:2; Rare:98 | ||||
| chr3:180601960-180602239 | Common:1; Rare:86 | ||||
| chr3:180912557-180912713 | Common:1; Rare:57 | ||||
| chr3:180989640-180989782 | Rare:63; Clinvar:1 | ||||
| chr3:183099443-183099758 | Common:2; Rare:100; Clinvar:3; Clinvar (benign):5 |