| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9792364-9792604 | Rare:68 | ||||
| chr3:9792726-9793136 | Common:3; Rare:144 | ||||
| chr3:9843986-9844136 | Common:2; Rare:55 | ||||
| chr3:9917042-9917137 | Common:1; Rare:19 | ||||
| chr3:9933557-9933857 | Common:2; Rare:116; Clinvar:2 | ||||
| chr3:10026304-10026489 | Rare:57 | ||||
| chr3:11154338-11154528 | Common:4; Rare:52 | ||||
| chr3:12664053-12664337 | Common:2; Rare:81; Clinvar:1; Clinvar (benign):4 | ||||
| chr3:14124713-14125099 | Common:4; Rare:115; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178569-14178876 | Common:2; Rare:158; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14651468-14651813 | Rare:101 | ||||
| chr3:14947283-14947583 | Common:3; Rare:134 | ||||
| chr3:15427478-15427623 | Common:1; Rare:51 | ||||
| chr3:15601512-15601756 | Common:4; Rare:100 | ||||
| chr3:16264881-16265239 | Common:2; Rare:117 |