| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:179562554-179563089 | Rare:818 | ||||
| chr3:179563033-179563433 | Rare:221 | ||||
| chr3:179586570-179586970 | Common:1; Rare:79 | ||||
| chr3:179604157-179604557 | Rare:91 | ||||
| chr3:179604564-179604909 | Common:16; Rare:748 | ||||
| chr3:179652278-179653200 | Common:8; Rare:244 | ||||
| chr3:179653326-179653726 | Common:6; Rare:123 | ||||
| chr3:180601556-180601956 | Common:3; Rare:80 | ||||
| chr3:180601925-180602342 | Common:8; Rare:604 | ||||
| chr3:180602352-180602752 | Common:2; Rare:142 | ||||
| chr3:180868549-180868949 | Common:2; Rare:80 | ||||
| chr3:180869810-180870522 | Common:9; Rare:205 | ||||
| chr3:180912207-180912754 | Common:13; Rare:529 | ||||
| chr3:180989560-180990040 | Rare:704; Clinvar:8; Clinvar (benign):5 | ||||
| chr3:182793124-182794029 | Common:26; Rare:823 |