| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9792414-9792621 | Rare:52 | ||||
| chr3:10026356-10026480 | Rare:32 | ||||
| chr3:11225904-11225991 | Rare:11 | ||||
| chr3:12664089-12664351 | Common:1; Rare:77; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:14124728-14125100 | Common:4; Rare:106; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178559-14178858 | Common:2; Rare:157; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14651486-14651781 | Rare:77 | ||||
| chr3:15427498-15427618 | Rare:44 | ||||
| chr3:16264899-16265209 | Common:2; Rare:95 | ||||
| chr3:23916973-23917173 | Rare:68 | ||||
| chr3:36993209-36993525 | Common:2; Rare:90; Clinvar:21; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr3:42581932-42582074 | Common:2; Rare:43 | ||||
| chr3:42804443-42804603 | Common:2; Rare:47 | ||||
| chr3:44761613-44761774 | Common:2; Rare:56 | ||||
| chr3:44861803-44861915 | Common:2; Rare:54 |