| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:10026243-10026417 | Common:1; Rare:54 | ||||
| chr3:14124739-14125036 | Common:3; Rare:78; Clinvar:2 | ||||
| chr3:14178572-14178857 | Common:2; Rare:147; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:14651502-14651819 | Rare:96 | ||||
| chr3:14947379-14947582 | Common:3; Rare:98 | ||||
| chr3:15427495-15427623 | Rare:47 | ||||
| chr3:15601506-15601781 | Common:4; Rare:113; Clinvar:1 | ||||
| chr3:16264851-16265233 | Common:2; Rare:130 | ||||
| chr3:23916913-23917220 | Rare:116 | ||||
| chr3:29280952-29281076 | Common:2; Rare:19 | ||||
| chr3:37861715-37861911 | Common:1; Rare:43 | ||||
| chr3:38137048-38137447 | Common:1; Rare:96 | ||||
| chr3:39107568-39107705 | Common:3; Rare:43 | ||||
| chr3:39383568-39383660 | Rare:20; Clinvar:1 | ||||
| chr3:42582285-42582428 | Common:1; Rare:37 |