| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:4303253-4303412 | Common:1; Rare:62 | ||||
| chr3:4493135-4493538 | Common:2; Rare:139; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:4980372-4980538 | Rare:42 | ||||
| chr3:8501653-8501935 | Common:2; Rare:103 | ||||
| chr3:9362978-9363117 | Common:1; Rare:53 | ||||
| chr3:9397434-9397917 | Common:1; Rare:151 | ||||
| chr3:9749797-9750067 | Common:1; Rare:88 | ||||
| chr3:9769875-9770069 | Common:1; Rare:50 | ||||
| chr3:9792384-9792570 | Rare:51 | ||||
| chr3:9792676-9793118 | Common:3; Rare:154 | ||||
| chr3:9916896-9917202 | Common:4; Rare:65 | ||||
| chr3:9933517-9933879 | Common:2; Rare:149; Clinvar:3 | ||||
| chr3:10026295-10026473 | Rare:59 | ||||
| chr3:10141678-10142009 | Common:1; Rare:156; Clinvar:39; Clinvar (benign):34 | ||||
| chr3:10312629-10312915 | Rare:73 |