| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:12556810-12557150 | Common:5; Rare:101 | ||||
| chr3:13480036-13480339 | Common:2; Rare:71 | ||||
| chr3:14124742-14125179 | Common:4; Rare:127; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178569-14178881 | Common:2; Rare:161; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14651486-14651817 | Rare:97 | ||||
| chr3:14947131-14947557 | Common:5; Rare:183 | ||||
| chr3:14948017-14948211 | Rare:86 | ||||
| chr3:15427465-15427630 | Common:1; Rare:59 | ||||
| chr3:15601502-15601804 | Common:4; Rare:125; Clinvar:1 | ||||
| chr3:15859800-15860057 | Common:4; Rare:83 | ||||
| chr3:16264866-16265229 | Common:2; Rare:121 | ||||
| chr3:16513497-16513775 | Common:4; Rare:66 | ||||
| chr3:19946974-19947457 | Common:7; Rare:179 | ||||
| chr3:20186176-20186500 | Common:3; Rare:102 | ||||
| chr3:23916911-23917177 | Rare:99 |