| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:15099122-15099299 | Rare:43 | ||||
| chr3:15206069-15206274 | Rare:80 | ||||
| chr3:15427470-15427623 | Common:1; Rare:57 | ||||
| chr3:15601485-15601823 | Common:5; Rare:141; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:15859544-15859684 | Common:2; Rare:41 | ||||
| chr3:15859800-15860086 | Common:4; Rare:89 | ||||
| chr3:16264874-16265243 | Common:2; Rare:122 | ||||
| chr3:16670298-16670481 | Common:1; Rare:22 | ||||
| chr3:17742596-17742956 | Common:4; Rare:126 | ||||
| chr3:19946974-19947437 | Common:7; Rare:172 | ||||
| chr3:20186166-20186415 | Common:2; Rare:79 | ||||
| chr3:21751106-21751236 | Common:1; Rare:47 | ||||
| chr3:23805826-23806066 | Common:1; Rare:49 | ||||
| chr3:23916890-23917214 | Rare:124 | ||||
| chr3:25783371-25783647 | Common:2; Rare:93; Clinvar (benign):3 |