| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:154241527-154241753 | Common:2; Rare:40 | ||||
| chr3:154255109-154255267 | Common:2; Rare:33 | ||||
| chr3:155737774-155738096 | Common:1; Rare:42 | ||||
| chr3:156816952-156817363 | Common:1; Rare:121 | ||||
| chr3:157174851-157175223 | Common:3; Rare:159 | ||||
| chr3:157272466-157272776 | Common:2; Rare:53 | ||||
| chr3:158730563-158730820 | Common:3; Rare:51 | ||||
| chr3:159763077-159763147 | Rare:17 | ||||
| chr3:169764892-169765222 | Common:1; Rare:122; Clinvar:12; Clinvar (pathogenic):5 | ||||
| chr3:170097358-170097422 | Rare:17 | ||||
| chr3:179358654-179358946 | Rare:74 | ||||
| chr3:183132262-183132494 | Common:3; Rare:44 | ||||
| chr3:184322700-184322948 | Rare:63 | ||||
| chr3:185418803-185419109 | Common:1; Rare:44 | ||||
| chr3:187740273-187740296 | Rare:3 |