| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:177197747-177197988 | Common:3; Rare:197 | ||||
| chr3:179071572-179071970 | Common:1; Rare:209 | ||||
| chr3:179072130-179072680 | Common:3; Rare:94 | ||||
| chr3:179147860-179148469 | Common:21; Rare:392 | ||||
| chr3:179148790-179149340 | Common:1; Rare:222; Clinvar (benign):1 | ||||
| chr3:179259497-179261028 | Common:16; Rare:433 | ||||
| chr3:179322736-179323125 | Common:12; Rare:274 | ||||
| chr3:179323158-179323601 | Common:6; Rare:246 | ||||
| chr3:179323610-179324040 | Common:7; Rare:186 | ||||
| chr3:179347476-179348009 | Common:5; Rare:220 | ||||
| chr3:179451338-179451611 | Common:3; Rare:211 | ||||
| chr3:179451688-179451818 | Common:1; Rare:35 | ||||
| chr3:179562592-179563090 | Rare:411 | ||||
| chr3:179563446-179563701 | Common:2; Rare:62 | ||||
| chr3:179604551-179604892 | Common:5; Rare:298 |