| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:169764892-169765252 | Common:1; Rare:128; Clinvar:12; Clinvar (pathogenic):5 | ||||
| chr3:170097371-170097433 | Rare:20 | ||||
| chr3:171709640-171709989 | Common:3; Rare:74 | ||||
| chr3:177300453-177300617 | Rare:32 | ||||
| chr3:183447431-183447674 | Common:2; Rare:62 | ||||
| chr3:184015622-184015832 | Rare:26 | ||||
| chr3:184352155-184352335 | Rare:56; Clinvar:2 | ||||
| chr3:185379233-185379297 | Common:2; Rare:14 | ||||
| chr3:185465624-185465816 | Common:2; Rare:45 | ||||
| chr3:188263948-188264222 | Rare:44 | ||||
| chr3:194131342-194131380 | Rare:8 | ||||
| chr3:194583866-194584027 | Common:11; Rare:56 | ||||
| chr3:195616248-195616486 | Common:3; Rare:17 | ||||
| chr3:195683810-195684148 | Common:4; Rare:54 | ||||
| chr3:195710637-195710715 | Common:5; Rare:11 |