| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:134253298-134253586 | Common:2; Rare:94; Clinvar (benign):1 | ||||
| chr12:389249-389364 | Rare:40 | ||||
| chr12:401446-401660 | Rare:56 | ||||
| chr12:2004373-2004677 | Common:2; Rare:109 | ||||
| chr12:2812638-2812713 | Rare:26 | ||||
| chr12:2877027-2877262 | Rare:70 | ||||
| chr12:3077289-3077438 | Common:5; Rare:66 | ||||
| chr12:3753064-3753236 | Common:1; Rare:42 | ||||
| chr12:3873355-3873535 | Common:1; Rare:40 | ||||
| chr12:4320943-4321273 | Common:5; Rare:128 | ||||
| chr12:4538440-4538934 | Common:3; Rare:111 | ||||
| chr12:4649016-4649154 | Common:2; Rare:49; Clinvar (benign):1 | ||||
| chr12:6124532-6124764 | Rare:31; Clinvar:1 | ||||
| chr12:6200012-6200559 | Common:4; Rare:161 | ||||
| chr12:6383976-6384297 | Common:2; Rare:76 |