| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:2004420-2004669 | Common:2; Rare:80 | ||||
| chr12:2812638-2812727 | Rare:33 | ||||
| chr12:2812885-2812966 | Rare:30 | ||||
| chr12:2877027-2877262 | Rare:70 | ||||
| chr12:2959821-2959901 | Rare:20 | ||||
| chr12:3753107-3753245 | Rare:36 | ||||
| chr12:3873355-3873581 | Common:2; Rare:53 | ||||
| chr12:4320949-4321266 | Common:5; Rare:122 | ||||
| chr12:4538436-4538933 | Common:3; Rare:113 | ||||
| chr12:4648994-4649165 | Common:2; Rare:57; Clinvar (benign):2 | ||||
| chr12:6200013-6200480 | Common:4; Rare:132 | ||||
| chr12:6341912-6342194 | Rare:53; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:6384005-6384250 | Common:1; Rare:51 | ||||
| chr12:6386101-6386380 | Common:1; Rare:70 | ||||
| chr12:6493230-6493502 | Common:7; Rare:81 |