| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:130002818-130002967 | Common:1; Rare:30 | ||||
| chr11:130069581-130069990 | Common:2; Rare:153 | ||||
| chr11:130314429-130314520 | Common:1; Rare:26 | ||||
| chr11:130916426-130916663 | Common:5; Rare:71 | ||||
| chr11:134253273-134253586 | Common:2; Rare:105; Clinvar (benign):1 | ||||
| chr12:389249-389347 | Rare:38 | ||||
| chr12:401446-401687 | Rare:66 | ||||
| chr12:2004408-2004692 | Common:2; Rare:97 | ||||
| chr12:2812891-2813057 | Rare:44 | ||||
| chr12:2877027-2877262 | Rare:70 | ||||
| chr12:3077240-3077423 | Common:6; Rare:80 | ||||
| chr12:3873306-3873527 | Common:4; Rare:47 | ||||
| chr12:4320942-4321266 | Common:5; Rare:125 | ||||
| chr12:4509296-4509455 | Common:1; Rare:34 | ||||
| chr12:4538449-4538940 | Common:3; Rare:111 |