| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:2004415-2004672 | Common:2; Rare:86 | ||||
| chr12:2795027-2795208 | Rare:74 | ||||
| chr12:2796956-2797170 | Rare:54 | ||||
| chr12:2812339-2812728 | Common:1; Rare:93 | ||||
| chr12:2812884-2813057 | Rare:48 | ||||
| chr12:2877006-2877253 | Rare:73 | ||||
| chr12:3873355-3873514 | Common:1; Rare:36 | ||||
| chr12:4273543-4274191 | Common:2; Rare:186; Clinvar (benign):1 | ||||
| chr12:4275444-4275578 | Common:2; Rare:18 | ||||
| chr12:4320969-4321253 | Common:5; Rare:105 | ||||
| chr12:4538444-4538942 | Common:3; Rare:113 | ||||
| chr12:4648994-4649149 | Common:2; Rare:51; Clinvar (benign):1 | ||||
| chr12:6200005-6200480 | Common:4; Rare:138 | ||||
| chr12:6493193-6493502 | Common:8; Rare:90 | ||||
| chr12:6493776-6494140 | Common:2; Rare:108 |