| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:134331705-134331995 | Common:10; Rare:60 | ||||
| chr12:389256-389360 | Rare:35 | ||||
| chr12:2004435-2004474 | Rare:16 | ||||
| chr12:2812638-2812727 | Rare:33 | ||||
| chr12:2877031-2877253 | Rare:67 | ||||
| chr12:4274170-4274232 | Rare:7 | ||||
| chr12:4275455-4275670 | Common:2; Rare:32 | ||||
| chr12:4320947-4321236 | Common:4; Rare:105 | ||||
| chr12:4538436-4538579 | Rare:34 | ||||
| chr12:4538715-4538914 | Common:2; Rare:41 | ||||
| chr12:4649010-4649144 | Common:2; Rare:43; Clinvar (benign):1 | ||||
| chr12:6199838-6200004 | Common:1; Rare:33 | ||||
| chr12:6200031-6200448 | Common:4; Rare:115 | ||||
| chr12:6493184-6493365 | Common:7; Rare:48 | ||||
| chr12:6493760-6494126 | Common:2; Rare:107 |