| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:3214587-3214910 | Common:10; Rare:137 | ||||
| chr12:3215074-3215393 | Common:6; Rare:118 | ||||
| chr12:3752252-3753102 | Common:20; Rare:247 | ||||
| chr12:3753032-3753262 | Common:1; Rare:58 | ||||
| chr12:3753168-3753337 | Common:1; Rare:38 | ||||
| chr12:3873060-3873254 | Rare:96 | ||||
| chr12:3873304-3873630 | Common:9; Rare:162 | ||||
| chr12:4307903-4308179 | Common:3; Rare:117 | ||||
| chr12:4320836-4321308 | Common:16; Rare:436 | ||||
| chr12:4538369-4538966 | Common:9; Rare:374 | ||||
| chr12:4648378-4648950 | Common:10; Rare:139 | ||||
| chr12:4648931-4649199 | Common:5; Rare:198; Clinvar (benign):4 | ||||
| chr12:5944640-5944980 | Common:3; Rare:66 | ||||
| chr12:5945168-5945431 | Common:2; Rare:125 | ||||
| chr12:6200003-6200485 | Common:8; Rare:248 |