| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:40310210-40310530 | Common:2; Rare:83; Clinvar:4; Clinvar (pathogenic):2 | ||||
| chr12:40326254-40326663 | Common:8; Rare:192 | ||||
| chr12:40332820-40333593 | Common:12; Rare:237 | ||||
| chr12:40698153-40698337 | Common:2; Rare:25 | ||||
| chr12:41061189-41061953 | Common:1; Rare:228 | ||||
| chr12:41143014-41143414 | Common:5; Rare:110 | ||||
| chr12:41932531-41932709 | Common:3; Rare:51 | ||||
| chr12:42012530-42013000 | Common:4; Rare:79 | ||||
| chr12:42865190-42866153 | Common:33; Rare:325 | ||||
| chr12:43470957-43471384 | Common:12; Rare:292 | ||||
| chr12:43586544-43586944 | Common:11; Rare:142 | ||||
| chr12:43675280-43675650 | Common:5; Rare:49 | ||||
| chr12:44686822-44687010 | Common:3; Rare:49 | ||||
| chr12:44835380-44835850 | Common:3; Rare:80 | ||||
| chr12:44948714-44949040 | Common:3; Rare:91 |