| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:753886-754127 | Common:1; Rare:95; Clinvar:4; Clinvar (benign):2 | ||||
| chr12:3230908-3231090 | Common:2; Rare:29 | ||||
| chr12:3252463-3252745 | Common:1; Rare:78 | ||||
| chr12:5045233-5045401 | Common:1; Rare:65; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr12:5045684-5045980 | Common:1; Rare:112; Clinvar:8; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr12:5046012-5046068 | Rare:17; Clinvar:1 | ||||
| chr12:6233160-6233486 | Common:1; Rare:71 | ||||
| chr12:7089291-7089712 | Common:3; Rare:135 | ||||
| chr12:8242933-8243244 | Common:8; Rare:88 | ||||
| chr12:9065054-9065186 | Rare:14 | ||||
| chr12:9070486-9070787 | Common:1; Rare:58 | ||||
| chr12:9240327-9240394 | Common:1; Rare:14 | ||||
| chr12:18753642-18753736 | Common:3; Rare:18 | ||||
| chr12:46470144-46470209 | Rare:10 | ||||
| chr12:49565158-49565392 | Common:2; Rare:45 |