| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:55729647-55729801 | Rare:33 | ||||
| chr12:55829501-55829820 | Rare:102 | ||||
| chr12:55830002-55830161 | Rare:32 | ||||
| chr12:55830525-55830612 | Common:1; Rare:20 | ||||
| chr12:55830739-55830889 | Rare:57 | ||||
| chr12:55927730-55928003 | Rare:76 | ||||
| chr12:55932002-55932107 | Rare:24 | ||||
| chr12:55966700-55967014 | Rare:88 | ||||
| chr12:56041533-56042020 | Common:4; Rare:103; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:56104397-56104824 | Common:5; Rare:150 | ||||
| chr12:56106691-56107229 | Common:1; Rare:89 | ||||
| chr12:56116511-56116748 | Common:2; Rare:95 | ||||
| chr12:56116760-56117268 | Common:5; Rare:141 | ||||
| chr12:56118002-56118295 | Rare:94 | ||||
| chr12:56127891-56128352 | Rare:102 |