| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123436579-123436769 | Common:2; Rare:64 | ||||
| chr12:123457870-123458244 | Common:3; Rare:156 | ||||
| chr12:123458202-123458700 | Common:8; Rare:181 | ||||
| chr12:123532890-123533410 | Common:6; Rare:206 | ||||
| chr12:123533594-123534358 | Common:13; Rare:445 | ||||
| chr12:123584235-123584822 | Common:24; Rare:485 | ||||
| chr12:123585049-123585723 | Common:8; Rare:250 | ||||
| chr12:123601911-123602354 | Common:11; Rare:270 | ||||
| chr12:123633549-123633917 | Common:5; Rare:447; Clinvar:24; Clinvar (benign):3 | ||||
| chr12:123670864-123671260 | Common:11; Rare:192; Clinvar:3; Clinvar (benign):3 | ||||
| chr12:123712102-123712492 | Common:20; Rare:351; Clinvar:7; Clinvar (benign):6 | ||||
| chr12:123972297-123973401 | Common:21; Rare:868 | ||||
| chr12:124388685-124389102 | Common:10; Rare:283 | ||||
| chr12:124389249-124389502 | Rare:145 | ||||
| chr12:124422225-124422365 | Common:2; Rare:27 |