| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:130002213-130002366 | Rare:66 | ||||
| chr11:130002742-130003360 | Common:7; Rare:316 | ||||
| chr11:130069558-130070074 | Common:4; Rare:346 | ||||
| chr11:130314320-130314800 | Common:2; Rare:180 | ||||
| chr11:130314878-130315030 | Common:4; Rare:103 | ||||
| chr11:134223906-134224166 | Common:4; Rare:156 | ||||
| chr11:134224515-134224761 | Rare:197 | ||||
| chr11:134253292-134253594 | Common:4; Rare:198; Clinvar (benign):2 | ||||
| chr12:389224-389391 | Common:1; Rare:106 | ||||
| chr12:389437-389720 | Common:12; Rare:202 | ||||
| chr12:401436-401677 | Rare:128 | ||||
| chr12:752305-752636 | Common:2; Rare:188 | ||||
| chr12:949440-950111 | Common:16; Rare:300 | ||||
| chr12:990250-990560 | Common:5; Rare:134 | ||||
| chr12:990660-991010 | Common:3; Rare:152 |