| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:133080610-133081007 | Common:8; Rare:317 | ||||
| chr12:133130224-133130700 | Common:20; Rare:407 | ||||
| chr12:133181334-133181602 | Common:2; Rare:80 | ||||
| chr13:19633396-19633961 | Common:5; Rare:452 | ||||
| chr13:19782514-19783163 | Common:8; Rare:372 | ||||
| chr13:19863381-19864237 | Common:22; Rare:732 | ||||
| chr13:19958358-19959144 | Common:27; Rare:848 | ||||
| chr13:19959668-19960029 | Common:2; Rare:110 | ||||
| chr13:20160980-20161460 | Common:7; Rare:232; Clinvar (benign):1 | ||||
| chr13:20524794-20525688 | Common:15; Rare:309 | ||||
| chr13:20525735-20526011 | Common:4; Rare:228 | ||||
| chr13:20526150-20526488 | Common:8; Rare:96 | ||||
| chr13:20566862-20567336 | Common:4; Rare:308 | ||||
| chr13:20567352-20567601 | Common:3; Rare:104 | ||||
| chr13:20702900-20703320 | Common:3; Rare:118 |