| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:124422655-124422816 | Common:2; Rare:40 | ||||
| chr12:124914820-124915066 | Common:3; Rare:103 | ||||
| chr12:130871771-130872122 | Common:4; Rare:140 | ||||
| chr12:131710795-131711119 | Rare:87 | ||||
| chr12:131929021-131929277 | Common:10; Rare:78; Clinvar:1 | ||||
| chr12:132687311-132687707 | Common:4; Rare:148; Clinvar:5; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr12:132887558-132887810 | Rare:76 | ||||
| chr13:19782927-19783088 | Common:2; Rare:57 | ||||
| chr13:19863448-19863649 | Common:3; Rare:66 | ||||
| chr13:20525796-20525977 | Common:1; Rare:66 | ||||
| chr13:20773932-20774034 | Rare:34 | ||||
| chr13:21140418-21140614 | Rare:98 | ||||
| chr13:21176478-21176708 | Common:2; Rare:100 | ||||
| chr13:24160509-24160764 | Rare:71 | ||||
| chr13:24512728-24512862 | Common:3; Rare:39 |