| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:65602730-65602887 | Common:1; Rare:22 | ||||
| chr12:84911161-84911463 | Common:2; Rare:56 | ||||
| chr12:110698695-110698850 | Rare:29 | ||||
| chr12:116495392-116495659 | Common:2; Rare:47 | ||||
| chr12:120291900-120292191 | Common:8; Rare:115 | ||||
| chr12:124390810-124390938 | Rare:36 | ||||
| chr12:124423100-124423340 | Common:2; Rare:67 | ||||
| chr12:127060366-127060627 | Common:4; Rare:84 | ||||
| chr12:127230915-127231147 | Common:2; Rare:37 | ||||
| chr13:23888726-23888872 | Common:1; Rare:39 | ||||
| chr13:44309742-44309993 | Common:2; Rare:47 | ||||
| chr13:90839622-90839936 | Common:5; Rare:86 | ||||
| chr14:49633949-49634098 | Common:1; Rare:70; Clinvar:9; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr14:49862713-49863048 | Rare:152 | ||||
| chr14:51534553-51534863 | Rare:46 |