| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:50400754-50401041 | Common:1; Rare:94 | ||||
| chr12:50401296-50401436 | Common:1; Rare:33 | ||||
| chr12:50763913-50764345 | Common:1; Rare:119 | ||||
| chr12:50764356-50764501 | Common:2; Rare:47 | ||||
| chr12:50842964-50843047 | Common:1; Rare:29 | ||||
| chr12:50843094-50843128 | Rare:20 | ||||
| chr12:50923857-50924080 | Common:2; Rare:43 | ||||
| chr12:50924322-50924783 | Common:3; Rare:106 | ||||
| chr12:51009148-51009356 | Common:1; Rare:38 | ||||
| chr12:51026297-51026488 | Common:2; Rare:88; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:51048059-51048398 | Common:2; Rare:116 | ||||
| chr12:51172780-51172949 | Common:2; Rare:39 | ||||
| chr12:51173074-51173243 | Rare:30 | ||||
| chr12:51238609-51238915 | Common:8; Rare:123 | ||||
| chr12:51239152-51239306 | Common:2; Rare:43 |