| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41832876-41833235 | Common:3; Rare:121 | ||||
| chr22:42614866-42615244 | Common:3; Rare:152 | ||||
| chr22:42649333-42649482 | Common:1; Rare:58 | ||||
| chr22:45163804-45164008 | Common:2; Rare:73 | ||||
| chr22:46053794-46053901 | Rare:38 | ||||
| chr22:46267832-46268027 | Common:1; Rare:57 | ||||
| chr22:46335621-46335760 | Common:2; Rare:57; Clinvar:4; Clinvar (benign):6 | ||||
| chr22:46762517-46762660 | Common:3; Rare:47 | ||||
| chr22:50783665-50783830 | Common:1; Rare:46 | ||||
| chr3:3126773-3126984 | Common:4; Rare:91; Clinvar (benign):1 | ||||
| chr3:9363018-9363098 | Rare:29 | ||||
| chr3:9792740-9793108 | Common:3; Rare:126 | ||||
| chr3:10026360-10026459 | Rare:25 | ||||
| chr3:10141680-10141834 | Common:1; Rare:63; Clinvar:4; Clinvar (benign):14 | ||||
| chr3:12484389-12484511 | Common:1; Rare:37; Clinvar (benign):1 |