| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:156826122-156826374 | Common:3; Rare:79 | ||||
| chr3:157159825-157159897 | Rare:18 | ||||
| chr3:157159985-157160343 | Rare:151 | ||||
| chr3:157543226-157543400 | Rare:41 | ||||
| chr3:158109836-158110149 | Rare:68 | ||||
| chr3:158644505-158644653 | Common:5; Rare:57; Clinvar (benign):6 | ||||
| chr3:158672545-158672740 | Common:2; Rare:58 | ||||
| chr3:158732151-158732319 | Common:6; Rare:51 | ||||
| chr3:158801991-158802224 | Common:3; Rare:104 | ||||
| chr3:158804134-158804370 | Rare:51 | ||||
| chr3:160399175-160399307 | Rare:35; Clinvar:2 | ||||
| chr3:160399512-160399669 | Rare:34 | ||||
| chr3:160400400-160400576 | Common:2; Rare:42 | ||||
| chr3:160565260-160565842 | Common:3; Rare:193 | ||||
| chr3:160755448-160755683 | Common:1; Rare:87 |