| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:189789446-189789762 | Common:5; Rare:47 | ||||
| chr3:190120371-190120730 | Common:1; Rare:162; Clinvar (pathogenic):1 | ||||
| chr3:190120889-190121004 | Rare:40 | ||||
| chr3:190321970-190322552 | Common:4; Rare:171; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr3:190513903-190514113 | Common:2; Rare:61 | ||||
| chr3:193554847-193555046 | Rare:40 | ||||
| chr3:194136253-194136654 | Common:2; Rare:127 | ||||
| chr3:196287563-196287771 | Rare:62 | ||||
| chr3:196318197-196318324 | Common:1; Rare:56 | ||||
| chr3:196567958-196568187 | Rare:36 | ||||
| chr3:196568518-196568756 | Common:5; Rare:74 | ||||
| chr3:196639496-196639794 | Common:2; Rare:70 | ||||
| chr3:196942333-196942654 | Common:1; Rare:138 | ||||
| chr3:197736840-197737140 | Common:3; Rare:95 | ||||
| chr3:197749821-197750036 | Rare:83 |