| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:186806396-186806567 | Rare:55 | ||||
| chr3:187139387-187139587 | Common:2; Rare:73 | ||||
| chr3:188153771-188154224 | Common:1; Rare:108 | ||||
| chr3:188584304-188584409 | Common:2; Rare:19 | ||||
| chr3:188947637-188947751 | Rare:42 | ||||
| chr3:190116636-190116815 | Rare:34 | ||||
| chr3:190120250-190120688 | Common:1; Rare:190; Clinvar (pathogenic):1 | ||||
| chr3:190120853-190121050 | Rare:62 | ||||
| chr3:190121901-190122112 | Common:7; Rare:35 | ||||
| chr3:190122220-190122511 | Common:3; Rare:51 | ||||
| chr3:190122521-190122598 | Common:1; Rare:16 | ||||
| chr3:190322352-190322538 | Common:2; Rare:49 | ||||
| chr3:190513903-190514158 | Common:2; Rare:66 | ||||
| chr3:192917820-192918023 | Common:2; Rare:88 | ||||
| chr3:193593090-193593402 | Rare:97; Clinvar:2; Clinvar (benign):2 |