| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:100401378-100401586 | Common:1; Rare:46 | ||||
| chr3:100492305-100492658 | Common:2; Rare:112 | ||||
| chr3:100709216-100709721 | Common:8; Rare:154; Clinvar (benign):1 | ||||
| chr3:101513093-101513356 | Common:8; Rare:67 | ||||
| chr3:101561743-101561989 | Common:2; Rare:88 | ||||
| chr3:101573958-101574267 | Common:2; Rare:114 | ||||
| chr3:101574618-101574850 | Common:2; Rare:64 | ||||
| chr3:101677039-101677404 | Rare:120 | ||||
| chr3:101686473-101686911 | Common:2; Rare:172 | ||||
| chr3:101724363-101724682 | Common:1; Rare:77 | ||||
| chr3:101779092-101779310 | Common:4; Rare:69 | ||||
| chr3:101779422-101779487 | Rare:17 | ||||
| chr3:105366562-105366941 | Common:3; Rare:109 | ||||
| chr3:105367193-105367420 | Common:2; Rare:62 | ||||
| chr3:105868754-105869202 | Common:7; Rare:145 |