| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9397376-9397953 | Common:3; Rare:186 | ||||
| chr3:9397990-9398126 | Common:1; Rare:34 | ||||
| chr3:9649200-9649586 | Common:1; Rare:129 | ||||
| chr3:9731710-9731825 | Common:1; Rare:54 | ||||
| chr3:9732258-9732459 | Rare:59 | ||||
| chr3:9749676-9750111 | Common:1; Rare:128 | ||||
| chr3:9750187-9750362 | Common:1; Rare:70 | ||||
| chr3:9792322-9793159 | Common:4; Rare:277 | ||||
| chr3:9793531-9793662 | Rare:29 | ||||
| chr3:9809249-9809298 | Rare:14 | ||||
| chr3:9809675-9809795 | Common:1; Rare:31 | ||||
| chr3:9810019-9810323 | Common:1; Rare:109 | ||||
| chr3:9843898-9844307 | Common:4; Rare:152 | ||||
| chr3:9890402-9890710 | Common:4; Rare:123 | ||||
| chr3:9890778-9890816 | Rare:12; Clinvar:1; Clinvar (pathogenic):1 |