| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:127245147-127245411 | Common:4; Rare:66 | ||||
| chr9:127388271-127389158 | Common:5; Rare:303 | ||||
| chr9:127396551-127397400 | Common:11; Rare:335 | ||||
| chr9:127397575-127397975 | Common:3; Rare:125 | ||||
| chr9:127423989-127424143 | Rare:51 | ||||
| chr9:127424251-127424451 | Common:1; Rare:65 | ||||
| chr9:127449525-127449925 | Rare:118 | ||||
| chr9:127450887-127451287 | Common:5; Rare:174 | ||||
| chr9:127451382-127451609 | Common:2; Rare:60; Clinvar (benign):1 | ||||
| chr9:127569022-127569394 | Common:5; Rare:89 | ||||
| chr9:127611991-127612416 | Common:2; Rare:154; Clinvar:4; Clinvar (benign):4 | ||||
| chr9:127661380-127661700 | Common:1; Rare:64 | ||||
| chr9:127715605-127715850 | Common:2; Rare:102; Clinvar:1 | ||||
| chr9:127715920-127716190 | Rare:87 | ||||
| chr9:127734658-127734873 | Rare:36 |