| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:134374383-134374681 | Common:2; Rare:150 | ||||
| chr3:134485915-134486286 | Common:7; Rare:226 | ||||
| chr3:136195510-136196020 | Common:5; Rare:301 | ||||
| chr3:136196231-136196780 | Common:2; Rare:374 | ||||
| chr3:136196814-136196971 | Rare:86 | ||||
| chr3:136250226-136250372 | Common:5; Rare:103; Clinvar:4; Clinvar (benign):4 | ||||
| chr3:136250430-136250790 | Common:6; Rare:204; Clinvar:7; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr3:136751579-136751932 | Common:8; Rare:256 | ||||
| chr3:136752203-136752753 | Common:3; Rare:284 | ||||
| chr3:136818937-136819228 | Common:8; Rare:243 | ||||
| chr3:136861989-136862322 | Common:2; Rare:202 | ||||
| chr3:136862639-136862900 | Common:4; Rare:75 | ||||
| chr3:136957711-136958045 | Common:2; Rare:122 | ||||
| chr3:138114940-138115370 | Common:2; Rare:161 | ||||
| chr3:138115564-138115730 | Common:8; Rare:70 |