| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:197750033-197750191 | Rare:41 | ||||
| chr3:197791074-197791381 | Common:3; Rare:119 | ||||
| chr3:197791458-197791499 | Rare:10 | ||||
| chr3:197912826-197913403 | Common:17; Rare:151 | ||||
| chr3:197916363-197916542 | Rare:29 | ||||
| chr3:197949870-197950260 | Common:4; Rare:115; Clinvar (benign):2 | ||||
| chr3:197950654-197950978 | Common:1; Rare:74; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:197959979-197960287 | Common:1; Rare:117 | ||||
| chr4:53093-53424 | Rare:5 | ||||
| chr4:124440-124554 | Common:3; Rare:38 | ||||
| chr4:124673-124798 | Common:2; Rare:35 | ||||
| chr4:305410-305620 | Common:2; Rare:75 | ||||
| chr4:337415-337914 | Common:6; Rare:142 | ||||
| chr4:474040-474330 | Common:3; Rare:97 | ||||
| chr4:499100-499351 | Common:3; Rare:108 |