| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:73520890-73521148 | Rare:39 | ||||
| chr3:73521156-73521547 | Rare:67 | ||||
| chr3:73625456-73625466 | Rare:2 | ||||
| chr3:75435013-75435378 | Common:4; Rare:126 | ||||
| chr3:75641095-75641402 | Common:1; Rare:47 | ||||
| chr3:81761498-81761605 | Common:5; Rare:35; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:101576733-101576939 | Common:2; Rare:40 | ||||
| chr3:101576980-101577022 | Rare:8 | ||||
| chr3:101676282-101676517 | Common:1; Rare:80 | ||||
| chr3:107240577-107240765 | Rare:80 | ||||
| chr3:112639947-112639953 | Rare:5 | ||||
| chr3:112640326-112640429 | Common:1; Rare:15 | ||||
| chr3:123413183-123413415 | Common:1; Rare:52 | ||||
| chr3:123447442-123447571 | Common:1; Rare:44 | ||||
| chr3:123447998-123448240 | Common:1; Rare:74; Clinvar (pathogenic):1 |