| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:186930172-186930571 | Common:3; Rare:97 | ||||
| chr3:186930679-186930727 | Rare:12 | ||||
| chr3:186930735-186930760 | Rare:6 | ||||
| chr3:186931273-186931354 | Common:1; Rare:21 | ||||
| chr3:187139355-187139564 | Common:2; Rare:71 | ||||
| chr3:188153575-188153992 | Common:1; Rare:79 | ||||
| chr3:188154060-188154227 | Rare:53 | ||||
| chr3:191329218-191329605 | Common:3; Rare:112 | ||||
| chr3:192917840-192918033 | Common:2; Rare:84 | ||||
| chr3:193593086-193593382 | Rare:97; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:194486970-194487146 | Common:4; Rare:88 | ||||
| chr3:194632803-194633102 | Common:1; Rare:74 | ||||
| chr3:194672125-194672622 | Common:4; Rare:151 | ||||
| chr3:195543209-195543485 | Common:3; Rare:105 | ||||
| chr3:196082060-196082259 | Common:2; Rare:76 |