| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:12556966-12557180 | Common:4; Rare:78 | ||||
| chr3:12664065-12664499 | Common:3; Rare:110; Clinvar:1; Clinvar (benign):4 | ||||
| chr3:12967659-12968040 | Common:5; Rare:135 | ||||
| chr3:12994807-12995401 | Common:3; Rare:259 | ||||
| chr3:13420060-13420530 | Common:1; Rare:143 | ||||
| chr3:13479422-13479822 | Common:4; Rare:126 | ||||
| chr3:13479920-13480360 | Common:3; Rare:114 | ||||
| chr3:13880058-13880297 | Common:4; Rare:55 | ||||
| chr3:14124329-14124434 | Common:1; Rare:32 | ||||
| chr3:14124868-14125145 | Common:3; Rare:87; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178546-14178895 | Common:2; Rare:186; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14402395-14402625 | Common:1; Rare:63 | ||||
| chr3:14403025-14403249 | Common:3; Rare:45 | ||||
| chr3:14651385-14651841 | Common:1; Rare:145 | ||||
| chr3:14947334-14947587 | Common:3; Rare:118 |