| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:15601502-15601764 | Common:4; Rare:105; Clinvar:1 | ||||
| chr3:15859732-15860115 | Common:4; Rare:125 | ||||
| chr3:16264842-16265243 | Common:2; Rare:138 | ||||
| chr3:19946980-19947183 | Common:4; Rare:75 | ||||
| chr3:23916919-23917230 | Rare:115 | ||||
| chr3:25783390-25783622 | Common:2; Rare:77; Clinvar (benign):3 | ||||
| chr3:29280831-29281076 | Common:3; Rare:48 | ||||
| chr3:33096755-33097053 | Common:2; Rare:91; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):4 | ||||
| chr3:33798509-33798705 | Common:2; Rare:71 | ||||
| chr3:36993078-36993557 | Common:2; Rare:164; Clinvar:26; Clinvar (benign):12; Clinvar (pathogenic):3 | ||||
| chr3:37176116-37176381 | Common:1; Rare:70 | ||||
| chr3:37861711-37861873 | Rare:37 | ||||
| chr3:39107562-39107708 | Common:3; Rare:46 | ||||
| chr3:39383289-39383437 | Common:2; Rare:24; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:39383538-39383660 | Rare:26; Clinvar:2 |