| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:13073411-13073582 | Common:5; Rare:56 | ||||
| chr3:13420222-13420470 | Common:1; Rare:73 | ||||
| chr3:14124729-14125061 | Common:4; Rare:92; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:14178573-14178863 | Common:2; Rare:150; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:14402335-14402622 | Common:1; Rare:80 | ||||
| chr3:14651468-14651813 | Rare:101 | ||||
| chr3:14947402-14947551 | Common:2; Rare:73 | ||||
| chr3:14948022-14948140 | Rare:63 | ||||
| chr3:15065233-15065349 | Common:2; Rare:45 | ||||
| chr3:15099128-15099299 | Rare:43 | ||||
| chr3:15427491-15427623 | Common:1; Rare:48 | ||||
| chr3:15601512-15601798 | Common:4; Rare:119; Clinvar:1 | ||||
| chr3:15601816-15602058 | Common:1; Rare:122; Clinvar:5; Clinvar (pathogenic):1 | ||||
| chr3:15859787-15860099 | Common:4; Rare:95 | ||||
| chr3:16264944-16265233 | Common:2; Rare:72 |