| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:37861703-37861975 | Common:1; Rare:57 | ||||
| chr3:38024506-38024718 | Common:1; Rare:78 | ||||
| chr3:38165015-38165262 | Common:1; Rare:51 | ||||
| chr3:38165437-38165666 | Common:1; Rare:79 | ||||
| chr3:38165787-38165895 | Rare:42 | ||||
| chr3:39107537-39107732 | Common:4; Rare:61 | ||||
| chr3:39383283-39383427 | Common:1; Rare:26; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:39383582-39383660 | Rare:17; Clinvar:1 | ||||
| chr3:40309491-40309824 | Common:9; Rare:117 | ||||
| chr3:40457212-40457388 | Common:3; Rare:88 | ||||
| chr3:42581874-42582113 | Common:2; Rare:78 | ||||
| chr3:42600522-42600751 | Common:1; Rare:90 | ||||
| chr3:43690823-43691032 | Common:5; Rare:116; Clinvar:9; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:44477622-44477733 | Common:1; Rare:27 | ||||
| chr3:44624836-44625101 | Common:2; Rare:73 |