| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:46267835-46268032 | Common:1; Rare:58 | ||||
| chr22:49918284-49918736 | Common:5; Rare:160; Clinvar (benign):3 | ||||
| chr22:50525532-50525758 | Common:5; Rare:121; Clinvar:4; Clinvar (benign):2 | ||||
| chr22:50582412-50582455 | Rare:20 | ||||
| chr22:50582777-50583176 | Common:9; Rare:143; Clinvar:2; Clinvar (benign):3 | ||||
| chr22:50783598-50783822 | Common:2; Rare:73 | ||||
| chr3:8501644-8501932 | Common:2; Rare:106 | ||||
| chr3:9362935-9363098 | Common:2; Rare:57 | ||||
| chr3:9792388-9792583 | Rare:53 | ||||
| chr3:9792719-9793121 | Common:3; Rare:142 | ||||
| chr3:9933507-9933893 | Common:3; Rare:154; Clinvar:3 | ||||
| chr3:10026295-10026414 | Rare:43 | ||||
| chr3:13568422-13568781 | Common:6; Rare:75 | ||||
| chr3:14124689-14125145 | Common:4; Rare:132; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178530-14178861 | Common:2; Rare:171; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):1 |