| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:50628069-50628295 | Common:9; Rare:105; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50783592-50783862 | Common:2; Rare:87 | ||||
| chr3:3126808-3126990 | Common:4; Rare:79; Clinvar (benign):2 | ||||
| chr3:4303277-4303412 | Common:1; Rare:60 | ||||
| chr3:4467231-4467325 | Rare:39; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:4493169-4493520 | Rare:122; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:4980284-4980538 | Rare:57 | ||||
| chr3:5187283-5187735 | Common:5; Rare:174 | ||||
| chr3:8501620-8501935 | Common:2; Rare:119 | ||||
| chr3:9249633-9249816 | Common:2; Rare:45 | ||||
| chr3:9362936-9363160 | Common:2; Rare:73 | ||||
| chr3:9397422-9397912 | Common:1; Rare:155 | ||||
| chr3:9749839-9750073 | Common:1; Rare:76 | ||||
| chr3:9769871-9770018 | Common:1; Rare:42 | ||||
| chr3:9792382-9792570 | Rare:52 |