| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:196941992-196942156 | Common:3; Rare:42 | ||||
| chr3:196942355-196942686 | Common:1; Rare:141 | ||||
| chr3:197003944-197004225 | Common:1; Rare:79 | ||||
| chr3:197260683-197260744 | Rare:8 | ||||
| chr3:197736829-197737232 | Common:3; Rare:132 | ||||
| chr3:197749329-197749432 | Common:1; Rare:22 | ||||
| chr3:197749763-197750061 | Common:1; Rare:102 | ||||
| chr3:197750706-197750766 | Rare:15 | ||||
| chr3:197949840-197950291 | Common:4; Rare:131; Clinvar (benign):2 | ||||
| chr3:197950854-197950975 | Rare:32; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:197959967-197960251 | Common:1; Rare:101 | ||||
| chr4:337462-337837 | Common:1; Rare:98 | ||||
| chr4:499059-499333 | Common:3; Rare:110 | ||||
| chr4:527448-527759 | Common:4; Rare:66 | ||||
| chr4:673832-673990 | Rare:66 |