| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9749789-9750057 | Common:2; Rare:157 | ||||
| chr3:9750100-9750380 | Common:2; Rare:171 | ||||
| chr3:9792376-9792645 | Rare:136 | ||||
| chr3:9792650-9793127 | Common:7; Rare:320 | ||||
| chr3:9809450-9809770 | Common:2; Rare:137 | ||||
| chr3:9810070-9810350 | Common:1; Rare:148 | ||||
| chr3:9843868-9844173 | Common:6; Rare:215 | ||||
| chr3:9890442-9890898 | Common:6; Rare:277; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr3:9916896-9917158 | Common:4; Rare:78 | ||||
| chr3:9933511-9933912 | Common:4; Rare:233; Clinvar:3 | ||||
| chr3:9986478-9987223 | Common:15; Rare:431 | ||||
| chr3:10026295-10026496 | Rare:109 | ||||
| chr3:10115491-10115753 | Common:8; Rare:177 | ||||
| chr3:10141651-10142009 | Common:4; Rare:323; Clinvar:77; Clinvar (benign):67 | ||||
| chr3:10164852-10165013 | Rare:70 |