| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:159765672-159765988 | Rare:62 | ||||
| chr3:160515198-160515489 | Common:1; Rare:61 | ||||
| chr3:169765015-169765195 | Rare:87; Clinvar:6; Clinvar (pathogenic):3 | ||||
| chr3:177756423-177756487 | Rare:7 | ||||
| chr3:184322700-184322954 | Rare:64 | ||||
| chr3:188217174-188217366 | Common:2; Rare:31 | ||||
| chr3:188220565-188220603 | Rare:5 | ||||
| chr3:188231088-188231266 | Common:2; Rare:28 | ||||
| chr3:188266031-188266334 | Rare:59 | ||||
| chr3:188636689-188636818 | Common:2; Rare:53 | ||||
| chr3:194583904-194584020 | Common:4; Rare:40 | ||||
| chr3:195657857-195658144 | Common:13; Rare:47 | ||||
| chr3:196431255-196431387 | Common:2; Rare:15 | ||||
| chr3:196632616-196632844 | Common:2; Rare:62 | ||||
| chr3:197627833-197628017 | Common:6; Rare:69 |