| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:189940613-189941011 | Common:14; Rare:144 | ||||
| chr5:218112-218415 | Common:3; Rare:121; Clinvar:11; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
| chr5:443095-443263 | Common:8; Rare:75 | ||||
| chr5:892623-892923 | Common:5; Rare:101 | ||||
| chr5:1799791-1799988 | Common:4; Rare:92 | ||||
| chr5:1801286-1801460 | Common:4; Rare:87; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:6378492-6378669 | Rare:76 | ||||
| chr5:6633295-6633724 | Common:3; Rare:130; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:7868993-7869212 | Common:2; Rare:112; Clinvar (benign):1 | ||||
| chr5:10249859-10250436 | Common:19; Rare:270; Clinvar:5; Clinvar (benign):2 | ||||
| chr5:10307586-10307686 | Rare:23 | ||||
| chr5:10307743-10308049 | Common:1; Rare:60 | ||||
| chr5:10353564-10353905 | Common:4; Rare:133 | ||||
| chr5:14664602-14664914 | Common:2; Rare:126 | ||||
| chr5:16465644-16465895 | Rare:60 |