| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:41870481-41870669 | Common:2; Rare:45; Clinvar:2; Clinvar (benign):2 | ||||
| chr5:41903961-41904381 | Common:2; Rare:128 | ||||
| chr5:42811853-42812190 | Common:1; Rare:65 | ||||
| chr5:43064833-43065143 | Common:1; Rare:73 | ||||
| chr5:43067438-43067499 | Rare:10 | ||||
| chr5:43121416-43121697 | Common:1; Rare:101 | ||||
| chr5:43313110-43313242 | Rare:25 | ||||
| chr5:43313364-43313509 | Common:3; Rare:44 | ||||
| chr5:43483831-43483996 | Common:1; Rare:55 | ||||
| chr5:43484328-43484360 | Rare:7 | ||||
| chr5:43484367-43484670 | Rare:72 | ||||
| chr5:43515035-43515302 | Common:4; Rare:96 | ||||
| chr5:43556348-43556426 | Common:1; Rare:27 | ||||
| chr5:43556842-43556912 | Common:2; Rare:35 | ||||
| chr5:43602542-43602753 | Common:2; Rare:40 |