| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:163437292-163437607 | Rare:88 | ||||
| chr5:163460049-163460159 | Common:2; Rare:45 | ||||
| chr5:163460372-163460671 | Common:5; Rare:65 | ||||
| chr5:163503242-163503366 | Common:1; Rare:37 | ||||
| chr5:163505413-163505648 | Common:1; Rare:71 | ||||
| chr5:168486350-168486510 | Common:3; Rare:58; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
| chr5:169583592-169583837 | Common:6; Rare:80 | ||||
| chr5:171387512-171387910 | Rare:187 | ||||
| chr5:172771191-172771489 | Common:5; Rare:114 | ||||
| chr5:172834163-172834433 | Common:1; Rare:65 | ||||
| chr5:172958801-172958945 | Common:4; Rare:41 | ||||
| chr5:172983704-172983863 | Common:1; Rare:60 | ||||
| chr5:173328412-173328605 | Rare:36 | ||||
| chr5:176361762-176361886 | Rare:32 | ||||
| chr5:176388556-176388811 | Common:4; Rare:99 |