| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:163505447-163505766 | Common:1; Rare:109 | ||||
| chr5:163505828-163505888 | Common:2; Rare:10 | ||||
| chr5:167573540-167573708 | Rare:23 | ||||
| chr5:168486391-168486530 | Common:3; Rare:57; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
| chr5:168579276-168579659 | Common:3; Rare:119 | ||||
| chr5:168579745-168579811 | Rare:14 | ||||
| chr5:169583569-169583907 | Common:7; Rare:109 | ||||
| chr5:169583964-169584113 | Common:3; Rare:35 | ||||
| chr5:170297681-170297767 | Common:1; Rare:17 | ||||
| chr5:170389289-170389533 | Common:3; Rare:41 | ||||
| chr5:170861836-170862032 | Common:1; Rare:70 | ||||
| chr5:171143138-171143328 | Common:1; Rare:28 | ||||
| chr5:171387498-171388033 | Common:1; Rare:252; Clinvar:1 | ||||
| chr5:172006498-172007049 | Common:2; Rare:164 | ||||
| chr5:172115088-172115278 | Rare:53 |