| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:156327067-156327222 | Common:1; Rare:33; Clinvar:3; Clinvar (benign):2 | ||||
| chr5:157731359-157731486 | Common:4; Rare:53 | ||||
| chr5:157858929-157859233 | Common:2; Rare:95 | ||||
| chr5:159207585-159208038 | Common:1; Rare:130 | ||||
| chr5:159208107-159208255 | Common:1; Rare:30 | ||||
| chr5:159263184-159263349 | Common:1; Rare:51 | ||||
| chr5:160400026-160400221 | Common:4; Rare:59 | ||||
| chr5:160419022-160419275 | Common:4; Rare:94 | ||||
| chr5:160421682-160422063 | Common:4; Rare:105 | ||||
| chr5:163437287-163437784 | Common:1; Rare:138 | ||||
| chr5:163460053-163460165 | Common:2; Rare:47 | ||||
| chr5:163460372-163460698 | Common:6; Rare:76 | ||||
| chr5:163503133-163503378 | Common:1; Rare:61 | ||||
| chr5:163505426-163505661 | Common:1; Rare:76 | ||||
| chr5:168486324-168486519 | Common:3; Rare:68; Clinvar (benign):3; Clinvar (pathogenic):3 |