| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:168288452-168288634 | Rare:40 | ||||
| chr5:168389366-168389576 | Common:5; Rare:37 | ||||
| chr5:168501783-168502104 | Common:1; Rare:76; Clinvar (benign):1 | ||||
| chr5:168505740-168506212 | Common:8; Rare:102; Clinvar (benign):5 | ||||
| chr5:169035337-169035640 | Common:2; Rare:56 | ||||
| chr5:171003576-171003853 | Common:3; Rare:53 | ||||
| chr5:172303691-172303979 | Common:3; Rare:57 | ||||
| chr5:172767372-172767425 | Rare:11 | ||||
| chr5:172770328-172770625 | Common:2; Rare:85 | ||||
| chr5:172908994-172909158 | Common:4; Rare:33 | ||||
| chr5:172953830-172954060 | Rare:37 | ||||
| chr5:173766425-173766728 | Common:2; Rare:49 | ||||
| chr5:175114805-175115051 | Common:3; Rare:47 | ||||
| chr5:175115072-175115102 | Rare:3 | ||||
| chr5:176355262-176355467 | Common:2; Rare:40 |