| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:167573474-167573808 | Common:4; Rare:61 | ||||
| chr5:167573894-167574016 | Common:1; Rare:29 | ||||
| chr5:168529111-168529305 | Common:3; Rare:40 | ||||
| chr5:168579617-168579942 | Common:2; Rare:80 | ||||
| chr5:169583592-169583901 | Common:7; Rare:89 | ||||
| chr5:171387498-171388006 | Common:1; Rare:239; Clinvar:1 | ||||
| chr5:172006503-172006960 | Common:2; Rare:126 | ||||
| chr5:172454324-172454675 | Common:12; Rare:99; Clinvar:1; Clinvar (benign):3 | ||||
| chr5:172771182-172771431 | Common:4; Rare:106 | ||||
| chr5:172958600-172958743 | Common:1; Rare:42 | ||||
| chr5:172959287-172959689 | Common:3; Rare:117 | ||||
| chr5:173056145-173056415 | Common:1; Rare:76 | ||||
| chr5:173057121-173057363 | Common:1; Rare:63 | ||||
| chr5:173328412-173328596 | Rare:34 | ||||
| chr5:173888105-173888438 | Common:2; Rare:102 |