| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:163459763-163460165 | Common:2; Rare:154 | ||||
| chr5:163460360-163460660 | Common:5; Rare:66 | ||||
| chr5:163505444-163505674 | Common:1; Rare:75 | ||||
| chr5:167573502-167574022 | Common:6; Rare:98 | ||||
| chr5:168486382-168486497 | Common:1; Rare:39; Clinvar (benign):1 | ||||
| chr5:168578967-168579163 | Common:1; Rare:50 | ||||
| chr5:169583609-169583889 | Common:7; Rare:83 | ||||
| chr5:171387560-171388006 | Rare:214; Clinvar:1 | ||||
| chr5:172454318-172454661 | Common:10; Rare:96; Clinvar:1; Clinvar (benign):3 | ||||
| chr5:172834163-172834433 | Common:1; Rare:65 | ||||
| chr5:172958534-172958750 | Common:3; Rare:69 | ||||
| chr5:172958801-172958938 | Common:3; Rare:39 | ||||
| chr5:172959311-172959687 | Common:3; Rare:113 | ||||
| chr5:173056126-173056407 | Common:1; Rare:76 | ||||
| chr5:173888157-173888404 | Rare:75 |