| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:10307190-10308301 | Common:20; Rare:988 | ||||
| chr5:10353114-10353430 | Common:2; Rare:121 | ||||
| chr5:10353362-10354017 | Common:26; Rare:1041 | ||||
| chr5:10353980-10354672 | Common:11; Rare:356 | ||||
| chr5:10441642-10442042 | Common:2; Rare:295 | ||||
| chr5:10564060-10564460 | Common:6; Rare:337 | ||||
| chr5:10760751-10761151 | Common:6; Rare:156 | ||||
| chr5:10761082-10761823 | Common:79; Rare:791 | ||||
| chr5:14142989-14143999 | Common:2; Rare:578; Clinvar:2 | ||||
| chr5:14664320-14665094 | Common:29; Rare:988 | ||||
| chr5:14871501-14872105 | Common:12; Rare:342; Clinvar (benign):2 | ||||
| chr5:16465559-16466051 | Common:5; Rare:492 | ||||
| chr5:16466131-16466531 | Common:1; Rare:72 | ||||
| chr5:27120412-27121408 | Common:16; Rare:423 | ||||
| chr5:31531438-31532015 | Common:3; Rare:144 |