| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:124746755-124746972 | Common:5; Rare:39 | ||||
| chr5:124748753-124749051 | Common:3; Rare:65 | ||||
| chr5:126595160-126595372 | Common:4; Rare:98; Clinvar:5; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr5:126600849-126600994 | Common:1; Rare:69 | ||||
| chr5:126776915-126777184 | Common:1; Rare:105; Clinvar:4; Clinvar (benign):2 | ||||
| chr5:127030509-127030736 | Common:2; Rare:54 | ||||
| chr5:127290677-127290860 | Rare:39 | ||||
| chr5:127517490-127517736 | Common:7; Rare:106 | ||||
| chr5:127517772-127517946 | Common:2; Rare:40 | ||||
| chr5:128083583-128083766 | Common:2; Rare:75 | ||||
| chr5:128538021-128538074 | Common:1; Rare:13; Clinvar (benign):2 | ||||
| chr5:128538076-128538372 | Common:6; Rare:90 | ||||
| chr5:128965398-128965590 | Common:2; Rare:53 | ||||
| chr5:129094498-129094892 | Common:3; Rare:176 | ||||
| chr5:129459995-129460373 | Common:4; Rare:78 |