| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:134846650-134846970 | Common:1; Rare:75 | ||||
| chr5:134874196-134874598 | Common:1; Rare:169 | ||||
| chr5:134874778-134875112 | Common:2; Rare:55 | ||||
| chr5:134904643-134904924 | Rare:74 | ||||
| chr5:134905045-134905210 | Common:1; Rare:45 | ||||
| chr5:134905390-134905740 | Common:1; Rare:91 | ||||
| chr5:135399222-135399329 | Rare:29 | ||||
| chr5:135535957-135536247 | Common:3; Rare:49 | ||||
| chr5:136132668-136132961 | Common:1; Rare:94 | ||||
| chr5:136133256-136133656 | Common:3; Rare:129 | ||||
| chr5:137735640-137736330 | Common:2; Rare:134; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:137754314-137754520 | Rare:70 | ||||
| chr5:137754671-137754980 | Common:1; Rare:115 | ||||
| chr5:137888258-137888658 | Common:2; Rare:73 | ||||
| chr5:138032580-138032830 | Common:2; Rare:56 |