| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:173047245-173047463 | Common:1; Rare:39 | ||||
| chr5:176392817-176393226 | Common:3; Rare:70 | ||||
| chr5:176591680-176591839 | Common:6; Rare:21 | ||||
| chr5:176592514-176592760 | Common:1; Rare:76 | ||||
| chr5:177503243-177503502 | Common:1; Rare:75 | ||||
| chr5:177546405-177546656 | Common:1; Rare:43 | ||||
| chr5:177618156-177618341 | Common:7; Rare:31 | ||||
| chr5:177672172-177672326 | Common:5; Rare:26 | ||||
| chr5:177939465-177939642 | Common:1; Rare:33 | ||||
| chr5:178206439-178206876 | Common:2; Rare:128 | ||||
| chr5:178209851-178210178 | Common:1; Rare:103 | ||||
| chr5:178211955-178212024 | Rare:28; Clinvar (pathogenic):1 | ||||
| chr5:178213886-178213918 | Rare:6 | ||||
| chr5:178213993-178214142 | Rare:29 | ||||
| chr5:178228898-178229027 | Common:1; Rare:27 |