| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:52989157-52989419 | Common:4; Rare:70; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:53109714-53109890 | Common:1; Rare:90; Clinvar:4 | ||||
| chr5:54310517-54310711 | Rare:61 | ||||
| chr5:55307637-55308015 | Common:4; Rare:126 | ||||
| chr5:55994784-55995134 | Common:1; Rare:113 | ||||
| chr5:56909466-56909627 | Common:2; Rare:45 | ||||
| chr5:56952100-56952304 | Rare:74 | ||||
| chr5:57173569-57173888 | Common:2; Rare:115 | ||||
| chr5:58459742-58460246 | Common:7; Rare:193 | ||||
| chr5:59768493-59768587 | Rare:23 | ||||
| chr5:59768628-59768742 | Rare:32 | ||||
| chr5:60700123-60700237 | Common:1; Rare:38 | ||||
| chr5:60945026-60945249 | Common:5; Rare:84; Clinvar:3; Clinvar (benign):5 | ||||
| chr5:61162271-61162497 | Common:1; Rare:46 | ||||
| chr5:62403462-62403544 | Rare:20 |