| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:43602852-43602953 | Rare:21 | ||||
| chr5:43603045-43603283 | Rare:58 | ||||
| chr5:44388891-44389173 | Common:1; Rare:58 | ||||
| chr5:44389366-44389648 | Rare:38 | ||||
| chr5:44389689-44389945 | Common:1; Rare:53 | ||||
| chr5:44808659-44809032 | Common:2; Rare:133 | ||||
| chr5:44809398-44809502 | Rare:50 | ||||
| chr5:50667344-50667442 | Common:1; Rare:31 | ||||
| chr5:50667767-50667983 | Common:1; Rare:66 | ||||
| chr5:51383242-51383465 | Common:2; Rare:93 | ||||
| chr5:52787820-52787974 | Common:1; Rare:30 | ||||
| chr5:52989216-52989358 | Common:4; Rare:40; Clinvar (benign):1 | ||||
| chr5:53109716-53109926 | Common:1; Rare:105; Clinvar:3 | ||||
| chr5:54310507-54310717 | Common:1; Rare:68 | ||||
| chr5:55160048-55160208 | Rare:41 |