| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:43066900-43067089 | Rare:70 | ||||
| chr5:43120830-43120962 | Common:5; Rare:120 | ||||
| chr5:43120962-43121362 | Common:7; Rare:218 | ||||
| chr5:43121365-43121667 | Common:2; Rare:225 | ||||
| chr5:43313033-43313158 | Common:1; Rare:21 | ||||
| chr5:43313315-43313670 | Common:6; Rare:166 | ||||
| chr5:43483813-43483985 | Common:6; Rare:102 | ||||
| chr5:43515039-43515247 | Common:5; Rare:118 | ||||
| chr5:43556754-43556948 | Common:8; Rare:150 | ||||
| chr5:43556997-43557185 | Common:1; Rare:51 | ||||
| chr5:43602320-43602760 | Common:4; Rare:93 | ||||
| chr5:43603054-43603288 | Rare:114 | ||||
| chr5:44808715-44809026 | Common:4; Rare:225 | ||||
| chr5:52787863-52788292 | Common:2; Rare:167 | ||||
| chr5:52989170-52989484 | Common:8; Rare:185; Clinvar:2; Clinvar (benign):5 |