| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:146447005-146447374 | Common:2; Rare:92 | ||||
| chr5:146878274-146878462 | Rare:43 | ||||
| chr5:146878687-146879139 | Common:5; Rare:100; Clinvar (benign):1 | ||||
| chr5:147234872-147235095 | Common:2; Rare:61 | ||||
| chr5:147453920-147454074 | Common:1; Rare:39 | ||||
| chr5:147454114-147454207 | Common:1; Rare:31 | ||||
| chr5:148383771-148384029 | Rare:76 | ||||
| chr5:149345332-149345595 | Common:1; Rare:101 | ||||
| chr5:149550283-149550339 | Rare:6 | ||||
| chr5:149551356-149551646 | Rare:70 | ||||
| chr5:149960627-149960934 | Rare:100; Clinvar:7 | ||||
| chr5:150289728-150289961 | Common:2; Rare:51 | ||||
| chr5:150357448-150357749 | Rare:103; Clinvar:2; Clinvar (benign):4 | ||||
| chr5:150449634-150449803 | Common:4; Rare:54 | ||||
| chr5:150671782-150672085 | Common:1; Rare:86 |