| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:40798123-40798407 | Common:2; Rare:192 | ||||
| chr5:40835144-40835473 | Common:7; Rare:255 | ||||
| chr5:40835617-40835787 | Common:2; Rare:41 | ||||
| chr5:40841086-40841382 | Rare:61 | ||||
| chr5:41869450-41870090 | Common:1; Rare:149 | ||||
| chr5:41870364-41870606 | Common:2; Rare:81; Clinvar:2; Clinvar (benign):2 | ||||
| chr5:41904000-41904394 | Common:4; Rare:198 | ||||
| chr5:41925163-41925351 | Common:3; Rare:123 | ||||
| chr5:43064934-43065175 | Common:2; Rare:114 | ||||
| chr5:43066819-43067093 | Common:1; Rare:97 | ||||
| chr5:43067130-43067890 | Rare:211 | ||||
| chr5:43120828-43121125 | Common:9; Rare:210 | ||||
| chr5:43121330-43121677 | Common:2; Rare:226 | ||||
| chr5:43313298-43313681 | Common:6; Rare:164 | ||||
| chr5:43483110-43483610 | Common:4; Rare:184 |