| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:39073887-39074114 | Common:5; Rare:62 | ||||
| chr5:39074336-39074501 | Common:1; Rare:77 | ||||
| chr5:39425126-39425308 | Common:2; Rare:47 | ||||
| chr5:40679714-40679938 | Common:1; Rare:49 | ||||
| chr5:40798094-40798281 | Rare:76 | ||||
| chr5:40835184-40835325 | Common:2; Rare:61 | ||||
| chr5:41870360-41870591 | Common:2; Rare:77; Clinvar:3; Clinvar (benign):2 | ||||
| chr5:41904003-41904379 | Common:2; Rare:116 | ||||
| chr5:42424889-42424992 | Rare:22 | ||||
| chr5:43064855-43065141 | Common:1; Rare:68 | ||||
| chr5:43067357-43067517 | Rare:22 | ||||
| chr5:43120817-43120967 | Common:3; Rare:71 | ||||
| chr5:43121404-43121660 | Common:1; Rare:98 | ||||
| chr5:43313364-43313503 | Common:3; Rare:42 | ||||
| chr5:43483831-43483980 | Common:1; Rare:50 |