| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:39424847-39425308 | Common:3; Rare:113 | ||||
| chr5:40679298-40679409 | Common:1; Rare:24 | ||||
| chr5:40755810-40756044 | Rare:56 | ||||
| chr5:40798082-40798401 | Common:1; Rare:116 | ||||
| chr5:40835151-40835389 | Common:2; Rare:101 | ||||
| chr5:40841541-40841658 | Common:1; Rare:36 | ||||
| chr5:41869766-41870073 | Rare:53 | ||||
| chr5:41870360-41870570 | Common:1; Rare:71; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:41903979-41904399 | Common:2; Rare:136 | ||||
| chr5:42423362-42423518 | Common:1; Rare:36 | ||||
| chr5:43043170-43043315 | Common:1; Rare:28 | ||||
| chr5:43064833-43065149 | Common:1; Rare:75 | ||||
| chr5:43066950-43067120 | Rare:41 | ||||
| chr5:43067160-43067525 | Rare:63 | ||||
| chr5:43121396-43121667 | Common:1; Rare:104 |