| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:82278256-82278754 | Common:25; Rare:843 | ||||
| chr5:82278933-82279333 | Common:3; Rare:82 | ||||
| chr5:82279433-82280046 | Common:8; Rare:145 | ||||
| chr5:83077250-83077681 | Common:7; Rare:744 | ||||
| chr5:83077765-83077866 | Common:2; Rare:26 | ||||
| chr5:83077867-83078320 | Common:6; Rare:199 | ||||
| chr5:86617710-86618071 | Common:10; Rare:474 | ||||
| chr5:86618260-86618520 | Common:3; Rare:101 | ||||
| chr5:87267520-87268410 | Common:31; Rare:1294; Clinvar:4; Clinvar (benign):6 | ||||
| chr5:87268390-87269092 | Common:4; Rare:695; Clinvar:26; Clinvar (benign):23; Clinvar (pathogenic):5 | ||||
| chr5:87412083-87412554 | Rare:227 | ||||
| chr5:87412638-87413247 | Common:28; Rare:801 | ||||
| chr5:88251192-88251451 | Common:1; Rare:41 | ||||
| chr5:88268550-88269507 | Common:1; Rare:1233 | ||||
| chr5:88784950-88785350 | Common:5; Rare:79 |