| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:171387512-171388006 | Rare:234; Clinvar:1 | ||||
| chr5:172006555-172006950 | Common:2; Rare:100 | ||||
| chr5:172188186-172188459 | Rare:74 | ||||
| chr5:172454362-172454655 | Common:10; Rare:76; Clinvar:1; Clinvar (benign):3 | ||||
| chr5:172770579-172770931 | Common:3; Rare:94 | ||||
| chr5:172770969-172771014 | Rare:15 | ||||
| chr5:172771044-172771074 | Rare:3 | ||||
| chr5:172771079-172771512 | Common:6; Rare:162 | ||||
| chr5:172834163-172834422 | Common:1; Rare:63 | ||||
| chr5:172959362-172959475 | Common:2; Rare:40 | ||||
| chr5:173057119-173057363 | Common:1; Rare:63 | ||||
| chr5:173328342-173328605 | Rare:54 | ||||
| chr5:173888115-173888384 | Rare:80 | ||||
| chr5:173890432-173890576 | Rare:32 | ||||
| chr5:173890577-173890636 | Rare:22 |