| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:44809190-44810081 | Common:10; Rare:776 | ||||
| chr5:44810248-44810654 | Common:4; Rare:173 | ||||
| chr5:51383230-51383500 | Common:4; Rare:195 | ||||
| chr5:53109619-53110019 | Common:8; Rare:750; Clinvar:21; Clinvar (pathogenic):2 | ||||
| chr5:53110204-53110604 | Common:3; Rare:78 | ||||
| chr5:53560587-53561195 | Common:12; Rare:439; Clinvar:6; Clinvar (benign):9; Clinvar (pathogenic):3 | ||||
| chr5:54309459-54310171 | Rare:246 | ||||
| chr5:54310388-54310841 | Common:12; Rare:680 | ||||
| chr5:54310776-54311179 | Common:8; Rare:226 | ||||
| chr5:54517490-54517785 | Common:6; Rare:164 | ||||
| chr5:54517726-54517852 | Common:1; Rare:59 | ||||
| chr5:54518220-54518590 | Common:4; Rare:153 | ||||
| chr5:55159970-55161045 | Common:3; Rare:292 | ||||
| chr5:55173090-55173803 | Common:13; Rare:276 | ||||
| chr5:55226340-55226770 | Rare:109; Clinvar:1; Clinvar (benign):3 |