| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:69369163-69369896 | Common:5; Rare:274 | ||||
| chr5:69369933-69370067 | Common:1; Rare:29 | ||||
| chr5:69492659-69492797 | Rare:48; Clinvar (benign):1 | ||||
| chr5:69560097-69560290 | Common:3; Rare:49 | ||||
| chr5:70049560-70049677 | Rare:13 | ||||
| chr5:71455536-71456007 | Common:1; Rare:159; Clinvar (benign):1 | ||||
| chr5:71587137-71587440 | Common:1; Rare:105; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:72107144-72107715 | Common:2; Rare:198 | ||||
| chr5:72308329-72308615 | Common:3; Rare:81 | ||||
| chr5:72816492-72816740 | Common:4; Rare:94 | ||||
| chr5:72847998-72848265 | Common:3; Rare:83 | ||||
| chr5:72955854-72956091 | Common:1; Rare:107 | ||||
| chr5:73498278-73498745 | Common:3; Rare:153 | ||||
| chr5:73498750-73498790 | Rare:13 | ||||
| chr5:73565352-73565899 | Common:7; Rare:164 |