| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:72848043-72848248 | Common:3; Rare:67 | ||||
| chr5:72955854-72956091 | Common:1; Rare:107 | ||||
| chr5:73498298-73498688 | Common:3; Rare:130 | ||||
| chr5:73498780-73498947 | Common:1; Rare:50 | ||||
| chr5:73565306-73565899 | Common:8; Rare:173 | ||||
| chr5:74640723-74640916 | Common:1; Rare:60 | ||||
| chr5:74685108-74685422 | Common:2; Rare:119; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr5:74685432-74685549 | Common:2; Rare:42; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:74713237-74713635 | Common:3; Rare:102; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):4 | ||||
| chr5:74720590-74720675 | Common:1; Rare:33; Clinvar:1; Clinvar (pathogenic):3 | ||||
| chr5:74766847-74767363 | Common:3; Rare:141; Clinvar (benign):1 | ||||
| chr5:75236848-75237110 | Common:6; Rare:92 | ||||
| chr5:75336349-75336570 | Common:2; Rare:41 | ||||
| chr5:75336840-75337297 | Common:4; Rare:151 | ||||
| chr5:75511591-75512086 | Common:3; Rare:151 |