| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:74684935-74685361 | Common:17; Rare:482; Clinvar:14; Clinvar (benign):12 | ||||
| chr5:74766215-74766615 | Common:6; Rare:144 | ||||
| chr5:74766689-74767478 | Common:20; Rare:712; Clinvar (benign):1 | ||||
| chr5:74767530-74767930 | Common:2; Rare:107 | ||||
| chr5:75236239-75236690 | Common:1; Rare:130 | ||||
| chr5:75236710-75237302 | Common:31; Rare:554 | ||||
| chr5:75336162-75336562 | Common:4; Rare:131 | ||||
| chr5:75336779-75337324 | Common:20; Rare:805 | ||||
| chr5:75338021-75338390 | Rare:67 | ||||
| chr5:75338587-75338824 | Common:1; Rare:29 | ||||
| chr5:75510718-75511290 | Common:2; Rare:269; Clinvar:1 | ||||
| chr5:75511535-75512111 | Common:15; Rare:898 | ||||
| chr5:75716713-75717228 | Common:3; Rare:186 | ||||
| chr5:75717270-75717778 | Common:40; Rare:713 | ||||
| chr5:76402470-76402963 | Common:20; Rare:263 |