| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:1799769-1799977 | Common:8; Rare:101 | ||||
| chr5:1801281-1801545 | Common:4; Rare:136; Clinvar:3; Clinvar (benign):3 | ||||
| chr5:5422364-5422722 | Common:2; Rare:120 | ||||
| chr5:6378362-6378678 | Rare:112 | ||||
| chr5:6632661-6632843 | Common:3; Rare:82; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr5:6632887-6633530 | Common:11; Rare:197; Clinvar:10; Clinvar (benign):7 | ||||
| chr5:7868991-7869229 | Common:2; Rare:125; Clinvar:1; Clinvar (benign):3 | ||||
| chr5:10249863-10250442 | Common:19; Rare:270; Clinvar:5; Clinvar (benign):2 | ||||
| chr5:10307581-10307721 | Common:1; Rare:33 | ||||
| chr5:10307743-10307927 | Rare:39 | ||||
| chr5:10353564-10353920 | Common:4; Rare:138 | ||||
| chr5:10354036-10354156 | Rare:40 | ||||
| chr5:10354266-10354480 | Common:3; Rare:52 | ||||
| chr5:10441803-10441946 | Rare:42 | ||||
| chr5:10564157-10564381 | Common:1; Rare:70 |