| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:179819390-179819820 | Common:3; Rare:153 | ||||
| chr5:179820746-179820922 | Common:6; Rare:130; Clinvar:1; Clinvar (benign):4 | ||||
| chr5:179821580-179822070 | Common:6; Rare:139 | ||||
| chr5:179858789-179859033 | Rare:223 | ||||
| chr5:179907809-179908053 | Common:5; Rare:211 | ||||
| chr5:180071698-180071818 | Rare:50 | ||||
| chr5:180291973-180292251 | Common:2; Rare:220 | ||||
| chr5:180494163-180494558 | Common:8; Rare:263 | ||||
| chr5:180494860-180495110 | Common:4; Rare:140 | ||||
| chr5:180810068-180810276 | Common:8; Rare:117 | ||||
| chr5:180810445-180810610 | Common:4; Rare:111 | ||||
| chr5:181223118-181223333 | Rare:141 | ||||
| chr5:181223370-181223960 | Common:9; Rare:194 | ||||
| chr5:181243705-181243982 | Common:8; Rare:188 | ||||
| chr5:181244145-181244556 | Common:6; Rare:157 |