| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:6632946-6633499 | Common:10; Rare:171; Clinvar:10; Clinvar (benign):6 | ||||
| chr5:6712726-6713037 | Common:7; Rare:106 | ||||
| chr5:6713135-6713534 | Common:3; Rare:128 | ||||
| chr5:7868929-7869236 | Common:2; Rare:162; Clinvar:2; Clinvar (benign):3 | ||||
| chr5:10249404-10249503 | Common:2; Rare:17 | ||||
| chr5:10249592-10249704 | Common:1; Rare:19 | ||||
| chr5:10249736-10249897 | Rare:74 | ||||
| chr5:10250202-10250584 | Common:3; Rare:173; Clinvar:5; Clinvar (benign):2 | ||||
| chr5:10250755-10250805 | Rare:11 | ||||
| chr5:10307515-10307643 | Common:1; Rare:28 | ||||
| chr5:10353235-10353360 | Rare:24 | ||||
| chr5:10353366-10353975 | Common:5; Rare:206 | ||||
| chr5:10441763-10441862 | Rare:19 | ||||
| chr5:10564055-10564107 | Rare:8 | ||||
| chr5:10564110-10564397 | Common:2; Rare:88 |