| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:3752095-3752212 | Common:1; Rare:35 | ||||
| chr6:4021124-4021446 | Common:1; Rare:123 | ||||
| chr6:4021636-4021939 | Common:2; Rare:84 | ||||
| chr6:4134039-4134507 | Common:2; Rare:142 | ||||
| chr6:4135521-4135813 | Common:8; Rare:70 | ||||
| chr6:4136084-4136317 | Common:1; Rare:69 | ||||
| chr6:4776045-4776438 | Common:5; Rare:99 | ||||
| chr6:4776703-4777088 | Common:5; Rare:108 | ||||
| chr6:5003589-5003850 | Common:6; Rare:85 | ||||
| chr6:5004008-5004205 | Common:2; Rare:86 | ||||
| chr6:5260686-5261069 | Common:6; Rare:134; Clinvar (benign):4 | ||||
| chr6:5261246-5261579 | Common:9; Rare:88 | ||||
| chr6:5261741-5262141 | Common:11; Rare:105 | ||||
| chr6:7107712-7107946 | Common:1; Rare:77 | ||||
| chr6:7107948-7108174 | Common:1; Rare:53 |