| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:5261238-5261633 | Common:10; Rare:107 | ||||
| chr6:6320592-6320769 | Rare:57; Clinvar:1 | ||||
| chr6:6588595-6588801 | Common:1; Rare:67 | ||||
| chr6:7107527-7107916 | Common:1; Rare:130 | ||||
| chr6:7108573-7108684 | Rare:38 | ||||
| chr6:7313049-7313380 | Common:5; Rare:125 | ||||
| chr6:7389740-7389976 | Common:1; Rare:61 | ||||
| chr6:7541368-7541710 | Common:1; Rare:103; Clinvar (benign):1 | ||||
| chr6:8102511-8102706 | Common:1; Rare:66 | ||||
| chr6:8435342-8435701 | Common:6; Rare:124 | ||||
| chr6:8435854-8435908 | Common:1; Rare:9 | ||||
| chr6:10412151-10412317 | Rare:57 | ||||
| chr6:10694586-10694988 | Common:5; Rare:113 | ||||
| chr6:10722836-10723241 | Common:6; Rare:138 | ||||
| chr6:10747608-10747865 | Common:3; Rare:102 |