| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:7389740-7389888 | Common:1; Rare:44 | ||||
| chr6:7541171-7541337 | Common:1; Rare:43 | ||||
| chr6:7541396-7541910 | Common:1; Rare:154; Clinvar:3; Clinvar (benign):2 | ||||
| chr6:7590077-7590300 | Common:5; Rare:84 | ||||
| chr6:7910734-7910850 | Common:1; Rare:47 | ||||
| chr6:8064295-8064555 | Common:4; Rare:92 | ||||
| chr6:8102437-8102778 | Common:2; Rare:116 | ||||
| chr6:8435379-8435673 | Common:5; Rare:106 | ||||
| chr6:10521208-10521257 | Rare:16 | ||||
| chr6:10556039-10556267 | Common:1; Rare:49; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:10585547-10585811 | Common:3; Rare:61 | ||||
| chr6:10694567-10695125 | Common:7; Rare:179 | ||||
| chr6:10722857-10723224 | Common:6; Rare:124 | ||||
| chr6:10747493-10747860 | Common:4; Rare:130 | ||||
| chr6:10838487-10838709 | Common:4; Rare:58; Clinvar:4 |