| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:34238100-34238470 | Common:10; Rare:236 | ||||
| chr6:34248987-34249311 | Common:2; Rare:160 | ||||
| chr6:34392348-34392452 | Rare:48 | ||||
| chr6:34392485-34392903 | Common:2; Rare:200 | ||||
| chr6:34425991-34426201 | Common:9; Rare:161; Clinvar:2; Clinvar (benign):16 | ||||
| chr6:34696706-34696993 | Common:2; Rare:130 | ||||
| chr6:34757285-34757577 | Common:3; Rare:150 | ||||
| chr6:34791907-34792143 | Common:7; Rare:123 | ||||
| chr6:34887907-34888135 | Common:2; Rare:99 | ||||
| chr6:34889082-34889361 | Common:5; Rare:108 | ||||
| chr6:34889560-34889840 | Common:3; Rare:114 | ||||
| chr6:35258590-35258990 | Common:1; Rare:96 | ||||
| chr6:35259151-35259796 | Common:8; Rare:364 | ||||
| chr6:35452120-35452384 | Rare:72 | ||||
| chr6:35452570-35452703 | Rare:27; Clinvar:4 |