| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:89117944-89118097 | Common:1; Rare:62 | ||||
| chr6:89145973-89146090 | Rare:34 | ||||
| chr6:89352614-89353008 | Common:2; Rare:92 | ||||
| chr6:89638443-89638544 | Common:1; Rare:22 | ||||
| chr6:89638701-89638813 | Common:4; Rare:42 | ||||
| chr6:89819688-89819863 | Rare:59 | ||||
| chr6:89829595-89829973 | Common:1; Rare:99 | ||||
| chr6:90587018-90587349 | Common:2; Rare:88 | ||||
| chr6:93419552-93419890 | Common:1; Rare:90 | ||||
| chr6:95577356-95577602 | Common:6; Rare:71 | ||||
| chr6:96521674-96521871 | Common:8; Rare:95 | ||||
| chr6:96897803-96898089 | Common:4; Rare:106; Clinvar:3; Clinvar (benign):1 | ||||
| chr6:97283135-97283302 | Common:1; Rare:54 | ||||
| chr6:99424874-99424933 | Rare:22 | ||||
| chr6:99425234-99425452 | Common:2; Rare:64 |