| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:37257603-37257827 | Rare:59 | ||||
| chr6:37258111-37258334 | Common:3; Rare:35 | ||||
| chr6:37433184-37433300 | Common:1; Rare:27 | ||||
| chr6:41072443-41072737 | Rare:81 | ||||
| chr6:41921083-41921515 | Common:3; Rare:107 | ||||
| chr6:42050354-42050567 | Common:1; Rare:71 | ||||
| chr6:42746071-42746348 | Rare:77 | ||||
| chr6:42879585-42879940 | Rare:101 | ||||
| chr6:42929209-42929582 | Common:4; Rare:112 | ||||
| chr6:43013878-43014280 | Common:2; Rare:88 | ||||
| chr6:43427809-43427925 | Rare:34 | ||||
| chr6:43516778-43517112 | Common:6; Rare:117; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575952-43576190 | Rare:95; Clinvar:4 | ||||
| chr6:43629143-43629451 | Common:2; Rare:89 | ||||
| chr6:44126799-44126933 | Rare:40 |