| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43575962-43576228 | Common:1; Rare:110; Clinvar:8 | ||||
| chr6:43770026-43770213 | Common:6; Rare:58 | ||||
| chr6:44127272-44127665 | Common:4; Rare:109 | ||||
| chr6:44246230-44246323 | Rare:26 | ||||
| chr6:49463167-49463401 | Common:1; Rare:69; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:52670979-52671236 | Rare:71 | ||||
| chr6:52995273-52995794 | Common:4; Rare:217 | ||||
| chr6:53348900-53349115 | Common:2; Rare:83 | ||||
| chr6:56542911-56543065 | Common:1; Rare:26 | ||||
| chr6:70566852-70566958 | Common:1; Rare:37 | ||||
| chr6:73520973-73521349 | Common:3; Rare:105 | ||||
| chr6:73523803-73523857 | Rare:18 | ||||
| chr6:73653956-73654162 | Common:3; Rare:57; Clinvar:2 | ||||
| chr6:73696016-73696213 | Common:1; Rare:40 | ||||
| chr6:75284711-75285022 | Common:1; Rare:91 |