| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:44223441-44223615 | Common:1; Rare:51 | ||||
| chr6:44246890-44247193 | Common:4; Rare:129 | ||||
| chr6:44387449-44387575 | Common:2; Rare:28 | ||||
| chr6:44387675-44387778 | Common:1; Rare:37 | ||||
| chr6:45377649-45377698 | Common:1; Rare:17 | ||||
| chr6:45421905-45422116 | Common:2; Rare:58 | ||||
| chr6:46015481-46015686 | Rare:53 | ||||
| chr6:46015698-46015927 | Common:2; Rare:49 | ||||
| chr6:46129777-46130182 | Common:5; Rare:127 | ||||
| chr6:46652748-46653022 | Rare:70 | ||||
| chr6:46735336-46735502 | Common:1; Rare:47 | ||||
| chr6:47309585-47309705 | Common:1; Rare:16 | ||||
| chr6:47309862-47310091 | Common:1; Rare:52 | ||||
| chr6:47477664-47478278 | Common:5; Rare:183; Clinvar:7; Clinvar (benign):8 | ||||
| chr6:49463141-49463393 | Common:1; Rare:70; Clinvar:1; Clinvar (benign):1 |