| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:21588840-21589086 | Common:2; Rare:47 | ||||
| chr6:21589284-21589297 | Rare:4 | ||||
| chr6:21593503-21593909 | Common:1; Rare:101 | ||||
| chr6:21594547-21594942 | Common:1; Rare:103; Clinvar (pathogenic):1 | ||||
| chr6:21595075-21595202 | Rare:38 | ||||
| chr6:21595246-21595361 | Rare:44 | ||||
| chr6:21666333-21666444 | Rare:28 | ||||
| chr6:21771628-21771812 | Common:4; Rare:34 | ||||
| chr6:21823385-21823460 | Rare:14 | ||||
| chr6:21948038-21948059 | Rare:2 | ||||
| chr6:21984257-21984271 | Rare:1 | ||||
| chr6:21987577-21987713 | Common:1; Rare:30 | ||||
| chr6:22025163-22025455 | Common:3; Rare:47 | ||||
| chr6:22025707-22025927 | Rare:45 | ||||
| chr6:22078931-22079074 | Common:1; Rare:23 |