| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:144286175-144286358 | Common:1; Rare:39 | ||||
| chr6:145814700-145814921 | Common:1; Rare:104 | ||||
| chr6:149546003-149546159 | Rare:66 | ||||
| chr6:149749617-149749796 | Rare:98 | ||||
| chr6:151452070-151452548 | Common:3; Rare:171 | ||||
| chr6:152302080-152302237 | Rare:50 | ||||
| chr6:152983022-152983327 | Common:2; Rare:96 | ||||
| chr6:152983516-152983743 | Common:3; Rare:87 | ||||
| chr6:153002687-153002838 | Common:2; Rare:47 | ||||
| chr6:158168210-158168382 | Common:2; Rare:59 | ||||
| chr6:158644700-158644943 | Common:2; Rare:94 | ||||
| chr6:158818209-158818351 | Common:3; Rare:54 | ||||
| chr6:158999761-158999886 | Common:1; Rare:47; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:159693235-159693467 | Common:4; Rare:74 | ||||
| chr6:159726918-159727164 | Common:1; Rare:94 |