| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:44127276-44127721 | Common:8; Rare:227 | ||||
| chr6:44219355-44219647 | Rare:65 | ||||
| chr6:44229420-44229730 | Rare:142 | ||||
| chr6:44246875-44247193 | Common:7; Rare:223 | ||||
| chr6:44256834-44257234 | Common:5; Rare:166 | ||||
| chr6:44257480-44257636 | Rare:42 | ||||
| chr6:44387407-44387753 | Common:8; Rare:162 | ||||
| chr6:44387890-44388390 | Common:15; Rare:207 | ||||
| chr6:45377170-45377674 | Common:5; Rare:184 | ||||
| chr6:45377715-45378220 | Common:5; Rare:280 | ||||
| chr6:46652685-46653031 | Rare:160 | ||||
| chr6:47309030-47309780 | Common:6; Rare:221 | ||||
| chr6:47477589-47477860 | Common:2; Rare:147; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:47478067-47478264 | Common:4; Rare:138; Clinvar:4; Clinvar (benign):6 | ||||
| chr6:49463122-49463440 | Common:2; Rare:171; Clinvar:3; Clinvar (benign):2 |