| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:144285249-144285665 | Common:2; Rare:99 | ||||
| chr6:145814649-145814927 | Common:1; Rare:120 | ||||
| chr6:145815143-145815366 | Common:1; Rare:41 | ||||
| chr6:148342936-148343214 | Common:1; Rare:103 | ||||
| chr6:149545989-149546123 | Rare:58 | ||||
| chr6:149718016-149718122 | Common:1; Rare:41 | ||||
| chr6:149749658-149749811 | Rare:83 | ||||
| chr6:150599821-150599931 | Rare:47 | ||||
| chr6:151240240-151240434 | Common:1; Rare:53 | ||||
| chr6:151390943-151391078 | Common:1; Rare:43 | ||||
| chr6:151391500-151391849 | Common:3; Rare:102 | ||||
| chr6:151452026-151452552 | Common:5; Rare:185; Clinvar (benign):2 | ||||
| chr6:152983487-152983750 | Common:4; Rare:97 | ||||
| chr6:153002513-153002838 | Common:5; Rare:126 | ||||
| chr6:154510233-154510596 | Common:4; Rare:78 |