| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:145735254-145735546 | Common:7; Rare:85; Clinvar:16; Clinvar (benign):12 | ||||
| chr6:145814647-145814927 | Common:1; Rare:121 | ||||
| chr6:145814976-145815352 | Common:2; Rare:82 | ||||
| chr6:145964217-145964445 | Common:1; Rare:66 | ||||
| chr6:148342924-148343178 | Common:1; Rare:92 | ||||
| chr6:149546010-149546126 | Rare:50 | ||||
| chr6:149749555-149749796 | Rare:113 | ||||
| chr6:151239691-151239991 | Rare:60 | ||||
| chr6:151240234-151240252 | Rare:3 | ||||
| chr6:151240277-151240416 | Common:1; Rare:39 | ||||
| chr6:151325409-151325780 | Common:2; Rare:83 | ||||
| chr6:151390954-151391163 | Common:2; Rare:62 | ||||
| chr6:151391511-151391864 | Common:3; Rare:98 | ||||
| chr6:151452035-151452538 | Common:4; Rare:176 | ||||
| chr6:152983516-152983756 | Common:4; Rare:91 |