| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:134175709-134175747 | Rare:9 | ||||
| chr6:135497592-135497882 | Common:4; Rare:105; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:136038261-136038451 | Common:1; Rare:49 | ||||
| chr6:136289755-136290014 | Common:1; Rare:111 | ||||
| chr6:137866941-137867259 | Rare:75 | ||||
| chr6:138773657-138773825 | Common:3; Rare:82 | ||||
| chr6:142147140-142147290 | Rare:56 | ||||
| chr6:142945161-142945350 | Common:1; Rare:46 | ||||
| chr6:143060738-143061061 | Common:8; Rare:113 | ||||
| chr6:143450573-143450936 | Common:1; Rare:133; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:144285145-144285626 | Common:3; Rare:129 | ||||
| chr6:145814662-145814927 | Common:1; Rare:118 | ||||
| chr6:149749695-149749851 | Rare:78 | ||||
| chr6:149863997-149864126 | Common:2; Rare:32 | ||||
| chr6:151452035-151452552 | Common:4; Rare:183 |