| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:131063155-131063467 | Rare:93 | ||||
| chr6:131628146-131628302 | Common:1; Rare:49 | ||||
| chr6:133241162-133241438 | Common:4; Rare:84 | ||||
| chr6:133953047-133953255 | Common:2; Rare:67 | ||||
| chr6:134174857-134175059 | Common:1; Rare:95 | ||||
| chr6:135054784-135054990 | Common:6; Rare:62 | ||||
| chr6:135497604-135497897 | Common:4; Rare:107; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:136289767-136290032 | Common:1; Rare:115 | ||||
| chr6:137219334-137219516 | Common:4; Rare:63; Clinvar (benign):2 | ||||
| chr6:138773646-138773831 | Common:3; Rare:86 | ||||
| chr6:139291938-139292051 | Rare:13 | ||||
| chr6:142147140-142147285 | Rare:52 | ||||
| chr6:143060700-143060935 | Common:7; Rare:82 | ||||
| chr6:143450654-143450929 | Common:1; Rare:103; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:143677732-143678062 | Common:2; Rare:77 |