| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:128520569-128520798 | Common:1; Rare:86 | ||||
| chr6:131063148-131063482 | Rare:98 | ||||
| chr6:131628166-131628428 | Common:2; Rare:72 | ||||
| chr6:132401452-132401570 | Common:1; Rare:35 | ||||
| chr6:132513057-132513246 | Rare:46 | ||||
| chr6:135054774-135054990 | Common:6; Rare:66 | ||||
| chr6:135497649-135497873 | Common:4; Rare:88; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:136289747-136290063 | Common:2; Rare:141 | ||||
| chr6:137219350-137219502 | Common:3; Rare:49; Clinvar (benign):2 | ||||
| chr6:138404181-138404512 | Common:4; Rare:97 | ||||
| chr6:138773689-138773813 | Common:3; Rare:61 | ||||
| chr6:139028648-139028853 | Common:1; Rare:44 | ||||
| chr6:142147140-142147284 | Rare:51 | ||||
| chr6:143060569-143060686 | Common:4; Rare:32 | ||||
| chr6:143060731-143060920 | Common:7; Rare:65 |