| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:134174840-134175032 | Common:1; Rare:94 | ||||
| chr6:135054784-135054980 | Common:6; Rare:57 | ||||
| chr6:135497600-135497936 | Common:4; Rare:127; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:136289766-136290040 | Common:1; Rare:119 | ||||
| chr6:136526053-136526295 | Common:3; Rare:47 | ||||
| chr6:136526570-136526660 | Common:1; Rare:19 | ||||
| chr6:136550395-136550687 | Common:2; Rare:83 | ||||
| chr6:137219310-137219515 | Common:4; Rare:71; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr6:138773689-138773836 | Common:3; Rare:72 | ||||
| chr6:139028416-139028850 | Common:2; Rare:83 | ||||
| chr6:142147113-142147300 | Common:3; Rare:70 | ||||
| chr6:143060374-143060500 | Rare:28 | ||||
| chr6:143060724-143060927 | Common:7; Rare:71 | ||||
| chr6:143450660-143450929 | Common:1; Rare:101; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:143511632-143511855 | Common:4; Rare:53 |