| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:130366188-130366421 | Common:3; Rare:49 | ||||
| chr6:131628105-131628422 | Common:3; Rare:87 | ||||
| chr6:132814274-132814597 | Common:3; Rare:111 | ||||
| chr6:134052633-134052797 | Common:1; Rare:25 | ||||
| chr6:134174843-134174968 | Rare:54 | ||||
| chr6:135497693-135497860 | Common:3; Rare:69; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:136289767-136290041 | Common:2; Rare:119 | ||||
| chr6:136550361-136550695 | Common:2; Rare:101 | ||||
| chr6:137219334-137219493 | Common:2; Rare:55; Clinvar (benign):2 | ||||
| chr6:138404147-138404564 | Common:7; Rare:113 | ||||
| chr6:138773583-138773827 | Common:3; Rare:102 | ||||
| chr6:139028333-139028530 | Common:1; Rare:35 | ||||
| chr6:139028632-139028850 | Common:1; Rare:46 | ||||
| chr6:142147061-142147290 | Common:3; Rare:82 | ||||
| chr6:143060603-143060935 | Common:10; Rare:118 |