| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:137219113-137219226 | Common:1; Rare:38; Clinvar:1 | ||||
| chr6:137219319-137219496 | Common:2; Rare:60; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr6:138404147-138404589 | Common:7; Rare:124 | ||||
| chr6:138545652-138545871 | Common:1; Rare:40 | ||||
| chr6:138773385-138773586 | Common:2; Rare:104 | ||||
| chr6:138773646-138773836 | Common:3; Rare:88 | ||||
| chr6:139028638-139028870 | Common:1; Rare:50 | ||||
| chr6:139374536-139374782 | Common:1; Rare:105 | ||||
| chr6:142147129-142147284 | Common:1; Rare:53 | ||||
| chr6:142301832-142302330 | Common:6; Rare:136 | ||||
| chr6:143060700-143060927 | Common:7; Rare:77 | ||||
| chr6:143450651-143450929 | Common:1; Rare:105; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:143843220-143843427 | Common:2; Rare:62 | ||||
| chr6:144150324-144150529 | Common:5; Rare:58 | ||||
| chr6:144285249-144285378 | Common:2; Rare:31 |