| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:135497594-135497934 | Common:4; Rare:124; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:136250230-136250568 | Common:2; Rare:103 | ||||
| chr6:136289733-136290061 | Common:2; Rare:143 | ||||
| chr6:136550331-136550709 | Common:2; Rare:114 | ||||
| chr6:137866931-137867214 | Rare:60 | ||||
| chr6:138107410-138107616 | Common:5; Rare:54 | ||||
| chr6:138161835-138161998 | Common:4; Rare:56 | ||||
| chr6:138404122-138404538 | Common:6; Rare:119 | ||||
| chr6:138692386-138692513 | Common:1; Rare:31 | ||||
| chr6:138773701-138773836 | Common:3; Rare:68 | ||||
| chr6:138915272-138915445 | Common:1; Rare:25 | ||||
| chr6:138987312-138987359 | Common:1; Rare:10 | ||||
| chr6:138987913-138988076 | Common:3; Rare:39 | ||||
| chr6:139028322-139028530 | Common:1; Rare:36 | ||||
| chr6:139028626-139028849 | Common:1; Rare:47 |