| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:137219284-137219511 | Common:4; Rare:79; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr6:137867026-137867382 | Rare:82 | ||||
| chr6:138773345-138773547 | Common:2; Rare:93 | ||||
| chr6:138773645-138773836 | Common:3; Rare:88 | ||||
| chr6:138988216-138988380 | Common:2; Rare:45 | ||||
| chr6:139028441-139028842 | Common:2; Rare:78 | ||||
| chr6:139374446-139374667 | Common:2; Rare:104 | ||||
| chr6:142147140-142147294 | Rare:58 | ||||
| chr6:142301847-142302157 | Common:6; Rare:90 | ||||
| chr6:142945032-142945234 | Common:1; Rare:60 | ||||
| chr6:143060308-143060488 | Common:1; Rare:46 | ||||
| chr6:143060697-143060935 | Common:7; Rare:82 | ||||
| chr6:143450651-143450970 | Common:1; Rare:115; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:143511621-143511779 | Common:4; Rare:36 | ||||
| chr6:143843179-143843402 | Common:2; Rare:72 |