| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:139028628-139028875 | Common:1; Rare:52 | ||||
| chr6:139029041-139029146 | Common:4; Rare:24 | ||||
| chr6:139374276-139374667 | Common:3; Rare:156 | ||||
| chr6:142147120-142147294 | Common:3; Rare:64 | ||||
| chr6:142945032-142945339 | Common:1; Rare:81 | ||||
| chr6:143060377-143060516 | Rare:32 | ||||
| chr6:143060683-143060983 | Common:9; Rare:110 | ||||
| chr6:143450642-143451033 | Common:1; Rare:139; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:143511245-143511313 | Rare:13 | ||||
| chr6:143511621-143511782 | Common:4; Rare:38 | ||||
| chr6:143677857-143678203 | Common:1; Rare:85 | ||||
| chr6:143843179-143843453 | Common:2; Rare:90 | ||||
| chr6:144150386-144150592 | Common:3; Rare:61 | ||||
| chr6:144284870-144285740 | Common:6; Rare:225 | ||||
| chr6:144330598-144330932 | Common:3; Rare:60 |