| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:138773316-138773540 | Common:3; Rare:93 | ||||
| chr6:138773677-138773819 | Common:3; Rare:73 | ||||
| chr6:138988263-138988432 | Common:1; Rare:38 | ||||
| chr6:139028334-139028538 | Common:1; Rare:35 | ||||
| chr6:139028606-139028832 | Common:1; Rare:48 | ||||
| chr6:139374536-139374779 | Common:1; Rare:104 | ||||
| chr6:142147140-142147302 | Rare:65 | ||||
| chr6:142301842-142302205 | Common:6; Rare:102 | ||||
| chr6:142302407-142302690 | Common:1; Rare:56 | ||||
| chr6:143060731-143060935 | Common:7; Rare:74 | ||||
| chr6:143450597-143450971 | Common:1; Rare:134; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:143511647-143511806 | Common:4; Rare:38 | ||||
| chr6:143843196-143843480 | Common:2; Rare:96 | ||||
| chr6:144095501-144095840 | Common:6; Rare:101 | ||||
| chr6:144150285-144150529 | Common:5; Rare:70 |