| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:139029041-139029153 | Common:4; Rare:26 | ||||
| chr6:139134930-139135107 | Rare:42 | ||||
| chr6:142147120-142147321 | Common:3; Rare:88 | ||||
| chr6:143060581-143060736 | Common:4; Rare:50 | ||||
| chr6:143060752-143061057 | Common:7; Rare:109 | ||||
| chr6:143450561-143450944 | Common:1; Rare:141; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:143511252-143511304 | Rare:9 | ||||
| chr6:143511409-143511575 | Rare:57; Clinvar:1 | ||||
| chr6:143511611-143511843 | Common:4; Rare:54 | ||||
| chr6:143843136-143843478 | Common:2; Rare:117 | ||||
| chr6:144094903-144095074 | Common:1; Rare:34 | ||||
| chr6:144095081-144095131 | Rare:10 | ||||
| chr6:144095477-144095840 | Common:6; Rare:105 | ||||
| chr6:144285122-144285612 | Common:3; Rare:133 | ||||
| chr6:145734762-145734994 | Common:3; Rare:88 |