| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:138572426-138572723 | Common:2; Rare:60 | ||||
| chr6:138692173-138692503 | Common:1; Rare:139 | ||||
| chr6:138773290-138773580 | Common:7; Rare:215 | ||||
| chr6:138773646-138773825 | Common:6; Rare:154 | ||||
| chr6:138987870-138988836 | Common:14; Rare:338 | ||||
| chr6:142147187-142147300 | Rare:92 | ||||
| chr6:142301738-142302701 | Common:18; Rare:470 | ||||
| chr6:142944587-142944726 | Rare:63 | ||||
| chr6:142944989-142945307 | Common:2; Rare:153 | ||||
| chr6:143060160-143060530 | Common:3; Rare:123 | ||||
| chr6:143060700-143060990 | Common:15; Rare:191 | ||||
| chr6:143450595-143450965 | Common:2; Rare:244; Clinvar:8; Clinvar (benign):2 | ||||
| chr6:143511544-143511813 | Common:8; Rare:119 | ||||
| chr6:143536781-143536938 | Rare:68 | ||||
| chr6:143843168-143843483 | Common:4; Rare:203 |