| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:142301841-142302159 | Common:6; Rare:92 | ||||
| chr6:142302177-142302698 | Common:1; Rare:122 | ||||
| chr6:143060700-143060983 | Common:8; Rare:99 | ||||
| chr6:143450651-143450998 | Common:1; Rare:120; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:143511651-143511769 | Common:4; Rare:28 | ||||
| chr6:144095493-144095840 | Common:6; Rare:101 | ||||
| chr6:144285130-144285650 | Common:3; Rare:141 | ||||
| chr6:145814655-145814950 | Common:1; Rare:131 | ||||
| chr6:145964035-145964130 | Common:4; Rare:22 | ||||
| chr6:149546001-149546153 | Rare:63 | ||||
| chr6:149746491-149746643 | Common:2; Rare:75 | ||||
| chr6:149749547-149749800 | Rare:115 | ||||
| chr6:151325454-151325770 | Common:2; Rare:72 | ||||
| chr6:151391516-151391842 | Common:3; Rare:87 | ||||
| chr6:151452029-151452548 | Common:4; Rare:183 |