| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:45421910-45422340 | Common:3; Rare:166 | ||||
| chr6:46652706-46653031 | Rare:136 | ||||
| chr6:47477691-47477991 | Common:3; Rare:116; Clinvar:4; Clinvar (benign):4 | ||||
| chr6:47478065-47478251 | Common:4; Rare:126; Clinvar:3; Clinvar (benign):6 | ||||
| chr6:49463143-49463454 | Common:2; Rare:176; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:52284635-52285132 | Common:5; Rare:301 | ||||
| chr6:52361890-52362330 | Common:5; Rare:162 | ||||
| chr6:52420087-52420386 | Common:6; Rare:245; Clinvar:2; Clinvar (benign):4 | ||||
| chr6:52576951-52577309 | Common:11; Rare:195 | ||||
| chr6:52670967-52671225 | Rare:105 | ||||
| chr6:52995263-52995616 | Common:8; Rare:270 | ||||
| chr6:53064758-53064961 | Rare:51 | ||||
| chr6:53065337-53065525 | Common:2; Rare:108 | ||||
| chr6:53348764-53349224 | Common:5; Rare:309 | ||||
| chr6:53794550-53794730 | Common:2; Rare:56 |