| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:5261229-5261635 | Common:20; Rare:208 | ||||
| chr6:7107607-7108025 | Common:2; Rare:242 | ||||
| chr6:7108415-7108665 | Common:2; Rare:120 | ||||
| chr6:7108753-7108914 | Common:3; Rare:66 | ||||
| chr6:7312480-7312940 | Common:4; Rare:180 | ||||
| chr6:7313051-7313386 | Common:10; Rare:248 | ||||
| chr6:7347347-7347747 | Common:16; Rare:149 | ||||
| chr6:7389230-7389480 | Common:1; Rare:91 | ||||
| chr6:7389730-7389904 | Common:2; Rare:98 | ||||
| chr6:7541178-7542079 | Common:10; Rare:454; Clinvar:19; Clinvar (benign):13; Clinvar (pathogenic):1 | ||||
| chr6:7909710-7910290 | Common:11; Rare:239 | ||||
| chr6:7910506-7910935 | Common:8; Rare:277 | ||||
| chr6:8064290-8064640 | Common:8; Rare:211 | ||||
| chr6:8102511-8102785 | Common:3; Rare:165 | ||||
| chr6:8435314-8435721 | Common:14; Rare:250 |