| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:31821962-31822281 | Common:4; Rare:101 | ||||
| chr6:31826915-31827046 | Rare:45 | ||||
| chr6:32083020-32083400 | Rare:104 | ||||
| chr6:32894050-32894470 | Common:6; Rare:141 | ||||
| chr6:32894573-32894836 | Common:14; Rare:128 | ||||
| chr6:33249150-33249624 | Common:4; Rare:260 | ||||
| chr6:33301550-33302201 | Common:12; Rare:171 | ||||
| chr6:33397801-33398340 | Common:5; Rare:246 | ||||
| chr6:33425550-33425901 | Common:3; Rare:136; Clinvar:2; Clinvar (benign):4 | ||||
| chr6:33571201-33571601 | Common:2; Rare:110 | ||||
| chr6:33590270-33591250 | Common:15; Rare:272 | ||||
| chr6:33787680-33788160 | Common:11; Rare:138 | ||||
| chr6:33840440-33840751 | Rare:93 | ||||
| chr6:34223880-34224230 | Common:10; Rare:165 | ||||
| chr6:34341840-34342280 | Common:2; Rare:167 |