| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:31827442-31827753 | Common:2; Rare:93 | ||||
| chr6:31834531-31834639 | Rare:47 | ||||
| chr6:31834782-31835469 | Common:10; Rare:271 | ||||
| chr6:31835579-31835883 | Rare:53 | ||||
| chr6:31837274-31837334 | Rare:22 | ||||
| chr6:31862761-31863161 | Common:3; Rare:108; Clinvar:3; Clinvar (benign):1 | ||||
| chr6:31897154-31897272 | Rare:28 | ||||
| chr6:31897579-31897746 | Rare:40 | ||||
| chr6:31958371-31958562 | Common:1; Rare:49 | ||||
| chr6:31958850-31959340 | Rare:169; Clinvar:8 | ||||
| chr6:31966826-31967117 | Common:1; Rare:71; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr6:32128185-32128488 | Common:3; Rare:82 | ||||
| chr6:32130137-32130451 | Common:3; Rare:49 | ||||
| chr6:32151903-32151943 | Rare:13 | ||||
| chr6:32153319-32153599 | Rare:51 |