| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:136250210-136250640 | Common:6; Rare:215 | ||||
| chr6:136289746-136290068 | Common:4; Rare:270 | ||||
| chr6:136550294-136550665 | Common:4; Rare:219 | ||||
| chr6:136792240-136792740 | Common:8; Rare:221 | ||||
| chr6:136793002-136793312 | Common:1; Rare:81 | ||||
| chr6:136822441-136822622 | Common:7; Rare:97; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr6:137219323-137219509 | Common:6; Rare:112; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr6:137866770-137867290 | Common:1; Rare:203 | ||||
| chr6:138107400-138107584 | Common:4; Rare:90 | ||||
| chr6:138161867-138162012 | Common:4; Rare:48 | ||||
| chr6:138404122-138404389 | Common:6; Rare:157 | ||||
| chr6:138773642-138773858 | Common:4; Rare:162 | ||||
| chr6:138987929-138988090 | Common:2; Rare:37 | ||||
| chr6:138988207-138988431 | Common:3; Rare:61 | ||||
| chr6:139028500-139028790 | Common:1; Rare:58 |