| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:151240213-151240410 | Common:2; Rare:52 | ||||
| chr6:151452023-151452573 | Common:5; Rare:199; Clinvar (benign):3 | ||||
| chr6:152302032-152302206 | Rare:50; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:152982960-152983296 | Common:2; Rare:107 | ||||
| chr6:152983465-152983784 | Common:4; Rare:114 | ||||
| chr6:153002681-153002888 | Common:3; Rare:70 | ||||
| chr6:153131211-153131501 | Rare:128 | ||||
| chr6:154733216-154733434 | Rare:87 | ||||
| chr6:155314436-155314817 | Common:11; Rare:135 | ||||
| chr6:157323497-157323652 | Common:3; Rare:47 | ||||
| chr6:158168170-158168402 | Common:3; Rare:89; Clinvar:1 | ||||
| chr6:158536331-158536741 | Common:2; Rare:167 | ||||
| chr6:158642180-158642507 | Rare:59 | ||||
| chr6:158644654-158645013 | Common:3; Rare:133 | ||||
| chr6:158818226-158818354 | Common:2; Rare:49 |