Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:135034166-135034293 | Rare:17 | ||||
chr6:135956654-135956691 | Rare:5 | ||||
chr6:136367104-136367129 | Rare:3 | ||||
chr6:136375650-136375830 | Rare:33 | ||||
chr6:136527853-136528158 | Rare:40 | ||||
chr6:142374586-142374628 | Rare:7 | ||||
chr6:142446198-142446492 | Rare:46 | ||||
chr6:143862011-143862183 | Common:1; Rare:47 | ||||
chr6:144094883-144094997 | Common:1; Rare:25 | ||||
chr6:145650379-145650446 | Rare:13 | ||||
chr6:149317488-149317553 | Rare:15 | ||||
chr6:149879458-149879556 | Rare:9 | ||||
chr6:152151344-152151593 | Common:3; Rare:48; Clinvar:1; Clinvar (benign):1 | ||||
chr6:152306196-152306431 | Common:3; Rare:52 | ||||
chr6:152324567-152324787 | Common:2; Rare:63 |