Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:178153818-178154103 | Rare:87; Clinvar:4; Clinvar (benign):1 | ||||
chr5:178940999-178941233 | Common:1; Rare:63 | ||||
chr5:179559503-179559781 | Common:1; Rare:86 | ||||
chr5:179623624-179623980 | Common:4; Rare:129 | ||||
chr5:179698661-179699091 | Common:4; Rare:141 | ||||
chr5:179858792-179858993 | Rare:111 | ||||
chr5:179907842-179908021 | Common:2; Rare:96 | ||||
chr5:180810102-180810216 | Common:1; Rare:23 | ||||
chr5:181223118-181223313 | Rare:66 | ||||
chr5:181223645-181223750 | Common:3; Rare:27 | ||||
chr5:181243690-181243875 | Common:2; Rare:58 | ||||
chr5:181261054-181261286 | Rare:79 | ||||
chr6:292450-292533 | Rare:26 | ||||
chr6:2245445-2245747 | Common:1; Rare:103 | ||||
chr6:2971533-2971913 | Common:2; Rare:96 |