Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:173056145-173056407 | Common:1; Rare:73 | ||||
chr5:173144427-173144548 | Rare:29 | ||||
chr5:173328266-173328377 | Common:1; Rare:26 | ||||
chr5:173328411-173328605 | Rare:36 | ||||
chr5:176388543-176388806 | Common:4; Rare:102 | ||||
chr5:177022642-177022741 | Rare:37 | ||||
chr5:177351650-177351968 | Rare:78 | ||||
chr5:178153827-178154110 | Rare:83; Clinvar:3; Clinvar (benign):1 | ||||
chr5:179559560-179559781 | Common:1; Rare:62 | ||||
chr5:179698595-179699092 | Common:4; Rare:176 | ||||
chr5:179858797-179858958 | Rare:91 | ||||
chr5:180353281-180353490 | Common:9; Rare:93 | ||||
chr5:180810126-180810223 | Rare:20 | ||||
chr5:180861236-180861391 | Common:2; Rare:61 | ||||
chr5:181223118-181223309 | Rare:64 |