Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:33818013-33818140 | Common:1; Rare:47 | ||||
chr13:41061401-41061558 | Common:2; Rare:45 | ||||
chr13:42992184-42992398 | Common:3; Rare:45 | ||||
chr13:44436809-44437055 | Common:2; Rare:78 | ||||
chr13:44989449-44989607 | Rare:58 | ||||
chr13:45341073-45341508 | Common:4; Rare:217 | ||||
chr13:49247823-49247967 | Rare:43 | ||||
chr13:50081980-50082223 | Common:1; Rare:66 | ||||
chr13:51804160-51804296 | Rare:35 | ||||
chr13:52455301-52455501 | Common:3; Rare:62 | ||||
chr13:72727595-72727950 | Common:4; Rare:131 | ||||
chr13:72781896-72782156 | Common:1; Rare:95 | ||||
chr13:95676828-95677172 | Common:2; Rare:132 | ||||
chr13:97222062-97222356 | Rare:51 | ||||
chr13:100088941-100089111 | Rare:62; Clinvar:1; Clinvar (benign):2 |