Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:45341071-45341515 | Common:4; Rare:224 | ||||
chr13:46052693-46052819 | Common:2; Rare:38 | ||||
chr13:46797122-46797326 | Common:3; Rare:75 | ||||
chr13:48001263-48001405 | Common:1; Rare:66; Clinvar:3; Clinvar (benign):2 | ||||
chr13:48303700-48304032 | Common:1; Rare:105; Clinvar:15; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
chr13:49247811-49247982 | Rare:50 | ||||
chr13:49443995-49444373 | Common:1; Rare:122 | ||||
chr13:49936296-49936561 | Rare:74 | ||||
chr13:50081980-50082264 | Common:1; Rare:79 | ||||
chr13:51453029-51453388 | Rare:140 | ||||
chr13:51804113-51804227 | Common:2; Rare:36 | ||||
chr13:52012130-52012428 | Common:2; Rare:96; Clinvar:1 | ||||
chr13:52450572-52450788 | Rare:63 | ||||
chr13:52455344-52455607 | Common:3; Rare:101 | ||||
chr13:52653109-52653183 | Common:1; Rare:26 |