Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:48989728-48989912 | Rare:49 | ||||
chr3:49007086-49007434 | Common:2; Rare:136 | ||||
chr3:49021502-49021720 | Rare:55; Clinvar:1 | ||||
chr3:49029319-49029564 | Common:2; Rare:168 | ||||
chr3:49093573-49093643 | Rare:34 | ||||
chr3:49104726-49104910 | Rare:77; Clinvar (benign):3 | ||||
chr3:49120754-49120861 | Rare:33 | ||||
chr3:49132790-49133161 | Rare:83; Clinvar:3 | ||||
chr3:49166294-49166437 | Common:1; Rare:35 | ||||
chr3:49340013-49340127 | Common:2; Rare:53 | ||||
chr3:49358025-49358393 | Common:4; Rare:191 | ||||
chr3:49411820-49412423 | Common:2; Rare:208 | ||||
chr3:49429255-49429485 | Common:1; Rare:51 | ||||
chr3:49469986-49470325 | Common:1; Rare:105 | ||||
chr3:49674225-49674402 | Common:1; Rare:70 |