Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:49104720-49104948 | Rare:92; Clinvar:1; Clinvar (benign):4 | ||||
chr3:49120767-49120841 | Rare:21 | ||||
chr3:49132985-49133161 | Rare:37; Clinvar:1 | ||||
chr3:49166294-49166437 | Common:1; Rare:35 | ||||
chr3:49171518-49171636 | Common:2; Rare:29 | ||||
chr3:49340020-49340112 | Common:2; Rare:44 | ||||
chr3:49411909-49412423 | Common:2; Rare:191 | ||||
chr3:49469983-49470325 | Common:1; Rare:108 | ||||
chr3:49674225-49674395 | Common:1; Rare:64 | ||||
chr3:49688671-49688777 | Common:2; Rare:28 | ||||
chr3:49689461-49689606 | Rare:46 | ||||
chr3:49723887-49724193 | Common:9; Rare:101 | ||||
chr3:49929759-49929849 | Rare:37 | ||||
chr3:50292343-50292659 | Common:1; Rare:140 | ||||
chr3:50299355-50299695 | Common:1; Rare:86 |