Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:92298945-92299074 | Common:1; Rare:64; Clinvar:1; Clinvar (benign):1 | ||||
chr1:92483762-92483799 | Common:1; Rare:6 | ||||
chr1:92483952-92484111 | Rare:23 | ||||
chr1:92485914-92486198 | Common:1; Rare:59 | ||||
chr1:92832282-92832448 | Rare:53 | ||||
chr1:92832545-92832865 | Rare:89 | ||||
chr1:92835943-92836337 | Common:1; Rare:79; Clinvar:1; Clinvar (benign):4 | ||||
chr1:92961408-92961590 | Rare:70 | ||||
chr1:93079097-93079428 | Common:3; Rare:122 | ||||
chr1:93179886-93179961 | Common:1; Rare:18 | ||||
chr1:93180053-93180270 | Rare:80 | ||||
chr1:93180291-93180773 | Common:2; Rare:195 | ||||
chr1:93181118-93181337 | Common:1; Rare:37 | ||||
chr1:93345738-93345962 | Common:4; Rare:85 | ||||
chr1:93448023-93448144 | Common:1; Rare:45 |