Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:46131973-46132269 | Rare:70 | ||||
chr1:46132578-46132774 | Common:3; Rare:72 | ||||
chr1:46132833-46133244 | Common:3; Rare:112 | ||||
chr1:46174693-46174854 | Rare:21 | ||||
chr1:46174894-46174953 | Common:2; Rare:10 | ||||
chr1:46198346-46198528 | Common:1; Rare:76; Clinvar:1; Clinvar (benign):1 | ||||
chr1:46303138-46303811 | Common:3; Rare:203 | ||||
chr1:46340673-46340855 | Common:3; Rare:57 | ||||
chr1:46604199-46604443 | Common:1; Rare:64 | ||||
chr1:46718493-46718577 | Common:2; Rare:16 | ||||
chr1:47190029-47190199 | Common:1; Rare:34 | ||||
chr1:47314191-47314514 | Common:3; Rare:73 | ||||
chr1:47333696-47333984 | Common:3; Rare:94 | ||||
chr1:48776717-48776780 | Rare:15 | ||||
chr1:50023866-50024029 | Rare:48 |