Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:113904783-113905450 | Common:7; Rare:193; Clinvar (benign):1 | ||||
chr1:113929515-113929618 | Common:1; Rare:25 | ||||
chr1:114510779-114511141 | Common:2; Rare:130 | ||||
chr1:114511193-114511330 | Common:3; Rare:50 | ||||
chr1:114581577-114581839 | Common:1; Rare:115 | ||||
chr1:114669991-114670255 | Common:1; Rare:83 | ||||
chr1:115089455-115089600 | Common:2; Rare:54 | ||||
chr1:115976440-115976571 | Rare:46 | ||||
chr1:116373083-116373530 | Common:3; Rare:146 | ||||
chr1:116374065-116374304 | Rare:72 | ||||
chr1:116387834-116388259 | Common:1; Rare:80 | ||||
chr1:116398610-116399084 | Common:1; Rare:91 | ||||
chr1:116399169-116399553 | Rare:64 | ||||
chr1:116400846-116401204 | Rare:74; Clinvar (pathogenic):1 | ||||
chr1:116667668-116667895 | Common:2; Rare:82 |