Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23799516-23799702 | Rare:29 | ||||
chr1:23800723-23800959 | Common:1; Rare:84 | ||||
chr1:23825411-23825565 | Common:2; Rare:46; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:23959090-23959304 | Common:3; Rare:41 | ||||
chr1:23959641-23959870 | Common:2; Rare:64 | ||||
chr1:23980196-23980455 | Rare:70 | ||||
chr1:23980465-23980495 | Rare:6 | ||||
chr1:24413691-24413897 | Common:1; Rare:46 | ||||
chr1:24642890-24643335 | Common:2; Rare:147 | ||||
chr1:25232442-25232662 | Rare:89 | ||||
chr1:25247042-25247133 | Rare:29 | ||||
chr1:25247419-25247673 | Common:3; Rare:101 | ||||
chr1:25338214-25338437 | Common:1; Rare:78 | ||||
chr1:25819866-25820024 | Common:3; Rare:51 | ||||
chr1:25859351-25859580 | Common:3; Rare:97 |