Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23800729-23800965 | Common:1; Rare:86 | ||||
chr1:23825398-23825534 | Common:2; Rare:48; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:23959056-23959297 | Common:3; Rare:44 | ||||
chr1:23959641-23959922 | Common:2; Rare:74 | ||||
chr1:23980189-23980497 | Rare:79 | ||||
chr1:24413502-24413564 | Rare:10 | ||||
chr1:24413691-24413914 | Common:1; Rare:53 | ||||
chr1:24415633-24415889 | Common:1; Rare:63 | ||||
chr1:24502292-24502568 | Common:1; Rare:68 | ||||
chr1:24502739-24503099 | Common:2; Rare:104 | ||||
chr1:24556022-24556149 | Common:2; Rare:37 | ||||
chr1:24642882-24643343 | Common:2; Rare:152 | ||||
chr1:25232159-25232657 | Common:1; Rare:165 | ||||
chr1:25246927-25247132 | Rare:76 | ||||
chr1:25247318-25247756 | Common:4; Rare:154 |