Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:19210251-19210395 | Rare:55 | ||||
chr1:19251510-19251866 | Common:6; Rare:116 | ||||
chr1:19311988-19312333 | Common:8; Rare:163 | ||||
chr1:19485439-19485743 | Common:1; Rare:105 | ||||
chr1:20508063-20508236 | Common:2; Rare:62 | ||||
chr1:20661230-20661245 | Rare:5 | ||||
chr1:20661346-20661702 | Common:3; Rare:128; Clinvar:4; Clinvar (benign):6 | ||||
chr1:20787253-20787447 | Rare:91 | ||||
chr1:21345459-21345674 | Common:2; Rare:80 | ||||
chr1:23559414-23559643 | Common:1; Rare:99 | ||||
chr1:23559645-23559671 | Common:1; Rare:12 | ||||
chr1:23791075-23791231 | Rare:45 | ||||
chr1:23825411-23825543 | Common:2; Rare:43; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:23959046-23959287 | Common:3; Rare:46 | ||||
chr1:23959608-23959870 | Common:2; Rare:72 |