Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:43120066-43120164 | Common:3; Rare:34 | ||||
chr1:44776329-44776492 | Rare:34 | ||||
chr1:46037270-46037510 | Common:1; Rare:57 | ||||
chr1:46900439-46900578 | Common:1; Rare:37 | ||||
chr1:51326930-51327098 | Rare:38 | ||||
chr1:51518097-51518299 | Rare:47 | ||||
chr1:51790964-51791254 | Common:1; Rare:70 | ||||
chr1:54205181-54205358 | Rare:53 | ||||
chr1:55580820-55581125 | Common:2; Rare:54 | ||||
chr1:58572805-58572880 | Common:1; Rare:4 | ||||
chr1:58575420-58575587 | Common:1; Rare:27; Clinvar:3; Clinvar (benign):1 | ||||
chr1:58575648-58575866 | Common:1; Rare:33; Clinvar:1; Clinvar (benign):1 | ||||
chr1:58576012-58576123 | Common:1; Rare:18; Clinvar:1; Clinvar (benign):2 | ||||
chr1:58781941-58782246 | Rare:91 | ||||
chr1:58782250-58782543 | Common:1; Rare:93; Clinvar:1 |