Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:2391470-2391943 | Common:2; Rare:166 | ||||
chr1:2412454-2412850 | Common:2; Rare:166; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
chr1:2413000-2413119 | Rare:32 | ||||
chr1:2413309-2413324 | Rare:4 | ||||
chr1:2413325-2413338 | Rare:5 | ||||
chr1:2413789-2413837 | Rare:11 | ||||
chr1:2526219-2526448 | Common:1; Rare:83 | ||||
chr1:2526500-2526759 | Common:4; Rare:99 | ||||
chr1:2526981-2527053 | Rare:15 | ||||
chr1:2555622-2555837 | Common:3; Rare:55 | ||||
chr1:2555971-2556259 | Common:1; Rare:79 | ||||
chr1:2556337-2556670 | Common:1; Rare:127 | ||||
chr1:2556777-2556813 | Rare:4 | ||||
chr1:2556947-2557137 | Common:3; Rare:40 | ||||
chr1:2586415-2586528 | Rare:22 |