Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:113255700-113256010 | Common:4; Rare:92 | ||||
chr1:113280150-113280560 | Common:2; Rare:64 | ||||
chr1:113388748-113389056 | Common:1; Rare:77 | ||||
chr1:113555336-113555736 | Common:1; Rare:92 | ||||
chr1:113692691-113694087 | Common:7; Rare:372 | ||||
chr1:113694127-113695042 | Common:6; Rare:248 | ||||
chr1:113702340-113702740 | Common:4; Rare:115 | ||||
chr1:113791107-113792125 | Common:8; Rare:218 | ||||
chr1:113808253-113809635 | Common:3; Rare:477 | ||||
chr1:113809820-113810320 | Common:3; Rare:185 | ||||
chr1:113811115-113811498 | Rare:95 | ||||
chr1:113898564-113899292 | Rare:209; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr1:114033110-114033650 | Common:7; Rare:172 | ||||
chr1:114034078-114034436 | Common:8; Rare:120 | ||||
chr1:114113798-114114781 | Common:7; Rare:262 |