Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:214280935-214281267 | Common:3; Rare:136 | ||||
chr1:214602906-214603493 | Common:5; Rare:156 | ||||
chr1:216723420-216723636 | Rare:58 | ||||
chr1:217089587-217089940 | Common:1; Rare:76 | ||||
chr1:217630980-217631385 | Common:4; Rare:119 | ||||
chr1:218285178-218285385 | Common:3; Rare:94 | ||||
chr1:219173749-219173911 | Common:1; Rare:85 | ||||
chr1:219174157-219174171 | Rare:3 | ||||
chr1:220046401-220046742 | Common:1; Rare:107 | ||||
chr1:220093889-220094256 | Common:12; Rare:120; Clinvar (benign):2 | ||||
chr1:220272345-220272576 | Rare:63; Clinvar:5 | ||||
chr1:221742065-221742372 | Common:1; Rare:85 | ||||
chr1:222589774-222590039 | Common:2; Rare:75 | ||||
chr1:222617783-222618126 | Common:3; Rare:87 | ||||
chr1:222644094-222644419 | Common:3; Rare:98 |