Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:239711815-239711865 | Rare:8 | ||||
chr1:239730425-239730594 | Rare:27 | ||||
chr1:243488986-243489282 | Rare:83; Clinvar (benign):2 | ||||
chr1:244451138-244451257 | Common:2; Rare:34 | ||||
chr1:244662148-244662340 | Rare:32 | ||||
chr1:244837358-244837635 | Common:2; Rare:56 | ||||
chr1:244863661-244863887 | Rare:79; Clinvar:3; Clinvar (benign):4 | ||||
chr1:244863889-244863924 | Rare:12; Clinvar (benign):1 | ||||
chr1:246890008-246890275 | Common:3; Rare:52 | ||||
chr1:247132019-247132097 | Rare:15 | ||||
chr1:247132652-247132992 | Common:3; Rare:71 | ||||
chr1:247133032-247133313 | Common:1; Rare:47 | ||||
chr1:247134235-247134275 | Rare:1 | ||||
chr1:247140621-247140633 | |||||
chr1:247159703-247160023 | Common:6; Rare:95 |