Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:84574411-84574553 | Common:1; Rare:45 | ||||
chr1:84690425-84690688 | Rare:82 | ||||
chr1:84997101-84997233 | Common:6; Rare:37 | ||||
chr1:85276328-85276774 | Common:6; Rare:140; Clinvar (benign):2 | ||||
chr1:85578013-85578093 | Common:1; Rare:11 | ||||
chr1:85708304-85708506 | Common:2; Rare:71 | ||||
chr1:86704491-86704613 | Rare:45 | ||||
chr1:86704718-86704971 | Common:3; Rare:88 | ||||
chr1:86914306-86914684 | Common:2; Rare:102 | ||||
chr1:87331611-87331769 | Rare:50 | ||||
chr1:88684110-88684583 | Common:3; Rare:121 | ||||
chr1:88992600-88992854 | Common:3; Rare:61 | ||||
chr1:89065204-89065440 | Common:1; Rare:35 | ||||
chr1:89198869-89199001 | Rare:16 | ||||
chr1:89994981-89995193 | Common:2; Rare:80 |