Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:17011907-17012138 | Common:2; Rare:65 | ||||
chr1:17053966-17054399 | Common:3; Rare:131; Clinvar:16; Clinvar (benign):10 | ||||
chr1:17348422-17348623 | Common:2; Rare:25 | ||||
chr1:17438031-17438152 | Common:1; Rare:47 | ||||
chr1:17438377-17438577 | Common:3; Rare:70 | ||||
chr1:17438620-17438910 | Common:3; Rare:101 | ||||
chr1:17439248-17439293 | Common:1; Rare:15 | ||||
chr1:17439634-17440381 | Rare:194 | ||||
chr1:17539640-17539883 | Rare:60 | ||||
chr1:17539896-17540031 | Common:1; Rare:27 | ||||
chr1:17540175-17540469 | Common:3; Rare:58 | ||||
chr1:18902124-18902153 | Rare:6 | ||||
chr1:18902394-18903040 | Common:10; Rare:175; Clinvar:9; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:18955392-18955740 | Common:2; Rare:66 | ||||
chr1:18955820-18955971 | Rare:37 |