Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:171741928-171742122 | Common:1; Rare:65 | ||||
chr1:171781392-171781718 | Common:4; Rare:83 | ||||
chr1:173477164-173477472 | Common:3; Rare:111 | ||||
chr1:173714861-173715057 | Common:1; Rare:45 | ||||
chr1:173824304-173824850 | Rare:102; Clinvar:2 | ||||
chr1:173867975-173868236 | Common:1; Rare:89 | ||||
chr1:174999646-175000156 | Common:3; Rare:167 | ||||
chr1:178725098-178725319 | Common:10; Rare:85 | ||||
chr1:179143040-179143235 | Rare:36 | ||||
chr1:179882481-179882816 | Rare:158; Clinvar:7; Clinvar (benign):2 | ||||
chr1:181088494-181088704 | Rare:67 | ||||
chr1:182789598-182789773 | Common:2; Rare:53 | ||||
chr1:182839199-182839394 | Common:1; Rare:84 | ||||
chr1:183186031-183186283 | Common:4; Rare:55; Clinvar:3; Clinvar (benign):3 | ||||
chr1:183635666-183636123 | Common:5; Rare:132 |