Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:94820190-94820480 | Common:3; Rare:81 | ||||
chr1:95072852-95073030 | Common:2; Rare:122; Clinvar (benign):2 | ||||
chr1:95116650-95116930 | Rare:77 | ||||
chr1:95117231-95117435 | Rare:118 | ||||
chr1:95233976-95234239 | Common:8; Rare:159 | ||||
chr1:96721600-96721862 | Common:3; Rare:182 | ||||
chr1:97920902-97921152 | Rare:173; Clinvar:6; Clinvar (pathogenic):1 | ||||
chr1:99766607-99766722 | Rare:22 | ||||
chr1:99849997-99850190 | Common:1; Rare:123 | ||||
chr1:99850200-99850520 | Rare:141; Clinvar:6; Clinvar (benign):4 | ||||
chr1:99969899-99970190 | Common:3; Rare:119 | ||||
chr1:99970277-99970560 | Rare:117 | ||||
chr1:100037972-100038203 | Common:2; Rare:178 | ||||
chr1:100132876-100133235 | Common:5; Rare:247 | ||||
chr1:100133250-100133490 | Common:5; Rare:141 |