Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:24415600-24415879 | Common:2; Rare:69 | ||||
chr1:24502765-24503122 | Common:2; Rare:97 | ||||
chr1:24642966-24643329 | Common:2; Rare:114 | ||||
chr1:25232159-25232587 | Common:1; Rare:136 | ||||
chr1:25246894-25247146 | Common:1; Rare:97 | ||||
chr1:25247331-25247527 | Rare:82 | ||||
chr1:25337828-25337946 | Rare:14 | ||||
chr1:25338177-25338447 | Common:1; Rare:95 | ||||
chr1:25819885-25820029 | Common:3; Rare:44 | ||||
chr1:26110905-26111209 | Common:3; Rare:92 | ||||
chr1:26279923-26280203 | Rare:152 | ||||
chr1:26317676-26317958 | Common:3; Rare:47 | ||||
chr1:26432091-26432446 | Common:5; Rare:93; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26472298-26472551 | Common:4; Rare:92 | ||||
chr1:26472929-26473285 | Common:1; Rare:166 |