Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:40692022-40692333 | Common:3; Rare:152 | ||||
chr1:40862202-40862628 | Common:10; Rare:252 | ||||
chr1:40979588-40979816 | Common:6; Rare:150 | ||||
chr1:40979891-40980082 | Rare:109 | ||||
chr1:41242077-41242480 | Common:1; Rare:183 | ||||
chr1:42335116-42335395 | Common:11; Rare:242 | ||||
chr1:42335638-42336230 | Common:7; Rare:139 | ||||
chr1:42456120-42456600 | Common:2; Rare:239 | ||||
chr1:42463018-42463329 | Common:4; Rare:93 | ||||
chr1:42658265-42658725 | Common:5; Rare:167 | ||||
chr1:42682129-42682591 | Common:4; Rare:247 | ||||
chr1:42766970-42767309 | Common:8; Rare:223; Clinvar (benign):2 | ||||
chr1:42816961-42817141 | Common:2; Rare:84 | ||||
chr1:42817250-42817546 | Rare:142 | ||||
chr1:42846384-42846666 | Common:2; Rare:156 |