Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:212699541-212700232 | Common:13; Rare:267 | ||||
chr1:212791716-212792008 | Common:6; Rare:138 | ||||
chr1:212792075-212792520 | Common:11; Rare:107 | ||||
chr1:212857510-212857920 | Common:5; Rare:69 | ||||
chr1:212858059-212858283 | Common:4; Rare:58; Clinvar:1 | ||||
chr1:212858781-212859181 | Rare:237; Clinvar:12; Clinvar (pathogenic):5 | ||||
chr1:212950337-212950609 | Common:2; Rare:62 | ||||
chr1:213015217-213015632 | Rare:107 | ||||
chr1:213015638-213015928 | Rare:91 | ||||
chr1:213051139-213051351 | Common:1; Rare:68 | ||||
chr1:213982591-213982849 | Common:1; Rare:76 | ||||
chr1:213987633-213988031 | Rare:82 | ||||
chr1:213988194-213988536 | Common:4; Rare:98 | ||||
chr1:214280725-214281188 | Common:3; Rare:171 | ||||
chr1:214281403-214281602 | Common:3; Rare:103 |