Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:40161272-40161402 | Rare:33 | ||||
chr1:40257903-40258255 | Common:4; Rare:91; Clinvar:6 | ||||
chr1:40374545-40374671 | Common:12; Rare:29 | ||||
chr1:40450054-40450145 | Common:1; Rare:35 | ||||
chr1:40508626-40508811 | Common:6; Rare:57 | ||||
chr1:40531502-40531653 | Rare:37 | ||||
chr1:40691504-40691864 | Common:2; Rare:160 | ||||
chr1:40692039-40692343 | Common:1; Rare:91 | ||||
chr1:40709160-40709413 | Rare:58 | ||||
chr1:40979547-40979803 | Common:3; Rare:95 | ||||
chr1:41242106-41242380 | Rare:78 | ||||
chr1:42335095-42335386 | Common:6; Rare:139 | ||||
chr1:42456010-42456387 | Common:1; Rare:98 | ||||
chr1:42456499-42456583 | Rare:41 | ||||
chr1:42456843-42456972 | Common:1; Rare:48; Clinvar (pathogenic):1 |