Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:19251471-19252024 | Common:16; Rare:326 | ||||
chr1:19312035-19312384 | Common:16; Rare:308 | ||||
chr1:19385820-19386180 | Rare:141 | ||||
chr1:19484758-19484893 | Rare:34 | ||||
chr1:19485403-19485810 | Common:1; Rare:289 | ||||
chr1:19596767-19597091 | Common:5; Rare:233 | ||||
chr1:19644161-19644392 | Common:5; Rare:113 | ||||
chr1:19799900-19800239 | Common:6; Rare:123 | ||||
chr1:19980414-19980592 | Common:2; Rare:39 | ||||
chr1:20485760-20486630 | Common:2; Rare:316 | ||||
chr1:20486648-20486846 | Common:2; Rare:105 | ||||
chr1:20508036-20508240 | Common:4; Rare:129 | ||||
chr1:20552060-20552590 | Common:2; Rare:145 | ||||
chr1:20633293-20633524 | Rare:118 | ||||
chr1:20661340-20661736 | Common:6; Rare:269; Clinvar:8; Clinvar (benign):12 |