Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:19311972-19312350 | Common:8; Rare:171 | ||||
chr1:19485451-19485749 | Rare:105 | ||||
chr1:19596835-19597102 | Common:2; Rare:113 | ||||
chr1:19799864-19800046 | Common:4; Rare:63 | ||||
chr1:20508063-20508194 | Common:2; Rare:49 | ||||
chr1:20652626-20652925 | Common:1; Rare:72; Clinvar:2; Clinvar (benign):2 | ||||
chr1:20661230-20661286 | Common:1; Rare:20; Clinvar:1; Clinvar (benign):1 | ||||
chr1:20661340-20661730 | Common:3; Rare:140; Clinvar:4; Clinvar (benign):6 | ||||
chr1:20786594-20786849 | Rare:96 | ||||
chr1:20787196-20787517 | Rare:154 | ||||
chr1:21176839-21177113 | Rare:81 | ||||
chr1:21290201-21290371 | Rare:34 | ||||
chr1:21345454-21345685 | Common:2; Rare:85 | ||||
chr1:21782990-21783291 | Common:2; Rare:108 | ||||
chr1:22052555-22052736 | Common:2; Rare:60 |