Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:16155998-16156172 | Rare:40; Clinvar:2 | ||||
chr1:16352420-16352615 | Common:3; Rare:102 | ||||
chr1:16440538-16440774 | Common:1; Rare:69 | ||||
chr1:16613436-16613660 | Common:2 | ||||
chr1:17053947-17054239 | Common:3; Rare:94; Clinvar:16; Clinvar (benign):12 | ||||
chr1:17439652-17439892 | Rare:80 | ||||
chr1:17618247-17618402 | Common:2; Rare:33 | ||||
chr1:18902519-18902796 | Common:2; Rare:87; Clinvar:9 | ||||
chr1:19210223-19210523 | Rare:102 | ||||
chr1:19251494-19251902 | Common:8; Rare:144 | ||||
chr1:19312008-19312346 | Common:8; Rare:160 | ||||
chr1:19485448-19485749 | Rare:106 | ||||
chr1:19596790-19597108 | Common:3; Rare:125 | ||||
chr1:20508045-20508229 | Common:2; Rare:66 | ||||
chr1:20661340-20661736 | Common:3; Rare:143; Clinvar:4; Clinvar (benign):6 |