Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:8878578-8878843 | Rare:136 | ||||
chr1:9749606-9749855 | Rare:79 | ||||
chr1:9942898-9943133 | Common:2; Rare:60 | ||||
chr1:9943219-9943492 | Common:3; Rare:69 | ||||
chr1:10398720-10399126 | Common:2; Rare:149 | ||||
chr1:10415131-10415282 | Rare:30 | ||||
chr1:10430694-10430802 | Common:3; Rare:28 | ||||
chr1:10472441-10472628 | Rare:53 | ||||
chr1:11012249-11012447 | Rare:50 | ||||
chr1:11059979-11060319 | Common:3; Rare:107 | ||||
chr1:11099817-11099910 | Rare:41 | ||||
chr1:11262495-11262796 | Common:2; Rare:90 | ||||
chr1:11272951-11273280 | Rare:92; Clinvar:1; Clinvar (benign):1 | ||||
chr1:11654351-11654499 | Rare:42 | ||||
chr1:11654669-11654909 | Common:4; Rare:68 |