Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:213987714-213987973 | Rare:50 | ||||
chr1:214280972-214281222 | Common:2; Rare:109 | ||||
chr1:214603037-214603321 | Common:3; Rare:77 | ||||
chr1:217631013-217631341 | Common:2; Rare:84 | ||||
chr1:218285202-218285350 | Common:2; Rare:71 | ||||
chr1:218345764-218346078 | Common:4; Rare:92; Clinvar:8; Clinvar (benign):3 | ||||
chr1:218346736-218346932 | Rare:50; Clinvar:7; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:219173771-219173906 | Common:1; Rare:73 | ||||
chr1:220093902-220094246 | Common:12; Rare:114; Clinvar (benign):2 | ||||
chr1:220272351-220272548 | Rare:56; Clinvar:5 | ||||
chr1:221742054-221742288 | Rare:61 | ||||
chr1:222548061-222548192 | Rare:30 | ||||
chr1:222589755-222589978 | Common:2; Rare:67 | ||||
chr1:222617856-222618127 | Common:3; Rare:71 | ||||
chr1:222644094-222644386 | Common:3; Rare:86 |