| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:214550750-214551517 | Common:12; Rare:290 | ||||
| chr1:214551571-214552053 | Common:2; Rare:144 | ||||
| chr1:214552334-214552567 | Common:3; Rare:38 | ||||
| chr1:214602902-214603291 | Common:3; Rare:111 | ||||
| chr1:215082777-215083399 | Common:6; Rare:317 | ||||
| chr1:215083630-215084030 | Rare:83 | ||||
| chr1:215567264-215567386 | Rare:25 | ||||
| chr1:215567880-215568240 | Common:1; Rare:73 | ||||
| chr1:216723369-216723640 | Rare:77 | ||||
| chr1:216805227-216805627 | Common:8; Rare:77 | ||||
| chr1:217631015-217631414 | Common:3; Rare:119 | ||||
| chr1:218285094-218285389 | Common:5; Rare:118 | ||||
| chr1:218345952-218346105 | Common:5; Rare:53; Clinvar:8; Clinvar (benign):3 | ||||
| chr1:218346119-218346322 | Rare:32; Clinvar:1 | ||||
| chr1:218346699-218347099 | Rare:134; Clinvar:16; Clinvar (benign):6; Clinvar (pathogenic):2 |