| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:183472917-183473047 | Common:2; Rare:30 | ||||
| chr1:183589960-183590174 | Common:1; Rare:48; Clinvar (benign):1 | ||||
| chr1:183590359-183590599 | Common:3; Rare:60; Clinvar (benign):2 | ||||
| chr1:183590624-183590717 | Common:1; Rare:12 | ||||
| chr1:183590863-183591205 | Common:4; Rare:57 | ||||
| chr1:183633803-183634030 | Common:4; Rare:39 | ||||
| chr1:183635633-183636271 | Common:5; Rare:162 | ||||
| chr1:183805079-183805272 | Rare:62 | ||||
| chr1:184051483-184051888 | Common:4; Rare:127 | ||||
| chr1:184051943-184052078 | Common:1; Rare:37 | ||||
| chr1:184052082-184052164 | Rare:17 | ||||
| chr1:184754179-184754411 | Common:2; Rare:56 | ||||
| chr1:184754736-184755298 | Common:1; Rare:135 | ||||
| chr1:184973969-184974077 | Common:1; Rare:24 | ||||
| chr1:184974357-184974597 | Rare:63 |