| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:148826431-148826623 | Common:2; Rare:52 | ||||
| chr5:150585883-150586026 | Common:4; Rare:28 | ||||
| chr5:150778474-150778845 | Common:5; Rare:119 | ||||
| chr5:150946520-150946607 | Rare:21 | ||||
| chr5:151027614-151028047 | Common:2; Rare:109 | ||||
| chr5:151700465-151700582 | Rare:16 | ||||
| chr5:154682943-154683002 | Rare:23 | ||||
| chr5:154799731-154799987 | Common:2; Rare:69 | ||||
| chr5:159100301-159100700 | Common:4; Rare:122 | ||||
| chr5:164296667-164296976 | Rare:73 | ||||
| chr5:170199134-170199392 | Common:2; Rare:48 | ||||
| chr5:172700289-172700475 | Common:2; Rare:40 | ||||
| chr5:173719688-173719914 | Common:2; Rare:55 | ||||
| chr5:177385934-177386248 | Common:1; Rare:123; Clinvar:2; Clinvar (benign):4 | ||||
| chr5:177396839-177397033 | Rare:73; Clinvar:1; Clinvar (benign):1 |