| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:185425877-185426029 | Common:2; Rare:53 | ||||
| chr4:189940644-189940983 | Common:10; Rare:124 | ||||
| chr5:218114-218349 | Common:2; Rare:91; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:443074-443275 | Common:10; Rare:90 | ||||
| chr5:612197-612351 | Rare:61 | ||||
| chr5:892520-892947 | Common:5; Rare:131 | ||||
| chr5:1112028-1112153 | Rare:34 | ||||
| chr5:1799771-1799988 | Common:8; Rare:102 | ||||
| chr5:1801283-1801415 | Common:4; Rare:52; Clinvar (benign):1 | ||||
| chr5:6632977-6633410 | Common:8; Rare:141; Clinvar:10; Clinvar (benign):4 | ||||
| chr5:7868997-7869218 | Common:2; Rare:114; Clinvar (benign):1 | ||||
| chr5:10353597-10353905 | Common:3; Rare:111 | ||||
| chr5:10354040-10354290 | Rare:88 | ||||
| chr5:10564167-10564340 | Common:1; Rare:58 | ||||
| chr5:10761064-10761490 | Common:14; Rare:141 |