| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:1799771-1799977 | Common:8; Rare:99 | ||||
| chr5:1801283-1801525 | Common:4; Rare:127; Clinvar:3; Clinvar (benign):3 | ||||
| chr5:5422388-5422717 | Common:2; Rare:111 | ||||
| chr5:6632970-6633530 | Common:8; Rare:166; Clinvar:10; Clinvar (benign):4 | ||||
| chr5:7868981-7869209 | Common:2; Rare:118; Clinvar (benign):1 | ||||
| chr5:9546073-9546307 | Common:6; Rare:53 | ||||
| chr5:10249866-10250353 | Common:19; Rare:234; Clinvar:4; Clinvar (benign):2 | ||||
| chr5:16465152-16465435 | Rare:89 | ||||
| chr5:31532040-31532455 | Common:5; Rare:121 | ||||
| chr5:32174244-32174398 | Common:1; Rare:58 | ||||
| chr5:33440643-33441095 | Common:7; Rare:127 | ||||
| chr5:34656159-34656459 | Common:3; Rare:75 | ||||
| chr5:34915491-34915870 | Common:2; Rare:113 | ||||
| chr5:36151897-36152173 | Rare:84 | ||||
| chr5:36876642-36876905 | Common:1; Rare:79; Clinvar:1; Clinvar (benign):1 |