| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:1799785-1799977 | Common:7; Rare:93 | ||||
| chr5:1801300-1801468 | Common:4; Rare:85; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:7868991-7869204 | Common:2; Rare:109; Clinvar (benign):1 | ||||
| chr5:9545976-9546299 | Common:9; Rare:80 | ||||
| chr5:10249874-10250160 | Common:16; Rare:138 | ||||
| chr5:10353597-10353901 | Common:3; Rare:111 | ||||
| chr5:16465723-16465855 | Rare:22 | ||||
| chr5:31532052-31532356 | Common:3; Rare:87 | ||||
| chr5:32174252-32174398 | Common:1; Rare:55 | ||||
| chr5:33440606-33441109 | Common:7; Rare:140 | ||||
| chr5:34656158-34656473 | Common:3; Rare:80 | ||||
| chr5:34915472-34915750 | Common:1; Rare:70 | ||||
| chr5:36151876-36152174 | Rare:92 | ||||
| chr5:36606456-36606626 | Rare:32 | ||||
| chr5:36876657-36876889 | Common:1; Rare:70; Clinvar:1; Clinvar (benign):1 |