| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:14440923-14441141 | Common:3; Rare:71 | ||||
| chr5:16465442-16465895 | Rare:128 | ||||
| chr5:16616977-16617270 | Common:2; Rare:80; Clinvar (benign):5 | ||||
| chr5:16936235-16936498 | Common:3; Rare:80 | ||||
| chr5:31532037-31532395 | Common:4; Rare:103 | ||||
| chr5:31854168-31854591 | Common:4; Rare:89 | ||||
| chr5:31854747-31855132 | Common:2; Rare:130 | ||||
| chr5:31936069-31936169 | Rare:13 | ||||
| chr5:32077385-32077525 | Rare:45 | ||||
| chr5:32173946-32174120 | Rare:52 | ||||
| chr5:32174252-32174395 | Common:1; Rare:55 | ||||
| chr5:32255321-32255687 | Common:1; Rare:71 | ||||
| chr5:32444620-32444988 | Common:1; Rare:117 | ||||
| chr5:32586280-32586492 | Common:3; Rare:50 | ||||
| chr5:32712260-32712307 | Rare:12 |