| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:32031501-32031648 | Rare:28 | ||||
| chr13:32315339-32315563 | Common:1; Rare:62; Clinvar:2; Clinvar (benign):2 | ||||
| chr13:32315690-32316080 | Common:3; Rare:88; Clinvar (benign):4 | ||||
| chr13:32316098-32316498 | Common:1; Rare:117; Clinvar:7; Clinvar (benign):14; Clinvar (pathogenic):5 | ||||
| chr13:32538730-32538975 | Common:1; Rare:62 | ||||
| chr13:32586188-32586621 | Common:2; Rare:132 | ||||
| chr13:33285673-33285955 | Common:1; Rare:64 | ||||
| chr13:33817979-33818226 | Common:2; Rare:114 | ||||
| chr13:34941610-34942000 | Rare:72 | ||||
| chr13:34942151-34942361 | Common:3; Rare:66 | ||||
| chr13:36130570-36131010 | Common:3; Rare:107 | ||||
| chr13:36131280-36131561 | Rare:63 | ||||
| chr13:36297768-36297942 | Common:1; Rare:66 | ||||
| chr13:36346070-36346260 | Common:1; Rare:41; Clinvar (benign):1 | ||||
| chr13:36346634-36346912 | Common:4; Rare:79 |