| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:110507201-110507699 | Common:2; Rare:193 | ||||
| chr13:110561653-110561938 | Common:25; Rare:434 | ||||
| chr13:110615280-110615744 | Common:11; Rare:567 | ||||
| chr13:110615670-110615900 | Common:1; Rare:78 | ||||
| chr13:110705673-110706446 | Common:18; Rare:638; Clinvar:12; Clinvar (benign):34 | ||||
| chr13:110712297-110712813 | Common:3; Rare:495 | ||||
| chr13:110712820-110713527 | Common:19; Rare:1606 | ||||
| chr13:110713450-110713736 | Common:10; Rare:477 | ||||
| chr13:110714399-110714799 | Common:2; Rare:208 | ||||
| chr13:110714784-110715229 | Common:8; Rare:411 | ||||
| chr13:110715207-110715909 | Common:17; Rare:1510 | ||||
| chr13:110914266-110914851 | Common:30; Rare:838 | ||||
| chr13:110914932-110915685 | Common:77; Rare:1077 | ||||
| chr13:111153097-111153890 | Common:24; Rare:851 | ||||
| chr13:111154095-111154257 | Rare:68 |