| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:21603524-21603649 | Rare:32 | ||||
| chr13:21603651-21603990 | Rare:144 | ||||
| chr13:21604033-21604380 | Common:6; Rare:155 | ||||
| chr13:21670897-21671168 | Common:1; Rare:90; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:23374945-23375286 | Common:3; Rare:94; Clinvar:5; Clinvar (benign):2 | ||||
| chr13:23375294-23375573 | Common:2; Rare:113 | ||||
| chr13:23375577-23375832 | Common:3; Rare:68 | ||||
| chr13:23578775-23578946 | Common:1; Rare:44 | ||||
| chr13:23579181-23579388 | Common:5; Rare:73 | ||||
| chr13:23888492-23888994 | Common:2; Rare:112 | ||||
| chr13:23889123-23889189 | Rare:16 | ||||
| chr13:23889230-23889567 | Common:1; Rare:117 | ||||
| chr13:23979690-23979724 | Common:1; Rare:7 | ||||
| chr13:23980239-23980440 | Common:1; Rare:60 | ||||
| chr13:24160541-24160965 | Common:2; Rare:109 |