| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:52129034-52129178 | Rare:36 | ||||
| chr13:52158903-52159248 | Common:5; Rare:71 | ||||
| chr13:52159386-52159423 | Rare:14 | ||||
| chr13:52159496-52159750 | Common:2; Rare:57 | ||||
| chr13:52159858-52159922 | Common:2; Rare:8 | ||||
| chr13:52449961-52450408 | Common:2; Rare:97 | ||||
| chr13:52450511-52450856 | Common:1; Rare:100 | ||||
| chr13:52455240-52455569 | Common:3; Rare:116 | ||||
| chr13:52455670-52455744 | Common:1; Rare:29 | ||||
| chr13:52455839-52456013 | Common:4; Rare:53 | ||||
| chr13:52652211-52652470 | Common:3; Rare:71 | ||||
| chr13:52652562-52652933 | Common:3; Rare:115 | ||||
| chr13:60163009-60163431 | Rare:56 | ||||
| chr13:60163662-60164193 | Common:4; Rare:156; Clinvar (benign):1 | ||||
| chr13:60396225-60396691 | Common:3; Rare:155 |