| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:52455229-52455536 | Common:3; Rare:104 | ||||
| chr13:52652827-52652933 | Common:2; Rare:49 | ||||
| chr13:60163770-60164118 | Common:2; Rare:88 | ||||
| chr13:72727568-72727972 | Common:7; Rare:157 | ||||
| chr13:72781876-72782188 | Common:1; Rare:119 | ||||
| chr13:75635992-75636382 | Common:2; Rare:97 | ||||
| chr13:79406219-79406306 | Common:1; Rare:26 | ||||
| chr13:95676937-95677192 | Common:3; Rare:84 | ||||
| chr13:96053353-96053583 | Common:2; Rare:93 | ||||
| chr13:99200661-99200921 | Common:6; Rare:120 | ||||
| chr13:100088894-100089139 | Rare:90; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr13:102596788-102597035 | Common:1; Rare:118 | ||||
| chr13:102773699-102773860 | Rare:66 | ||||
| chr13:102798903-102799124 | Common:1; Rare:47 | ||||
| chr13:102845714-102846089 | Common:9; Rare:101; Clinvar:2; Clinvar (benign):4 |