| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:49443981-49444448 | Common:1; Rare:146 | ||||
| chr13:49585465-49585628 | Common:1; Rare:52 | ||||
| chr13:49691255-49691413 | Rare:53 | ||||
| chr13:49691438-49691603 | Common:2; Rare:61 | ||||
| chr13:49936224-49936575 | Common:1; Rare:107 | ||||
| chr13:50081960-50082308 | Common:1; Rare:98 | ||||
| chr13:50909715-50910435 | Common:3; Rare:178; Clinvar:6; Clinvar (benign):1 | ||||
| chr13:51453011-51453416 | Common:1; Rare:156 | ||||
| chr13:51804103-51804227 | Common:2; Rare:39 | ||||
| chr13:52012079-52012457 | Common:2; Rare:139; Clinvar:1 | ||||
| chr13:52450044-52450175 | Rare:27 | ||||
| chr13:52450550-52450720 | Common:1; Rare:49 | ||||
| chr13:52455274-52455622 | Common:3; Rare:125 | ||||
| chr13:52455922-52456029 | Common:1; Rare:35 | ||||
| chr13:52652655-52652957 | Common:3; Rare:101 |