| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:49936157-49936592 | Common:1; Rare:138 | ||||
| chr13:49996795-49997099 | Common:1; Rare:57 | ||||
| chr13:50081951-50082262 | Common:1; Rare:86 | ||||
| chr13:50909712-50910074 | Common:1; Rare:79; Clinvar:5; Clinvar (benign):1 | ||||
| chr13:51453013-51453388 | Rare:146 | ||||
| chr13:51804111-51804227 | Common:2; Rare:36 | ||||
| chr13:52012076-52012428 | Common:2; Rare:114; Clinvar:1 | ||||
| chr13:52455335-52455528 | Common:3; Rare:68 | ||||
| chr13:52652322-52652466 | Common:2; Rare:42 | ||||
| chr13:52652626-52652933 | Common:3; Rare:98 | ||||
| chr13:52653147-52653149 | |||||
| chr13:52848631-52848759 | Common:1; Rare:36 | ||||
| chr13:60163892-60164118 | Common:1; Rare:61 | ||||
| chr13:60397173-60397362 | Common:4; Rare:72 | ||||
| chr13:70108298-70108520 | Rare:43 |