| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:52455335-52455543 | Common:3; Rare:78 | ||||
| chr13:52652679-52652926 | Common:3; Rare:86 | ||||
| chr13:52653066-52653164 | Rare:34 | ||||
| chr13:60163772-60164118 | Common:2; Rare:88 | ||||
| chr13:60397173-60397349 | Common:4; Rare:66 | ||||
| chr13:72727568-72727978 | Common:7; Rare:161 | ||||
| chr13:72781876-72782198 | Common:1; Rare:124 | ||||
| chr13:75549470-75549847 | Common:8; Rare:96 | ||||
| chr13:75635986-75636347 | Common:2; Rare:91 | ||||
| chr13:77027142-77027406 | Common:6; Rare:83 | ||||
| chr13:77918800-77918946 | Common:1; Rare:33 | ||||
| chr13:79405795-79405898 | Rare:34 | ||||
| chr13:79406219-79406314 | Common:1; Rare:29 | ||||
| chr13:79481041-79481467 | Common:2; Rare:171 | ||||
| chr13:93226684-93226957 | Common:2; Rare:50; Clinvar (benign):1 |