| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:52455928-52456040 | Common:1; Rare:38 | ||||
| chr13:52652424-52652955 | Common:3; Rare:159 | ||||
| chr13:52653022-52653188 | Common:1; Rare:58 | ||||
| chr13:60163595-60164118 | Common:5; Rare:158; Clinvar (benign):2 | ||||
| chr13:67230263-67230666 | Common:2; Rare:127 | ||||
| chr13:72727529-72727975 | Common:7; Rare:178 | ||||
| chr13:72781283-72781611 | Common:1; Rare:83 | ||||
| chr13:72781626-72782216 | Common:2; Rare:218 | ||||
| chr13:75549378-75549881 | Common:9; Rare:142 | ||||
| chr13:75635573-75635942 | Common:4; Rare:107 | ||||
| chr13:75636407-75636727 | Common:1; Rare:84 | ||||
| chr13:75834719-75834988 | Common:1; Rare:45 | ||||
| chr13:76991741-76992199 | Common:5; Rare:158; Clinvar:21; Clinvar (benign):17; Clinvar (pathogenic):3 | ||||
| chr13:77027122-77027298 | Common:5; Rare:58 | ||||
| chr13:78659111-78659249 | Common:2; Rare:96 |