| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:51862077-51862215 | Rare:20 | ||||
| chr13:51978963-51979081 | Common:2; Rare:25 | ||||
| chr13:52011982-52012428 | Common:2; Rare:144; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr13:52128773-52129160 | Common:2; Rare:101 | ||||
| chr13:52159221-52159514 | Common:5; Rare:77 | ||||
| chr13:52159553-52159654 | Common:1; Rare:21 | ||||
| chr13:52450197-52450454 | Common:2; Rare:51 | ||||
| chr13:52450592-52450694 | Rare:33 | ||||
| chr13:52455279-52455543 | Common:3; Rare:94 | ||||
| chr13:52455653-52456009 | Common:6; Rare:112 | ||||
| chr13:52652322-52652953 | Common:5; Rare:188 | ||||
| chr13:60012660-60012730 | Rare:17 | ||||
| chr13:60013156-60013264 | Common:1; Rare:24 | ||||
| chr13:60163892-60164118 | Common:1; Rare:61 | ||||
| chr13:60396291-60396538 | Common:2; Rare:94 |