| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:36346301-36346454 | Common:2; Rare:41; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:36346632-36346818 | Common:4; Rare:55 | ||||
| chr13:37000468-37000805 | Common:3; Rare:106 | ||||
| chr13:37059600-37059754 | Common:1; Rare:51 | ||||
| chr13:37869759-37869920 | Common:1; Rare:36 | ||||
| chr13:38349548-38349917 | Common:3; Rare:126; Clinvar (pathogenic):1 | ||||
| chr13:38350208-38350474 | Common:1; Rare:82 | ||||
| chr13:38686920-38687133 | Common:2; Rare:57; Clinvar:3; Clinvar (benign):1 | ||||
| chr13:39038086-39038484 | Common:1; Rare:98 | ||||
| chr13:39603099-39603443 | Common:2; Rare:123 | ||||
| chr13:39655628-39655763 | Common:2; Rare:75; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr13:40771130-40771358 | Common:3; Rare:75 | ||||
| chr13:40789368-40789609 | Common:2; Rare:79; Clinvar:5; Clinvar (benign):2 | ||||
| chr13:41060889-41061645 | Common:20; Rare:294 | ||||
| chr13:41132732-41132984 | Rare:70 |