| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:34620451-34620607 | Common:1; Rare:42 | ||||
| chr9:34652015-34652205 | Rare:55 | ||||
| chr9:34665381-34665655 | Rare:89 | ||||
| chr9:35103073-35103157 | Common:1; Rare:46 | ||||
| chr9:35103160-35103292 | Rare:32 | ||||
| chr9:35161819-35162141 | Common:4; Rare:92 | ||||
| chr9:35563871-35563946 | Rare:25 | ||||
| chr9:35646823-35646978 | Common:1; Rare:34 | ||||
| chr9:35657686-35657816 | Common:2; Rare:83; Clinvar:11; Clinvar (benign):1; Clinvar (pathogenic):5 | ||||
| chr9:35657850-35658322 | Common:7; Rare:411; Clinvar:42; Clinvar (benign):15; Clinvar (pathogenic):40 | ||||
| chr9:35665193-35665334 | Common:2; Rare:49 | ||||
| chr9:35689702-35690120 | Common:4; Rare:129; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:35691059-35691212 | Common:1; Rare:30 | ||||
| chr9:35732076-35732334 | Common:2; Rare:70 | ||||
| chr9:35732364-35732669 | Common:2; Rare:77 |