| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67428324-67428531 | Rare:72 | ||||
| chr11:67482906-67483154 | Rare:55; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:68030360-68030746 | Common:3; Rare:109; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68038915-68039064 | Rare:44; Clinvar:1 | ||||
| chr11:68271891-68272146 | Common:2; Rare:110 | ||||
| chr11:68903770-68903943 | Common:4; Rare:81; Clinvar (benign):6 | ||||
| chr11:69299121-69299207 | Common:1; Rare:16 | ||||
| chr11:69640985-69641234 | Common:1; Rare:52 | ||||
| chr11:69675309-69675503 | Rare:53 | ||||
| chr11:70398439-70398596 | Common:2; Rare:53 | ||||
| chr11:71448334-71448697 | Common:4; Rare:97; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:71787350-71787546 | Common:12; Rare:82 | ||||
| chr11:71928915-71929058 | Common:1; Rare:47 | ||||
| chr11:72080449-72080853 | Common:2; Rare:90; Clinvar:7 | ||||
| chr11:72112653-72112854 | Common:2; Rare:89 |