| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:69675300-69675478 | Rare:51 | ||||
| chr11:70203144-70203345 | Common:3; Rare:76 | ||||
| chr11:70270463-70270805 | Common:2; Rare:136 | ||||
| chr11:70398410-70398621 | Common:2; Rare:79 | ||||
| chr11:71448347-71448711 | Common:4; Rare:96; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:71787312-71787546 | Common:14; Rare:91 | ||||
| chr11:71928659-71929085 | Common:1; Rare:117 | ||||
| chr11:72009131-72009348 | Rare:80 | ||||
| chr11:72009360-72009546 | Common:1; Rare:47 | ||||
| chr11:72041056-72041167 | Common:1; Rare:18 | ||||
| chr11:72041519-72041769 | Rare:43 | ||||
| chr11:72041846-72041911 | Common:2; Rare:11 | ||||
| chr11:72041921-72042088 | Rare:35 | ||||
| chr11:72080232-72080341 | Common:6; Rare:15 | ||||
| chr11:72080368-72080853 | Common:2; Rare:116; Clinvar:9 |