| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:31509472-31509957 | Common:12; Rare:955 | ||||
| chr11:31509990-31510150 | Common:2; Rare:109 | ||||
| chr11:31810397-31810797 | Common:4; Rare:117 | ||||
| chr11:31811040-31811530 | Rare:428; Clinvar:17 | ||||
| chr11:31812130-31812390 | Common:10; Rare:84 | ||||
| chr11:31815951-31816451 | Common:6; Rare:350 | ||||
| chr11:32090810-32091210 | Common:9; Rare:329 | ||||
| chr11:32091528-32091950 | Common:4; Rare:216 | ||||
| chr11:32434434-32435810 | Common:18; Rare:1212; Clinvar:144; Clinvar (benign):70; Clinvar (pathogenic):2 | ||||
| chr11:32435758-32436158 | Common:6; Rare:183 | ||||
| chr11:32583062-32583511 | Common:9; Rare:161 | ||||
| chr11:32583513-32584266 | Common:2; Rare:692 | ||||
| chr11:32584536-32584936 | Common:3; Rare:70 | ||||
| chr11:32892408-32893237 | Common:17; Rare:941 | ||||
| chr11:32893260-32894059 | Rare:503 |