| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:111878909-111879016 | Common:1; Rare:52 | ||||
| chr11:111879154-111879582 | Common:1; Rare:134 | ||||
| chr11:111912712-111912868 | Rare:30 | ||||
| chr11:111913074-111913310 | Rare:48 | ||||
| chr11:111923722-111924082 | Common:2; Rare:61 | ||||
| chr11:111937125-111937429 | Common:7; Rare:90 | ||||
| chr11:111977135-111977388 | Common:3; Rare:57 | ||||
| chr11:112025328-112025646 | Common:2; Rare:105; Clinvar:1; Clinvar (benign):6 | ||||
| chr11:112073987-112074349 | Common:1; Rare:76 | ||||
| chr11:112086710-112086924 | Rare:92; Clinvar:4; Clinvar (pathogenic):3 | ||||
| chr11:112164083-112164133 | Rare:9 | ||||
| chr11:112226279-112226661 | Common:1; Rare:157; Clinvar:1; Clinvar (pathogenic):3 | ||||
| chr11:112961307-112961661 | Common:4; Rare:170 | ||||
| chr11:113314448-113314602 | Rare:54 | ||||
| chr11:113875472-113875797 | Common:4; Rare:121 |