| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:106077263-106077713 | Common:2; Rare:136 | ||||
| chr11:107017748-107018054 | Common:2; Rare:109 | ||||
| chr11:107018396-107018700 | Common:4; Rare:85 | ||||
| chr11:107457751-107458007 | Common:5; Rare:88 | ||||
| chr11:107565490-107565842 | Common:2; Rare:93 | ||||
| chr11:107928089-107928564 | Common:5; Rare:114 | ||||
| chr11:107928878-107929034 | Rare:33 | ||||
| chr11:108008786-108008968 | Rare:52 | ||||
| chr11:108009283-108009389 | Rare:48 | ||||
| chr11:108121352-108121607 | Common:4; Rare:83; Clinvar:1; Clinvar (benign):4 | ||||
| chr11:108222551-108222800 | Rare:93 | ||||
| chr11:108223408-108224039 | Common:4; Rare:183 | ||||
| chr11:108467315-108467698 | Common:4; Rare:127 | ||||
| chr11:108552106-108552506 | Common:14; Rare:130 | ||||
| chr11:108593760-108593978 | Common:4; Rare:49 |