| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:95923776-95924172 | Common:2; Rare:162; Clinvar:5; Clinvar (benign):5 | ||||
| chr11:96389857-96390071 | Common:2; Rare:88 | ||||
| chr11:101914874-101915033 | Common:2; Rare:40 | ||||
| chr11:101915106-101915310 | Common:3; Rare:58 | ||||
| chr11:102110089-102110454 | Common:1; Rare:131 | ||||
| chr11:102111989-102112264 | Common:1; Rare:75 | ||||
| chr11:102317234-102317499 | Rare:48 | ||||
| chr11:102347144-102347376 | Common:2; Rare:85 | ||||
| chr11:102452612-102452946 | Common:2; Rare:103 | ||||
| chr11:103092028-103092262 | Common:1; Rare:72 | ||||
| chr11:106077306-106077700 | Common:2; Rare:116 | ||||
| chr11:107565704-107565780 | Rare:22 | ||||
| chr11:108009307-108009357 | Rare:24 | ||||
| chr11:108121404-108121608 | Common:4; Rare:70; Clinvar:1; Clinvar (benign):4 | ||||
| chr11:108222585-108222983 | Rare:129; Clinvar:3 |