| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:94768061-94768399 | Common:2; Rare:88 | ||||
| chr11:94973509-94973843 | Rare:94 | ||||
| chr11:95066704-95066939 | Rare:41 | ||||
| chr11:95067452-95067626 | Common:1; Rare:77 | ||||
| chr11:95231406-95231618 | Common:2; Rare:58 | ||||
| chr11:95789474-95789893 | Common:4; Rare:192 | ||||
| chr11:95790346-95790713 | Common:3; Rare:147 | ||||
| chr11:95923787-95924164 | Common:2; Rare:157; Clinvar:5; Clinvar (benign):5 | ||||
| chr11:96389854-96390073 | Common:2; Rare:91 | ||||
| chr11:99020835-99021184 | Rare:102 | ||||
| chr11:100687715-100687769 | Rare:9 | ||||
| chr11:101915121-101915363 | Common:3; Rare:71 | ||||
| chr11:102047334-102047480 | Common:1; Rare:48 | ||||
| chr11:102110302-102110464 | Rare:56 | ||||
| chr11:102112306-102112646 | Rare:74 |