| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:94768201-94768461 | Common:2; Rare:77 | ||||
| chr11:94973509-94973728 | Rare:71 | ||||
| chr11:95066826-95066935 | Rare:23 | ||||
| chr11:95067110-95067210 | Rare:31 | ||||
| chr11:95067429-95067573 | Rare:50 | ||||
| chr11:95089715-95089949 | Common:3; Rare:99 | ||||
| chr11:95789480-95789897 | Common:4; Rare:193 | ||||
| chr11:95790319-95790690 | Common:3; Rare:146 | ||||
| chr11:95923766-95924164 | Common:2; Rare:166; Clinvar:5; Clinvar (benign):5 | ||||
| chr11:96389820-96390059 | Common:1; Rare:100 | ||||
| chr11:100687723-100687772 | Rare:9 | ||||
| chr11:101914869-101915033 | Common:2; Rare:42 | ||||
| chr11:102110201-102110467 | Common:1; Rare:102 | ||||
| chr11:102317254-102317499 | Rare:48 | ||||
| chr11:102347063-102347444 | Common:8; Rare:106 |