| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:95790351-95790707 | Common:3; Rare:138 | ||||
| chr11:95923787-95924170 | Common:2; Rare:160; Clinvar:5; Clinvar (benign):5 | ||||
| chr11:96389846-96390050 | Common:1; Rare:87 | ||||
| chr11:99020593-99021062 | Rare:128 | ||||
| chr11:99021130-99021235 | Rare:19 | ||||
| chr11:101914862-101915059 | Common:3; Rare:57 | ||||
| chr11:101915106-101915369 | Common:3; Rare:78 | ||||
| chr11:102110223-102110454 | Rare:92 | ||||
| chr11:102317384-102317526 | Rare:39 | ||||
| chr11:102347131-102347354 | Common:2; Rare:80 | ||||
| chr11:102451846-102451995 | Rare:40 | ||||
| chr11:102452580-102452949 | Common:2; Rare:117 | ||||
| chr11:103092017-103092262 | Common:1; Rare:74 | ||||
| chr11:103109345-103109607 | Common:2; Rare:76; Clinvar:1; Clinvar (benign):3 | ||||
| chr11:105609918-105610395 | Common:2; Rare:95 |