| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:93784196-93784391 | Common:3; Rare:57 | ||||
| chr11:94493773-94494021 | Common:4; Rare:73; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:94973537-94973711 | Rare:52 | ||||
| chr11:95789478-95789620 | Common:1; Rare:71 | ||||
| chr11:95789774-95790014 | Common:3; Rare:81 | ||||
| chr11:95790276-95790713 | Common:3; Rare:166 | ||||
| chr11:95923787-95924170 | Common:2; Rare:160; Clinvar:5; Clinvar (benign):5 | ||||
| chr11:96389820-96390043 | Common:1; Rare:90 | ||||
| chr11:102110168-102110467 | Common:1; Rare:111 | ||||
| chr11:102347111-102347291 | Common:2; Rare:58 | ||||
| chr11:102452659-102452943 | Common:1; Rare:90 | ||||
| chr11:103091931-103092278 | Common:2; Rare:101 | ||||
| chr11:103109294-103109577 | Common:1; Rare:82; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:106077287-106077740 | Common:2; Rare:148 | ||||
| chr11:107457734-107457965 | Common:3; Rare:78 |