| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:87037765-87038043 | Common:3; Rare:132 | ||||
| chr11:88337644-88337888 | Common:4; Rare:118; Clinvar:6; Clinvar (benign):3 | ||||
| chr11:90222989-90223153 | Common:1; Rare:63 | ||||
| chr11:93197893-93197969 | Rare:23 | ||||
| chr11:93741381-93741702 | Common:7; Rare:131 | ||||
| chr11:94493743-94494058 | Common:6; Rare:91; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:94973524-94973697 | Rare:58 | ||||
| chr11:95089747-95089939 | Common:3; Rare:80 | ||||
| chr11:95790365-95790685 | Common:3; Rare:119 | ||||
| chr11:95924071-95924119 | Rare:18 | ||||
| chr11:96389857-96390050 | Common:1; Rare:80 | ||||
| chr11:101914774-101915093 | Common:4; Rare:79 | ||||
| chr11:101915106-101915369 | Common:3; Rare:78 | ||||
| chr11:102110045-102110470 | Common:2; Rare:148 | ||||
| chr11:102317215-102317526 | Rare:58 |