| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:86800286-86800604 | Common:2; Rare:114 | ||||
| chr11:86954805-86955160 | Common:1; Rare:120; Clinvar:2; Clinvar (benign):4 | ||||
| chr11:86955344-86955664 | Common:1; Rare:107; Clinvar (benign):1 | ||||
| chr11:87037757-87038059 | Common:3; Rare:142 | ||||
| chr11:88175405-88175568 | Rare:71 | ||||
| chr11:88337510-88337892 | Common:4; Rare:167; Clinvar:7; Clinvar (benign):3 | ||||
| chr11:90222934-90223201 | Common:2; Rare:108 | ||||
| chr11:93197868-93198162 | Common:3; Rare:90 | ||||
| chr11:93537910-93538224 | Rare:77 | ||||
| chr11:93741381-93741702 | Common:7; Rare:131 | ||||
| chr11:93784189-93784374 | Common:3; Rare:55 | ||||
| chr11:93784533-93784585 | Rare:12 | ||||
| chr11:93784834-93784931 | Common:1; Rare:26 | ||||
| chr11:94128802-94129289 | Common:4; Rare:159 | ||||
| chr11:94493780-94494053 | Common:5; Rare:81; Clinvar:1; Clinvar (benign):2 |