| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:60906455-60906779 | Rare:81 | ||||
| chr11:61161402-61161732 | Common:1; Rare:93 | ||||
| chr11:61311789-61312024 | Rare:74 | ||||
| chr11:61333026-61333275 | Common:1; Rare:91 | ||||
| chr11:61361826-61361981 | Common:1; Rare:41 | ||||
| chr11:61362239-61362410 | Common:2; Rare:51; Clinvar:8; Clinvar (benign):1 | ||||
| chr11:61392527-61392649 | Common:2; Rare:41; Clinvar:3; Clinvar (benign):2 | ||||
| chr11:61429239-61429467 | Common:3; Rare:80 | ||||
| chr11:61429891-61430169 | Common:1; Rare:121; Clinvar:3; Clinvar (benign):5 | ||||
| chr11:61792564-61792942 | Common:5; Rare:103 | ||||
| chr11:61840440-61840696 | Common:1; Rare:53 | ||||
| chr11:61967285-61967709 | Common:3; Rare:159; Clinvar:4 | ||||
| chr11:62270109-62270258 | Common:1; Rare:40 | ||||
| chr11:62536467-62536767 | Rare:71 | ||||
| chr11:62545606-62545987 | Common:1; Rare:84 |