| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65662779-65663410 | Common:17; Rare:565 | ||||
| chr11:65663337-65663737 | Common:3; Rare:123 | ||||
| chr11:65711032-65711654 | Common:3; Rare:161 | ||||
| chr11:65711747-65713051 | Common:14; Rare:1305 | ||||
| chr11:65720335-65721063 | Common:11; Rare:767; Clinvar:13; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr11:65780660-65781200 | Common:6; Rare:515 | ||||
| chr11:65856860-65857447 | Common:19; Rare:702 | ||||
| chr11:65857364-65858144 | Common:9; Rare:410 | ||||
| chr11:65858076-65858895 | Common:10; Rare:590 | ||||
| chr11:65859317-65859775 | Rare:586 | ||||
| chr11:65859686-65860343 | Common:2; Rare:254 | ||||
| chr11:65860266-65862017 | Common:37; Rare:2061 | ||||
| chr11:65867555-65867969 | Common:2; Rare:261; Clinvar:4; Clinvar (benign):4 | ||||
| chr11:65872984-65873857 | Common:16; Rare:617 | ||||
| chr11:65887783-65888183 | Common:4; Rare:147; Clinvar:1 |