| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:9459844-9460027 | Rare:49 | ||||
| chr11:9460309-9460361 | Common:1; Rare:8 | ||||
| chr11:9460528-9461521 | Common:10; Rare:299 | ||||
| chr11:9572976-9573456 | Common:7; Rare:125 | ||||
| chr11:9573462-9573827 | Rare:107 | ||||
| chr11:9573847-9573953 | Rare:25 | ||||
| chr11:9573991-9574054 | Rare:16 | ||||
| chr11:9575086-9575253 | Rare:44 | ||||
| chr11:9575422-9575545 | Common:2; Rare:16 | ||||
| chr11:9663847-9664191 | Common:4; Rare:113 | ||||
| chr11:9664312-9664522 | Rare:46 | ||||
| chr11:10293835-10294084 | Common:3; Rare:56; Clinvar (pathogenic):1 | ||||
| chr11:10294114-10294348 | Common:2; Rare:83; Clinvar:4 | ||||
| chr11:10294542-10294744 | Rare:45 | ||||
| chr11:10304196-10304289 | Rare:16 |