| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:8964361-8964531 | Common:4; Rare:60 | ||||
| chr11:8964920-8965025 | Common:1; Rare:27 | ||||
| chr11:9003986-9004121 | Rare:53 | ||||
| chr11:9314519-9314953 | Common:6; Rare:126 | ||||
| chr11:9384561-9384776 | Common:1; Rare:82 | ||||
| chr11:9460609-9461035 | Common:4; Rare:111 | ||||
| chr11:9663993-9664180 | Common:4; Rare:69 | ||||
| chr11:10455125-10455432 | Common:5; Rare:55; Clinvar:2; Clinvar (benign):6 | ||||
| chr11:10541145-10541262 | Rare:43 | ||||
| chr11:10750695-10751038 | Common:4; Rare:92 | ||||
| chr11:10751159-10751306 | Rare:44 | ||||
| chr11:10808744-10808775 | Rare:8 | ||||
| chr11:10808888-10809117 | Rare:98 | ||||
| chr11:10858013-10858282 | Common:3; Rare:87 | ||||
| chr11:11621967-11622198 | Common:3; Rare:89 |