| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:78417777-78418023 | Common:1; Rare:97 | ||||
| chr11:78574773-78574940 | Common:2; Rare:66; Clinvar (benign):1 | ||||
| chr11:82900405-82900574 | Rare:46 | ||||
| chr11:83071784-83072111 | Common:4; Rare:93 | ||||
| chr11:83193629-83193786 | Common:1; Rare:71 | ||||
| chr11:83285908-83286130 | Common:3; Rare:104 | ||||
| chr11:83286312-83286475 | Rare:42 | ||||
| chr11:85627770-85628040 | Common:1; Rare:54 | ||||
| chr11:85628338-85628632 | Common:6; Rare:98 | ||||
| chr11:85682852-85683132 | Common:2; Rare:92 | ||||
| chr11:85686140-85686349 | Common:2; Rare:46 | ||||
| chr11:87037765-87038069 | Common:3; Rare:141 | ||||
| chr11:88337542-88337892 | Common:4; Rare:157; Clinvar:7; Clinvar (benign):3 | ||||
| chr11:90223015-90223141 | Common:1; Rare:49 | ||||
| chr11:93741403-93741695 | Common:7; Rare:121 |