| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:6481302-6481524 | Common:4; Rare:88 | ||||
| chr11:6603553-6603860 | Common:4; Rare:91; Clinvar (benign):3 | ||||
| chr11:6619377-6619612 | Common:3; Rare:72; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr11:6656298-6656554 | Rare:39 | ||||
| chr11:6683267-6683426 | Common:3; Rare:78 | ||||
| chr11:7020308-7020510 | Rare:70 | ||||
| chr11:7513626-7513983 | Common:6; Rare:108 | ||||
| chr11:8168985-8169089 | Common:2; Rare:35 | ||||
| chr11:8682638-8682816 | Common:2; Rare:79 | ||||
| chr11:8718026-8718184 | Common:6; Rare:34 | ||||
| chr11:8910928-8911261 | Common:6; Rare:93 | ||||
| chr11:8964348-8964570 | Common:4; Rare:84 | ||||
| chr11:8964932-8965002 | Common:1; Rare:16 | ||||
| chr11:9265386-9265494 | Common:1; Rare:38 | ||||
| chr11:9314519-9314903 | Common:5; Rare:118 |