| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:44565318-44565717 | Common:8; Rare:265 | ||||
| chr11:44949446-44949977 | Common:13; Rare:185 | ||||
| chr11:44950635-44950955 | Common:4; Rare:116 | ||||
| chr11:45146522-45146811 | Common:4; Rare:112 | ||||
| chr11:45147017-45147450 | Common:5; Rare:393 | ||||
| chr11:45665520-45665940 | Common:4; Rare:162 | ||||
| chr11:45804024-45804603 | Common:4; Rare:229 | ||||
| chr11:45804859-45805305 | Common:9; Rare:260; Clinvar:15; Clinvar (benign):3 | ||||
| chr11:45805208-45805844 | Common:5; Rare:191; Clinvar:14; Clinvar (benign):5 | ||||
| chr11:45847125-45847685 | Common:6; Rare:499 | ||||
| chr11:45917763-45918162 | Common:2; Rare:253; Clinvar:8; Clinvar (benign):2 | ||||
| chr11:45918733-45918861 | Common:1; Rare:35 | ||||
| chr11:45922270-45922910 | Common:18; Rare:320 | ||||
| chr11:46119248-46120282 | Common:19; Rare:388 | ||||
| chr11:46120530-46121360 | Common:6; Rare:257 |