| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:43644113-43644280 | Common:1; Rare:33 | ||||
| chr11:43680515-43680811 | Common:1; Rare:90 | ||||
| chr11:43880654-43880887 | Common:2; Rare:57 | ||||
| chr11:43942385-43942639 | Common:3; Rare:60 | ||||
| chr11:44096060-44096390 | Common:2; Rare:86 | ||||
| chr11:44726833-44727012 | Common:8; Rare:35 | ||||
| chr11:44949691-44949996 | Common:2; Rare:64 | ||||
| chr11:44949998-44950883 | Common:9; Rare:312 | ||||
| chr11:45147141-45147350 | Common:1; Rare:82 | ||||
| chr11:45286183-45286583 | Rare:147 | ||||
| chr11:45804965-45805186 | Common:3; Rare:55; Clinvar:4; Clinvar (benign):1 | ||||
| chr11:45847233-45847517 | Common:2; Rare:120 | ||||
| chr11:45885370-45885770 | Common:2; Rare:109 | ||||
| chr11:45917812-45918274 | Common:1; Rare:120; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:45918778-45918908 | Rare:41 |