| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:44564426-44565234 | Common:9; Rare:284 | ||||
| chr11:44565153-44565687 | Common:17; Rare:500 | ||||
| chr11:44950850-44951130 | Rare:69 | ||||
| chr11:45146424-45146861 | Common:13; Rare:275 | ||||
| chr11:45146891-45147520 | Common:7; Rare:656 | ||||
| chr11:45649470-45649860 | Common:5; Rare:177 | ||||
| chr11:45804147-45804547 | Common:2; Rare:117 | ||||
| chr11:45804874-45805274 | Common:20; Rare:442; Clinvar:30; Clinvar (benign):7 | ||||
| chr11:45805240-45805450 | Rare:40; Clinvar:4 | ||||
| chr11:45805363-45806050 | Common:4; Rare:183; Clinvar:9; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr11:45847153-45847557 | Common:8; Rare:587 | ||||
| chr11:45847907-45848307 | Common:1; Rare:88 | ||||
| chr11:45917620-45917983 | Rare:245; Clinvar:3 | ||||
| chr11:45917970-45918400 | Common:7; Rare:289; Clinvar:3; Clinvar (benign):4 | ||||
| chr11:45918674-45919074 | Common:3; Rare:204 |