| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:45804974-45805186 | Common:3; Rare:53; Clinvar:4; Clinvar (benign):1 | ||||
| chr11:45847245-45847488 | Common:2; Rare:97 | ||||
| chr11:45917818-45918180 | Common:1; Rare:93; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:46119397-46119594 | Common:1; Rare:42 | ||||
| chr11:46119794-46120139 | Common:3; Rare:77 | ||||
| chr11:46120941-46121262 | Common:2; Rare:48 | ||||
| chr11:46361492-46361613 | Rare:28 | ||||
| chr11:46371306-46371555 | Rare:69 | ||||
| chr11:46380733-46380902 | Rare:48 | ||||
| chr11:46617239-46617600 | Common:5; Rare:101 | ||||
| chr11:46700549-46701077 | Common:4; Rare:133 | ||||
| chr11:46846224-46846421 | Common:1; Rare:56 | ||||
| chr11:47168308-47168624 | Common:1; Rare:60 | ||||
| chr11:47176837-47177161 | Common:1; Rare:135 | ||||
| chr11:47214366-47214457 | Rare:8 |