| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18526390-18526730 | Common:6; Rare:118 | ||||
| chr11:18526808-18527049 | Common:2; Rare:194 | ||||
| chr11:18588633-18588996 | Common:4; Rare:183 | ||||
| chr11:18634332-18634596 | Common:2; Rare:88 | ||||
| chr11:18634720-18634950 | Common:3; Rare:69 | ||||
| chr11:19116957-19117259 | Common:6; Rare:153 | ||||
| chr11:19240625-19241620 | Common:2; Rare:397 | ||||
| chr11:19712598-19712865 | Common:4; Rare:179 | ||||
| chr11:20363646-20363811 | Common:7; Rare:65 | ||||
| chr11:20363915-20364212 | Common:12; Rare:95 | ||||
| chr11:20364450-20364680 | Rare:78 | ||||
| chr11:20387413-20387821 | Common:14; Rare:266 | ||||
| chr11:22625450-22625710 | Common:1; Rare:156; Clinvar:13; Clinvar (benign):5; Clinvar (pathogenic):3 | ||||
| chr11:22625797-22626021 | Common:5; Rare:123; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:22829210-22829470 | Common:3; Rare:102 |