| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:107457615-107458070 | Common:15; Rare:325 | ||||
| chr11:107564780-107565490 | Common:4; Rare:213 | ||||
| chr11:107565453-107565950 | Common:10; Rare:394 | ||||
| chr11:107565984-107566653 | Common:4; Rare:191 | ||||
| chr11:107858386-107859462 | Common:16; Rare:846 | ||||
| chr11:108008502-108009535 | Common:5; Rare:832 | ||||
| chr11:108009623-108009735 | Rare:32 | ||||
| chr11:108121279-108121679 | Common:25; Rare:483; Clinvar:7; Clinvar (benign):26; Clinvar (pathogenic):1 | ||||
| chr11:108121676-108122121 | Common:7; Rare:153 | ||||
| chr11:108221917-108222317 | Common:2; Rare:95 | ||||
| chr11:108222465-108223186 | Common:7; Rare:1297; Clinvar:52; Clinvar (benign):7 | ||||
| chr11:108223180-108223520 | Rare:132; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:108223451-108223890 | Common:6; Rare:291 | ||||
| chr11:108466892-108467292 | Common:3; Rare:134 | ||||
| chr11:108467335-108467905 | Common:25; Rare:747 |