| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66370762-66371447 | Common:2; Rare:280 | ||||
| chr11:66371610-66372290 | Common:16; Rare:744 | ||||
| chr11:66372340-66372650 | Common:3; Rare:138 | ||||
| chr11:66438043-66439300 | Common:14; Rare:912 | ||||
| chr11:66466064-66466464 | Rare:80 | ||||
| chr11:66466600-66467084 | Common:1; Rare:727 | ||||
| chr11:66479322-66479806 | Common:7; Rare:145 | ||||
| chr11:66480129-66480891 | Common:22; Rare:660 | ||||
| chr11:66510401-66510801 | Common:9; Rare:393; Clinvar:7; Clinvar (benign):4; Clinvar (pathogenic):12 | ||||
| chr11:66510824-66511224 | Common:3; Rare:127; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr11:66545966-66546366 | Common:17; Rare:341 | ||||
| chr11:66568422-66568822 | Common:10; Rare:228; Clinvar:1 | ||||
| chr11:66592592-66593335 | Common:8; Rare:733 | ||||
| chr11:66616164-66616733 | Common:8; Rare:719 | ||||
| chr11:66616681-66617178 | Common:2; Rare:350 |