| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:119094259-119094600 | Common:1; Rare:68 | ||||
| chr11:119144961-119145121 | Rare:30 | ||||
| chr11:119339641-119339858 | Rare:73; Clinvar:3; Clinvar (benign):2 | ||||
| chr11:119361127-119361255 | Rare:30 | ||||
| chr11:119361306-119361485 | Rare:27 | ||||
| chr11:119361505-119361698 | Common:1; Rare:41 | ||||
| chr11:119368407-119368728 | Common:1; Rare:70 | ||||
| chr11:119584282-119584501 | Common:2; Rare:61 | ||||
| chr11:119584809-119584897 | Rare:11 | ||||
| chr11:119626351-119626609 | Common:3; Rare:46 | ||||
| chr11:119661843-119661986 | Common:2; Rare:33 | ||||
| chr11:119713344-119713638 | Common:3; Rare:50 | ||||
| chr11:119832668-119832836 | Common:2; Rare:26 | ||||
| chr11:119864477-119864568 | Common:1; Rare:21 | ||||
| chr11:119907132-119907499 | Common:1; Rare:68 |