| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:101914850-101915042 | Common:2; Rare:53 | ||||
| chr11:101915118-101915265 | Common:1; Rare:38 | ||||
| chr11:102047240-102047560 | Common:1; Rare:97 | ||||
| chr11:102110143-102110458 | Rare:112 | ||||
| chr11:102111337-102111885 | Common:1; Rare:157 | ||||
| chr11:102317151-102317651 | Common:2; Rare:126 | ||||
| chr11:102347002-102347307 | Common:7; Rare:90 | ||||
| chr11:102347499-102347899 | Common:3; Rare:153 | ||||
| chr11:102452712-102452978 | Common:1; Rare:82 | ||||
| chr11:102453010-102453320 | Rare:89 | ||||
| chr11:103092090-103092313 | Common:2; Rare:87 | ||||
| chr11:103109269-103109638 | Common:2; Rare:105; Clinvar:2; Clinvar (benign):3 | ||||
| chr11:104163512-104164588 | Common:16; Rare:521 | ||||
| chr11:106022183-106022601 | Common:3; Rare:121 | ||||
| chr11:106076934-106077046 | Rare:22 |