| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:64777677-64778030 | Common:1; Rare:151 | ||||
| chr11:64778413-64778842 | Common:3; Rare:190 | ||||
| chr11:64778916-64779457 | Common:10; Rare:128 | ||||
| chr11:64803152-64803443 | Rare:108 | ||||
| chr11:64803642-64803778 | Rare:42 | ||||
| chr11:64809810-64810038 | Rare:49; Clinvar:12; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr11:64810501-64810747 | Common:2; Rare:57; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:64844588-64844908 | Common:4; Rare:91 | ||||
| chr11:64856324-64856553 | Common:1; Rare:39 | ||||
| chr11:64856598-64856892 | Common:1; Rare:58 | ||||
| chr11:64877965-64878180 | Rare:64 | ||||
| chr11:64878437-64878983 | Common:4; Rare:190 | ||||
| chr11:64878989-64879164 | Rare:28 | ||||
| chr11:64879251-64879300 | Rare:8 | ||||
| chr11:64888004-64888089 | Common:1; Rare:30 |