| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:47171734-47171910 | Common:2; Rare:33 | ||||
| chr11:47172375-47172518 | Rare:26 | ||||
| chr11:47176849-47177071 | Rare:92 | ||||
| chr11:47214264-47214485 | Common:1; Rare:28 | ||||
| chr11:47214814-47215097 | Common:2; Rare:67; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:47248765-47248944 | Rare:73 | ||||
| chr11:47269550-47269811 | Common:1; Rare:90 | ||||
| chr11:47269981-47270217 | Common:1; Rare:85 | ||||
| chr11:47408354-47408624 | Rare:89 | ||||
| chr11:47565493-47565635 | Common:3; Rare:27 | ||||
| chr11:47578952-47579106 | Rare:78; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47641826-47642128 | Rare:70 | ||||
| chr11:47642445-47642793 | Rare:128 | ||||
| chr11:47767170-47767428 | Common:2; Rare:116 | ||||
| chr11:47848325-47848406 | Rare:40 |