| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:43590872-43591039 | Rare:49 | ||||
| chr20:43666770-43667090 | Common:5; Rare:103 | ||||
| chr20:43914609-43914951 | Common:4; Rare:90 | ||||
| chr20:44210590-44211112 | Common:5; Rare:182 | ||||
| chr20:44521853-44522243 | Common:3; Rare:123 | ||||
| chr20:44531773-44532187 | Common:3; Rare:120 | ||||
| chr20:44651611-44651822 | Common:1; Rare:67; Clinvar (benign):1 | ||||
| chr20:44885658-44885883 | Common:4; Rare:80 | ||||
| chr20:44966354-44966587 | Common:2; Rare:92 | ||||
| chr20:45362948-45363216 | Rare:85 | ||||
| chr20:45363366-45363656 | Common:3; Rare:83 | ||||
| chr20:45406150-45406207 | Rare:11 | ||||
| chr20:45406541-45406723 | Rare:46 | ||||
| chr20:45416229-45416693 | Rare:141; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr20:45791912-45792094 | Common:3; Rare:67 |