| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:62663118-62663205 | Rare:16 | ||||
| chr20:62773015-62773382 | Common:3; Rare:75 | ||||
| chr21:43755716-43755967 | Common:1; Rare:86 | ||||
| chr21:43977348-43977542 | Common:3; Rare:52 | ||||
| chr22:20702631-20702963 | Common:3; Rare:76 | ||||
| chr22:26482102-26482340 | Common:1; Rare:37; Clinvar:1 | ||||
| chr22:30578858-30579188 | Common:2; Rare:96 | ||||
| chr22:30969044-30969223 | Common:2; Rare:55 | ||||
| chr22:37805901-37806403 | Common:3; Rare:137 | ||||
| chr22:37972089-37972364 | Common:1; Rare:57; Clinvar:1 | ||||
| chr22:41697250-41697428 | Rare:41 | ||||
| chr22:50526958-50527214 | Common:1; Rare:88; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14744714-14744895 | Common:1; Rare:28 | ||||
| chr3:14943278-14943530 | Common:1; Rare:72 | ||||
| chr3:49357221-49357260 | Rare:10 |