| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:233488371-233488633 | Common:4; Rare:43 | ||||
| chr2:241545214-241545379 | Common:2; Rare:27 | ||||
| chr20:1418266-1418464 | Rare:28 | ||||
| chr20:4470365-4470506 | Common:1; Rare:17 | ||||
| chr20:9200721-9200992 | Rare:46 | ||||
| chr20:18524771-18524975 | Common:1; Rare:43 | ||||
| chr20:18793974-18794089 | Rare:36 | ||||
| chr20:36050613-36050783 | Common:1; Rare:58 | ||||
| chr20:36050896-36051150 | Common:3; Rare:91 | ||||
| chr20:45894708-45895009 | Common:3; Rare:108; Clinvar:2; Clinvar (benign):2 | ||||
| chr20:47357800-47357844 | Rare:9 | ||||
| chr20:50166052-50166344 | Common:1; Rare:76 | ||||
| chr20:62501897-62502063 | Common:1; Rare:32 | ||||
| chr21:10413191-10413538 | Common:1; Rare:39 | ||||
| chr21:18759814-18760105 | Common:3; Rare:93 |