| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44210425-44210682 | Rare:99 | ||||
| chr17:44220841-44221163 | Common:1; Rare:113 | ||||
| chr17:44221257-44221309 | Rare:17 | ||||
| chr17:44221313-44221378 | Rare:17 | ||||
| chr17:44222089-44222378 | Rare:60 | ||||
| chr17:44324780-44324976 | Common:2; Rare:71 | ||||
| chr17:44345057-44345321 | Rare:55; Clinvar:5; Clinvar (benign):3 | ||||
| chr17:44503377-44503717 | Rare:133 | ||||
| chr17:44708508-44708699 | Common:1; Rare:41 | ||||
| chr17:44899369-44899476 | Rare:44 | ||||
| chr17:44947588-44947903 | Common:1; Rare:75 | ||||
| chr17:45060987-45061332 | Common:2; Rare:91 | ||||
| chr17:45148170-45148476 | Common:1; Rare:91 | ||||
| chr17:45317008-45317343 | Common:4; Rare:82 | ||||
| chr17:45410376-45410458 | Rare:12 |