| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:43171002-43171255 | Rare:84 | ||||
| chr17:43398923-43398996 | Rare:19 | ||||
| chr17:43778931-43779089 | Common:1; Rare:39 | ||||
| chr17:43833101-43833257 | Rare:42 | ||||
| chr17:44070581-44070941 | Common:3; Rare:117; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:44123585-44123844 | Common:3; Rare:74 | ||||
| chr17:44141780-44141956 | Common:1; Rare:36 | ||||
| chr17:44186658-44187002 | Common:1; Rare:127 | ||||
| chr17:44187178-44187250 | Rare:19 | ||||
| chr17:44220825-44221005 | Rare:54 | ||||
| chr17:44221200-44221373 | Rare:48 | ||||
| chr17:44221593-44221921 | Common:4; Rare:90 | ||||
| chr17:44308432-44308641 | Common:1; Rare:63 | ||||
| chr17:44324765-44324993 | Common:2; Rare:84 | ||||
| chr17:44345078-44345312 | Rare:50; Clinvar:5; Clinvar (benign):3 |