| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44186614-44187006 | Common:1; Rare:139 | ||||
| chr17:44187161-44187274 | Rare:31 | ||||
| chr17:44220833-44221043 | Rare:64 | ||||
| chr17:44221200-44221345 | Rare:42 | ||||
| chr17:44222089-44222265 | Rare:36 | ||||
| chr17:44324744-44325025 | Common:3; Rare:101 | ||||
| chr17:44345064-44345324 | Rare:54; Clinvar:5; Clinvar (benign):3 | ||||
| chr17:44350506-44350780 | Rare:96; Clinvar:4; Clinvar (benign):3 | ||||
| chr17:44503363-44503760 | Rare:150 | ||||
| chr17:44708523-44708699 | Common:1; Rare:38 | ||||
| chr17:44708764-44708882 | Common:3; Rare:44 | ||||
| chr17:44898975-44899148 | Common:1; Rare:43 | ||||
| chr17:44899367-44899774 | Common:3; Rare:128; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:44947596-44947930 | Common:1; Rare:83 | ||||
| chr17:45051413-45051692 | Common:1; Rare:90 |