| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44070612-44070958 | Common:3; Rare:121; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:44123591-44123840 | Common:3; Rare:72 | ||||
| chr17:44141626-44141941 | Common:2; Rare:60 | ||||
| chr17:44186666-44187002 | Common:1; Rare:121 | ||||
| chr17:44187178-44187264 | Rare:22 | ||||
| chr17:44210895-44211183 | Common:1; Rare:90 | ||||
| chr17:44221279-44221398 | Rare:35 | ||||
| chr17:44324744-44324936 | Common:2; Rare:73 | ||||
| chr17:44345025-44345334 | Rare:68; Clinvar:5; Clinvar (benign):4 | ||||
| chr17:44350506-44350744 | Rare:82; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:44352150-44352415 | Rare:86; Clinvar:9; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr17:44503366-44503720 | Rare:137 | ||||
| chr17:44708574-44708695 | Rare:25 | ||||
| chr17:44830756-44831028 | Rare:43 | ||||
| chr17:44899367-44899769 | Common:3; Rare:127; Clinvar:3; Clinvar (benign):1 |