| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:43125338-43125590 | Rare:54; Clinvar:3; Clinvar (benign):2 | ||||
| chr17:43171016-43171255 | Rare:79 | ||||
| chr17:43398872-43399000 | Common:1; Rare:38 | ||||
| chr17:43661306-43661508 | Common:1; Rare:83; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:44070612-44070918 | Common:3; Rare:103; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:44123594-44123840 | Common:3; Rare:72 | ||||
| chr17:44186691-44187038 | Rare:112 | ||||
| chr17:44187161-44187274 | Rare:31 | ||||
| chr17:44222103-44222269 | Rare:33 | ||||
| chr17:44324760-44324987 | Common:2; Rare:81 | ||||
| chr17:44345075-44345321 | Rare:51; Clinvar:5; Clinvar (benign):3 | ||||
| chr17:44350277-44350498 | Common:1; Rare:78; Clinvar:4; Clinvar (benign):3 | ||||
| chr17:44503371-44503727 | Rare:137 | ||||
| chr17:44656253-44656480 | Common:6; Rare:84 | ||||
| chr17:44899375-44899741 | Common:2; Rare:115; Clinvar:2; Clinvar (benign):1 |