| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:43675400-43675860 | Common:11; Rare:75 | ||||
| chr17:43720710-43721170 | Common:5; Rare:96 | ||||
| chr17:43791630-43791960 | Common:1; Rare:39 | ||||
| chr17:43872403-43872597 | Common:1; Rare:52 | ||||
| chr17:43938026-43938426 | Common:5; Rare:155 | ||||
| chr17:44006604-44007389 | Common:11; Rare:331; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr17:44007302-44007702 | Common:1; Rare:201; Clinvar:7; Clinvar (benign):6; Clinvar (pathogenic):5 | ||||
| chr17:44087409-44087845 | Common:7; Rare:202 | ||||
| chr17:44095480-44095783 | Common:1; Rare:75 | ||||
| chr17:44095948-44096152 | Common:1; Rare:32 | ||||
| chr17:44138144-44138397 | Rare:51 | ||||
| chr17:44511859-44512107 | Rare:57 | ||||
| chr17:44539909-44540118 | Rare:41 | ||||
| chr17:44543562-44543843 | Common:1; Rare:55 | ||||
| chr17:44548003-44548242 | Common:1; Rare:37 |