| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7583473-7583942 | Common:1; Rare:179; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr17:7583979-7584192 | Rare:58 | ||||
| chr17:7614043-7614237 | Rare:60 | ||||
| chr17:7614533-7614689 | Rare:37 | ||||
| chr17:7614714-7614914 | Rare:53 | ||||
| chr17:7614984-7615452 | Rare:149 | ||||
| chr17:7627577-7627599 | Rare:5 | ||||
| chr17:7627711-7628016 | Common:3; Rare:103 | ||||
| chr17:7650689-7651004 | Common:2; Rare:92 | ||||
| chr17:7686005-7686563 | Rare:151 | ||||
| chr17:7686651-7686954 | Common:1; Rare:71 | ||||
| chr17:7687277-7687709 | Rare:83; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:7688076-7688596 | Common:5; Rare:119; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:7688730-7688774 | Rare:9 | ||||
| chr17:7704998-7705300 | Common:2; Rare:68 |