| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:8232424-8232569 | Rare:33; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr17:8234909-8235111 | Common:1; Rare:57; Clinvar (benign):1 | ||||
| chr17:8248029-8248134 | Common:2; Rare:53; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:8249024-8249319 | Common:1; Rare:64 | ||||
| chr17:8295323-8295532 | Common:1; Rare:54 | ||||
| chr17:8435706-8436042 | Common:4; Rare:127 | ||||
| chr17:8867639-8867816 | Common:1; Rare:33 | ||||
| chr17:8965667-8965789 | Common:1; Rare:36 | ||||
| chr17:10114542-10114814 | Common:2; Rare:47 | ||||
| chr17:10657305-10657545 | Common:4; Rare:69 | ||||
| chr17:10697381-10697654 | Common:3; Rare:121; Clinvar:5; Clinvar (benign):6 | ||||
| chr17:10729725-10729841 | Rare:59 | ||||
| chr17:10729974-10730119 | Common:3; Rare:33 | ||||
| chr17:10838057-10838243 | Rare:23 | ||||
| chr17:11997444-11997618 | Common:3; Rare:60 |