| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:47208680-47209550 | Common:1; Rare:554; Clinvar:2 | ||||
| chr17:47209598-47209770 | Common:1; Rare:85 | ||||
| chr17:47209812-47210514 | Common:8; Rare:153 | ||||
| chr17:47253580-47254028 | Common:16; Rare:400; Clinvar:5; Clinvar (benign):18 | ||||
| chr17:47254010-47254190 | Common:4; Rare:45 | ||||
| chr17:47291478-47292066 | Common:6; Rare:277 | ||||
| chr17:47323426-47324080 | Common:20; Rare:614 | ||||
| chr17:47324155-47324580 | Common:9; Rare:185 | ||||
| chr17:47530849-47531256 | Common:6; Rare:401 | ||||
| chr17:47648914-47649468 | Common:1; Rare:291 | ||||
| chr17:47649399-47650103 | Common:11; Rare:1467 | ||||
| chr17:47650260-47650419 | Rare:65 | ||||
| chr17:47650403-47650854 | Common:22; Rare:862 | ||||
| chr17:47656492-47657095 | Common:4; Rare:212 | ||||
| chr17:47693500-47693870 | Common:2; Rare:68 |