| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:46225040-46225540 | Common:8; Rare:157 | ||||
| chr17:46922778-46923238 | Common:14; Rare:356; Clinvar:9; Clinvar (benign):27; Clinvar (pathogenic):1 | ||||
| chr17:47189100-47189660 | Common:2; Rare:205 | ||||
| chr17:47253580-47254110 | Common:8; Rare:136; Clinvar:1; Clinvar (benign):4 | ||||
| chr17:47323668-47324770 | Common:27; Rare:589 | ||||
| chr17:47530669-47531217 | Common:4; Rare:288 | ||||
| chr17:47649244-47650108 | Common:5; Rare:780 | ||||
| chr17:47650380-47650849 | Common:9; Rare:371 | ||||
| chr17:47693395-47693795 | Common:4; Rare:145 | ||||
| chr17:47693820-47694350 | Common:2; Rare:156 | ||||
| chr17:47694560-47694950 | Common:9; Rare:163 | ||||
| chr17:47821635-47821944 | Common:6; Rare:129 | ||||
| chr17:47831430-47831743 | Rare:281 | ||||
| chr17:47840400-47841560 | Common:1; Rare:428 | ||||
| chr17:47851106-47851469 | Common:9; Rare:179 |