| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:4949857-4950145 | Common:1; Rare:64 | ||||
| chr17:4951016-4951155 | Common:1; Rare:32; Clinvar (benign):1 | ||||
| chr17:4966920-4967632 | Common:5; Rare:191 | ||||
| chr17:4967781-4967983 | Rare:76 | ||||
| chr17:4987387-4987787 | Common:3; Rare:123 | ||||
| chr17:5078141-5078542 | Common:4; Rare:99 | ||||
| chr17:5191826-5192132 | Common:2; Rare:99 | ||||
| chr17:5419604-5420006 | Common:6; Rare:118 | ||||
| chr17:5420103-5420272 | Rare:72 | ||||
| chr17:5438840-5439002 | Rare:52 | ||||
| chr17:5439120-5439253 | Common:3; Rare:36 | ||||
| chr17:5468762-5469142 | Common:3; Rare:142 | ||||
| chr17:5486157-5486639 | Common:5; Rare:160 | ||||
| chr17:5486796-5486949 | Common:4; Rare:45 | ||||
| chr17:5501001-5501270 | Common:3; Rare:81 |