| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44326765-44327010 | Common:1; Rare:83 | ||||
| chr17:44348655-44349728 | Common:3; Rare:316; Clinvar:13; Clinvar (benign):7; Clinvar (pathogenic):5 | ||||
| chr17:44511764-44512164 | Common:1; Rare:190 | ||||
| chr17:44587273-44587673 | Common:2; Rare:153 | ||||
| chr17:44797710-44798250 | Common:1; Rare:115 | ||||
| chr17:45043230-45043824 | Common:9; Rare:225 | ||||
| chr17:45050380-45050808 | Common:4; Rare:122 | ||||
| chr17:45102110-45102420 | Common:4; Rare:82 | ||||
| chr17:45149268-45149520 | Rare:146 | ||||
| chr17:45149752-45150037 | Common:2; Rare:88 | ||||
| chr17:45150160-45150450 | Common:2; Rare:116 | ||||
| chr17:45170792-45171362 | Common:4; Rare:137 | ||||
| chr17:45171380-45172010 | Common:1; Rare:214 | ||||
| chr17:45172880-45173310 | Common:3; Rare:104 | ||||
| chr17:45176161-45176776 | Common:7; Rare:260 |