| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:34961479-34961569 | Common:1; Rare:41 | ||||
| chr17:35242920-35243076 | Rare:51 | ||||
| chr17:35373614-35373856 | Common:4; Rare:49 | ||||
| chr17:35578515-35578699 | Common:1; Rare:50; Clinvar (benign):1 | ||||
| chr17:36544809-36544961 | Common:2; Rare:50 | ||||
| chr17:36545410-36545654 | Common:2; Rare:76 | ||||
| chr17:37406812-37406935 | Rare:45 | ||||
| chr17:37609362-37609542 | Rare:75 | ||||
| chr17:38428358-38428478 | Common:8; Rare:53 | ||||
| chr17:38825275-38825408 | Common:2; Rare:39 | ||||
| chr17:38853696-38853888 | Common:3; Rare:78 | ||||
| chr17:39193479-39193649 | Rare:37 | ||||
| chr17:39688020-39688078 | Rare:21 | ||||
| chr17:39927499-39927745 | Common:2; Rare:74 | ||||
| chr17:40100590-40100793 | Common:1; Rare:40 |