| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:9645088-9645488 | Common:7; Rare:173 | ||||
| chr17:9645880-9646280 | Common:5; Rare:96 | ||||
| chr17:10026150-10026600 | Common:1; Rare:81 | ||||
| chr17:10198581-10198716 | Common:1; Rare:39 | ||||
| chr17:10198790-10199050 | Common:2; Rare:83 | ||||
| chr17:10549070-10549410 | Common:1; Rare:51 | ||||
| chr17:10697505-10697696 | Common:4; Rare:71; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:10697944-10698073 | Common:1; Rare:31 | ||||
| chr17:10729835-10730291 | Common:17; Rare:191 | ||||
| chr17:11598306-11598518 | Common:4; Rare:58 | ||||
| chr17:11598890-11599170 | Common:3; Rare:85 | ||||
| chr17:11996845-11997032 | Rare:46 | ||||
| chr17:11997354-11997636 | Common:3; Rare:111 | ||||
| chr17:12020687-12020886 | Common:2; Rare:85 | ||||
| chr17:12665630-12666030 | Common:5; Rare:143 |