| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:7943632-7943990 | Rare:100 | ||||
| chr19:8005510-8005821 | Common:1; Rare:109 | ||||
| chr19:8308271-8308639 | Common:3; Rare:121; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:8321321-8321703 | Common:2; Rare:154 | ||||
| chr19:8363970-8364159 | Common:1; Rare:45 | ||||
| chr19:8390042-8390449 | Common:2; Rare:115 | ||||
| chr19:8514145-8514222 | Common:1; Rare:22 | ||||
| chr19:9435503-9435602 | Rare:40 | ||||
| chr19:9538563-9538741 | Common:1; Rare:57 | ||||
| chr19:9621162-9621555 | Common:4; Rare:113 | ||||
| chr19:9675022-9675155 | Rare:36 | ||||
| chr19:9700670-9700860 | Common:2; Rare:36 | ||||
| chr19:9768565-9768762 | Common:2; Rare:70 | ||||
| chr19:9818792-9818841 | Rare:15 | ||||
| chr19:9827635-9827963 | Common:2; Rare:91 |