| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:13156485-13156614 | Rare:34 | ||||
| chr19:13156957-13157188 | Rare:41 | ||||
| chr19:13157829-13157878 | Rare:12 | ||||
| chr19:13162730-13163053 | Rare:66 | ||||
| chr19:13163056-13163548 | Common:3; Rare:123 | ||||
| chr19:13163736-13163787 | Rare:6 | ||||
| chr19:13167659-13167984 | Common:2; Rare:75 | ||||
| chr19:13207967-13208021 | Common:1; Rare:11; Clinvar (benign):1 | ||||
| chr19:13208223-13208489 | Common:2; Rare:64 | ||||
| chr19:13208610-13208777 | Rare:63; Clinvar:2; Clinvar (benign):2 | ||||
| chr19:13209390-13209748 | Common:5; Rare:78; Clinvar:7; Clinvar (benign):5 | ||||
| chr19:13209762-13209788 | Rare:6 | ||||
| chr19:13215670-13215798 | Common:1; Rare:27 | ||||
| chr19:13261157-13261391 | Rare:40 | ||||
| chr19:13789275-13789327 | Rare:15 |