| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:6361485-6361853 | Common:1; Rare:143; Clinvar:2; Clinvar (benign):5 | ||||
| chr19:6372505-6372910 | Common:5; Rare:142 | ||||
| chr19:6373219-6373557 | Common:2; Rare:55 | ||||
| chr19:6381123-6381383 | Common:3; Rare:103 | ||||
| chr19:6393119-6393600 | Common:5; Rare:138 | ||||
| chr19:6393634-6393773 | Common:1; Rare:40 | ||||
| chr19:6393965-6394034 | Rare:19 | ||||
| chr19:6415602-6415935 | Common:4; Rare:139 | ||||
| chr19:6416825-6417086 | Common:1; Rare:89 | ||||
| chr19:6424513-6424771 | Common:3; Rare:74 | ||||
| chr19:6685105-6685407 | Common:2; Rare:65; Clinvar:1 | ||||
| chr19:6686809-6687064 | Rare:52 | ||||
| chr19:6720647-6720821 | Common:2; Rare:37 | ||||
| chr19:6737212-6737359 | Common:2; Rare:39 | ||||
| chr19:6737493-6737939 | Common:7; Rare:136 |