| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:46698640-46698998 | Common:7; Rare:241 | ||||
| chr2:46699010-46699890 | Common:10; Rare:496 | ||||
| chr2:46915688-46916054 | Common:7; Rare:300; Clinvar:8; Clinvar (benign):3 | ||||
| chr2:46915970-46916250 | Common:5; Rare:180 | ||||
| chr2:46940998-46941917 | Common:21; Rare:701; Clinvar:5; Clinvar (benign):8 | ||||
| chr2:46942267-46942447 | Common:5; Rare:61 | ||||
| chr2:47176213-47177003 | Common:18; Rare:730; Clinvar (benign):10 | ||||
| chr2:47344959-47345367 | Common:4; Rare:220 | ||||
| chr2:47369114-47369702 | Common:13; Rare:561; Clinvar:43; Clinvar (benign):16 | ||||
| chr2:47402872-47403413 | Common:4; Rare:540; Clinvar:194; Clinvar (benign):121; Clinvar (pathogenic):9 | ||||
| chr2:47570815-47571215 | Common:8; Rare:342 | ||||
| chr2:47782869-47783239 | Common:7; Rare:412; Clinvar:21; Clinvar (benign):49; Clinvar (pathogenic):1 | ||||
| chr2:47783705-47784025 | Common:19; Rare:168; Clinvar (benign):4 | ||||
| chr2:47905220-47905545 | Common:6; Rare:268 | ||||
| chr2:47905540-47905960 | Common:3; Rare:312 |