| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144852979-144853149 | Rare:64 | ||||
| chr8:144901412-144901727 | Common:1; Rare:89 | ||||
| chr9:2844049-2844355 | Common:5; Rare:118 | ||||
| chr9:4662207-4662386 | Common:4; Rare:73 | ||||
| chr9:4679444-4679701 | Rare:113 | ||||
| chr9:4741145-4741373 | Common:3; Rare:103 | ||||
| chr9:12775238-12775311 | Common:1; Rare:15 | ||||
| chr9:12775959-12776002 | Rare:18 | ||||
| chr9:16870657-16870836 | Rare:87 | ||||
| chr9:19049326-19049473 | Rare:68 | ||||
| chr9:19380205-19380383 | Common:5; Rare:85 | ||||
| chr9:21994186-21994520 | Rare:123; Clinvar:16; Clinvar (benign):15; Clinvar (pathogenic):2 | ||||
| chr9:21994593-21994823 | Common:1; Rare:61 | ||||
| chr9:21994937-21995104 | Common:1; Rare:27 | ||||
| chr9:33025093-33025285 | Common:5; Rare:78 |