| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:8045618-8046131 | Common:6; Rare:203 | ||||
| chr10:8046824-8046924 | Common:1; Rare:28 | ||||
| chr10:8048336-8048736 | Common:8; Rare:179 | ||||
| chr10:8048744-8049051 | Common:4; Rare:159 | ||||
| chr10:8049023-8049455 | Common:4; Rare:136 | ||||
| chr10:8049428-8049963 | Common:15; Rare:237 | ||||
| chr10:8050410-8050954 | Common:13; Rare:373 | ||||
| chr10:8050954-8051322 | Common:10; Rare:265 | ||||
| chr10:8051690-8052375 | Common:15; Rare:399 | ||||
| chr10:8056309-8057293 | Common:14; Rare:454 | ||||
| chr10:8059933-8060727 | Common:15; Rare:320 | ||||
| chr10:8061264-8061560 | Common:7; Rare:118 | ||||
| chr10:8061731-8062470 | Common:35; Rare:391 | ||||
| chr10:8062936-8063213 | Common:2; Rare:87 | ||||
| chr10:8063821-8064422 | Common:12; Rare:147; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):6 |