| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:132186658-132187058 | Common:49; Rare:296 | ||||
| chr10:132306820-132307200 | Rare:102 | ||||
| chr10:132307841-132308233 | Common:16; Rare:291 | ||||
| chr10:132331758-132332363 | Common:51; Rare:507 | ||||
| chr10:132332429-132333050 | Common:5; Rare:145 | ||||
| chr10:132396170-132396860 | Common:7; Rare:350 | ||||
| chr10:132397046-132397327 | Common:9; Rare:127 | ||||
| chr10:132397367-132397835 | Common:4; Rare:195 | ||||
| chr10:132537242-132537393 | Common:1; Rare:61 | ||||
| chr10:132537302-132538139 | Common:10; Rare:631 | ||||
| chr10:133159600-133160351 | Common:30; Rare:306 | ||||
| chr10:133308745-133308994 | Rare:254 | ||||
| chr10:133309056-133309528 | Common:8; Rare:426 | ||||
| chr10:133373235-133373566 | Common:4; Rare:273; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):6 | ||||
| chr10:133378898-133379335 | Common:55; Rare:202 |