| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:125719406-125719802 | Common:1; Rare:152 | ||||
| chr10:125823116-125823695 | Common:2; Rare:203; Clinvar:2; Clinvar (benign):2 | ||||
| chr10:125896290-125896568 | Common:2; Rare:15 | ||||
| chr10:126905308-126905453 | Rare:56 | ||||
| chr10:127997949-127998160 | Common:2; Rare:40 | ||||
| chr10:130136327-130136489 | Common:7; Rare:66 | ||||
| chr10:131981864-131982133 | Common:4; Rare:99 | ||||
| chr10:132186748-132187080 | Common:19; Rare:101 | ||||
| chr10:132331786-132332240 | Common:17; Rare:157 | ||||
| chr10:132942545-132942690 | Common:2; Rare:46 | ||||
| chr10:133308821-133309039 | Common:2; Rare:101 | ||||
| chr10:133336867-133337079 | Common:1; Rare:74 | ||||
| chr10:133373336-133373743 | Common:2; Rare:161; Clinvar (benign):1 | ||||
| chr10:133393970-133394316 | Common:2; Rare:152 | ||||
| chr11:207370-207748 | Common:8; Rare:116 |