Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:87818211-87818286 | Rare:22 | ||||
chr10:89414481-89414759 | Common:3; Rare:94 | ||||
chr10:89701409-89701611 | Common:1; Rare:56 | ||||
chr10:94545704-94545837 | Common:2; Rare:43 | ||||
chr10:95290990-95291196 | Common:2; Rare:89 | ||||
chr10:97426122-97426263 | Common:1; Rare:56 | ||||
chr10:97445983-97446221 | Rare:61 | ||||
chr10:99430622-99430923 | Common:3; Rare:68 | ||||
chr10:99732093-99732321 | Rare:78; Clinvar:3 | ||||
chr10:100987441-100987564 | Common:1; Rare:49; Clinvar (benign):1 | ||||
chr10:101588224-101588329 | Rare:44 | ||||
chr10:102714278-102714627 | Common:2; Rare:117 | ||||
chr10:103396411-103396686 | Rare:98 | ||||
chr10:103917778-103917872 | Rare:19 | ||||
chr10:112446904-112447252 | Common:3; Rare:84 |