Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:46973592-46973789 | Rare:89 | ||||
chr16:47461032-47461343 | Common:2; Rare:110; Clinvar (benign):1 | ||||
chr16:53099120-53099180 | Rare:14 | ||||
chr16:53703821-53704179 | Rare:101; Clinvar:3; Clinvar (benign):1 | ||||
chr16:56451312-56451573 | Common:1; Rare:73 | ||||
chr16:56682346-56682482 | Common:3; Rare:46 | ||||
chr16:57186001-57186335 | Common:1; Rare:98 | ||||
chr16:57244964-57245185 | Common:3; Rare:76 | ||||
chr16:57447360-57447517 | Common:2; Rare:43; Clinvar:2; Clinvar (benign):1 | ||||
chr16:57480359-57480476 | Rare:23 | ||||
chr16:58001318-58001429 | Rare:26 | ||||
chr16:58129289-58129573 | Common:2; Rare:88 | ||||
chr16:66552461-66552654 | Rare:83 | ||||
chr16:66934360-66934499 | Common:1; Rare:51 | ||||
chr16:67226843-67227167 | Common:1; Rare:113 |