Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:37925174-37925317 | Rare:55 | ||||
chr2:38602895-38603193 | Common:4; Rare:117 | ||||
chr2:38665804-38666124 | Common:3; Rare:79 | ||||
chr2:38751335-38751430 | Rare:50 | ||||
chr2:38875906-38876040 | Common:1; Rare:41 | ||||
chr2:39120998-39121114 | Rare:36 | ||||
chr2:42169044-42169496 | Common:1; Rare:180 | ||||
chr2:42568079-42568265 | Rare:49 | ||||
chr2:43595957-43596057 | Common:1; Rare:41 | ||||
chr2:44361756-44362005 | Common:1; Rare:76 | ||||
chr2:46617022-46617285 | Common:7; Rare:112 | ||||
chr2:46915733-46915908 | Common:1; Rare:52; Clinvar:2; Clinvar (benign):1 | ||||
chr2:46941722-46941874 | Common:3; Rare:46 | ||||
chr2:47176443-47176606 | Rare:113; Clinvar (benign):5 | ||||
chr2:47695289-47695550 | Common:2; Rare:44 |