Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:38875902-38876064 | Common:1; Rare:56 | ||||
chr2:39437086-39437453 | Common:4; Rare:131 | ||||
chr2:43595978-43596191 | Common:1; Rare:69 | ||||
chr2:44361766-44362020 | Common:2; Rare:77 | ||||
chr2:46617025-46617262 | Common:7; Rare:103 | ||||
chr2:46915722-46915908 | Common:1; Rare:56; Clinvar:2; Clinvar (benign):1 | ||||
chr2:47176441-47176569 | Rare:93; Clinvar (benign):5 | ||||
chr2:48440619-48440858 | Common:8; Rare:113 | ||||
chr2:48529242-48529386 | Common:1; Rare:39 | ||||
chr2:53786856-53787090 | Rare:81 | ||||
chr2:53970788-53971126 | Common:10; Rare:113 | ||||
chr2:55050441-55050763 | Common:4; Rare:96 | ||||
chr2:55232249-55232414 | Common:3; Rare:39 | ||||
chr2:55519328-55519651 | Rare:101 | ||||
chr2:58046755-58046836 | Rare:29 |