Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:27771699-27771995 | Common:1; Rare:96 | ||||
chr2:27890420-27890822 | Rare:103 | ||||
chr2:28751702-28752165 | Common:2; Rare:190 | ||||
chr2:28870273-28870437 | Rare:57 | ||||
chr2:28894354-28894717 | Common:5; Rare:122 | ||||
chr2:32010963-32011167 | Rare:61 | ||||
chr2:32039761-32039906 | Rare:49 | ||||
chr2:32165735-32165898 | Common:1; Rare:61 | ||||
chr2:32277788-32277972 | Common:1; Rare:45 | ||||
chr2:33599210-33599432 | Common:1; Rare:86 | ||||
chr2:37084312-37084561 | Common:3; Rare:94 | ||||
chr2:37231551-37231702 | Common:4; Rare:85; Clinvar (benign):3 | ||||
chr2:37671592-37671745 | Common:1; Rare:72 | ||||
chr2:38875902-38876059 | Common:1; Rare:54 | ||||
chr2:39437104-39437456 | Common:4; Rare:124 |