Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:97645813-97646106 | Common:2; Rare:91 | ||||
chr2:98608421-98608636 | Common:1; Rare:93; Clinvar (benign):1 | ||||
chr2:99141128-99141441 | Common:1; Rare:115 | ||||
chr2:99141512-99141574 | Rare:31 | ||||
chr2:99154873-99155040 | Common:1; Rare:70; Clinvar (benign):2 | ||||
chr2:99180978-99181226 | Common:2; Rare:72 | ||||
chr2:101002172-101002311 | Rare:51 | ||||
chr2:102736844-102736958 | Common:1; Rare:50 | ||||
chr2:105337458-105337620 | Common:1; Rare:77 | ||||
chr2:108449104-108449260 | Rare:54 | ||||
chr2:108534148-108534498 | Common:7; Rare:140 | ||||
chr2:108719388-108719586 | Common:3; Rare:84; Clinvar (benign):2 | ||||
chr2:109613865-109613996 | Common:1; Rare:45 | ||||
chr2:110115802-110115912 | Common:2; Rare:29 | ||||
chr2:110678027-110678212 | Rare:52 |