Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:96208823-96208868 | Common:2; Rare:19 | ||||
chr2:96265978-96266300 | Common:2; Rare:95 | ||||
chr2:98608442-98608699 | Common:1; Rare:106 | ||||
chr2:99154933-99155031 | Common:1; Rare:40 | ||||
chr2:99180977-99181213 | Common:2; Rare:71 | ||||
chr2:100562639-100562959 | Common:5; Rare:85 | ||||
chr2:101002123-101002324 | Rare:74 | ||||
chr2:105337457-105337602 | Common:1; Rare:73 | ||||
chr2:106887255-106887538 | Common:2; Rare:54 | ||||
chr2:108534204-108534504 | Common:7; Rare:123 | ||||
chr2:108719414-108719586 | Common:2; Rare:73; Clinvar (benign):2 | ||||
chr2:110115796-110115948 | Common:2; Rare:36 | ||||
chr2:111884156-111884252 | Rare:26 | ||||
chr2:111898785-111898900 | Common:2; Rare:39; Clinvar (benign):2 | ||||
chr2:112275417-112275594 | Common:1; Rare:49 |