Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:215049729-215049910 | Common:1; Rare:52; Clinvar (benign):1 | ||||
chr2:215072252-215072370 | Rare:20 | ||||
chr2:215294104-215294239 | Common:1; Rare:24 | ||||
chr2:218264499-218264802 | Rare:74 | ||||
chr2:218272436-218272748 | Common:2; Rare:105; Clinvar (benign):1 | ||||
chr2:218276024-218276154 | Rare:36 | ||||
chr2:218404146-218404345 | Rare:51 | ||||
chr2:224364358-224364620 | Common:2; Rare:45 | ||||
chr2:226795793-226795937 | Common:1; Rare:41; Clinvar:1 | ||||
chr2:231614191-231614380 | Common:3; Rare:49 | ||||
chr2:231642693-231642966 | Common:2; Rare:62 | ||||
chr2:231712104-231712407 | Common:1; Rare:97 | ||||
chr2:238282490-238282688 | Rare:40 | ||||
chr2:238286714-238286836 | Rare:20 | ||||
chr2:238287620-238287897 | Rare:55 |