Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:220102225-220102274 | Rare:7 | ||||
chr2:221443333-221443567 | Common:3; Rare:53 | ||||
chr2:222319024-222319326 | Common:1; Rare:57 | ||||
chr2:223944364-223944523 | Common:1; Rare:40 | ||||
chr2:226797436-226797638 | Common:1; Rare:60 | ||||
chr2:226798755-226798816 | Rare:17 | ||||
chr2:226898876-226899008 | Rare:17 | ||||
chr2:230066924-230067217 | Common:1; Rare:65 | ||||
chr2:230885897-230886179 | Common:5; Rare:48 | ||||
chr2:231514211-231514616 | Common:6; Rare:150 | ||||
chr2:231604585-231604957 | Common:21; Rare:130 | ||||
chr2:234495954-234495957 | |||||
chr2:238231700-238231726 | Rare:12 | ||||
chr2:240762569-240762758 | Rare:41; Clinvar:1; Clinvar (benign):3 | ||||
chr2:240821338-240821502 | Rare:29 |