Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:217834209-217834498 | Common:1; Rare:51 | ||||
chr2:217910135-217910385 | Common:2; Rare:37 | ||||
chr2:217993135-217993397 | Common:4; Rare:38 | ||||
chr2:218033945-218034051 | Rare:27 | ||||
chr2:218272454-218272635 | Common:1; Rare:57 | ||||
chr2:218277366-218277578 | Rare:64 | ||||
chr2:218277631-218277731 | Rare:20 | ||||
chr2:218402634-218402714 | Rare:25 | ||||
chr2:222319028-222319339 | Common:1; Rare:59 | ||||
chr2:223944343-223944496 | Common:1; Rare:40 | ||||
chr2:226796085-226796258 | Rare:64 | ||||
chr2:226796273-226796302 | Common:1; Rare:16; Clinvar (benign):1 | ||||
chr2:226796826-226797120 | Rare:87; Clinvar (pathogenic):1 | ||||
chr2:226798863-226799163 | Common:2; Rare:74 | ||||
chr2:231190981-231191033 | Common:1; Rare:13 |