Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:134485982-134486055 | Common:2; Rare:27 | ||||
chr3:139389568-139389842 | Common:1; Rare:90 | ||||
chr3:142578721-142578963 | Rare:82; Clinvar:1 | ||||
chr3:143001348-143001631 | Common:4; Rare:96 | ||||
chr3:150603204-150603356 | Common:2; Rare:61 | ||||
chr3:156674361-156674618 | Common:3; Rare:73 | ||||
chr3:158802029-158802161 | Common:2; Rare:63 | ||||
chr3:160449748-160450075 | Common:2; Rare:108 | ||||
chr3:179604626-179604827 | Common:1; Rare:65 | ||||
chr3:184135265-184135382 | Common:2; Rare:31; Clinvar:2 | ||||
chr3:184248905-184249021 | Rare:55; Clinvar:4; Clinvar (benign):1 | ||||
chr3:184249489-184249685 | Rare:49 | ||||
chr3:193593130-193593247 | Rare:36 | ||||
chr3:197949894-197950240 | Common:4; Rare:106; Clinvar (benign):2 | ||||
chr4:499132-499257 | Common:3; Rare:42 |