Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:94820186-94820420 | Common:3; Rare:62 | ||||
chr1:94927022-94927405 | Common:3; Rare:128 | ||||
chr1:95072855-95072995 | Common:1; Rare:58; Clinvar (benign):2 | ||||
chr1:95117288-95117577 | Common:1; Rare:85 | ||||
chr1:95233945-95234247 | Common:5; Rare:93 | ||||
chr1:98661587-98661887 | Common:2; Rare:104 | ||||
chr1:99646017-99646324 | Rare:63 | ||||
chr1:99850005-99850200 | Common:1; Rare:72 | ||||
chr1:99850337-99850425 | Rare:29; Clinvar:2; Clinvar (benign):1 | ||||
chr1:99969633-99969770 | Common:1; Rare:26 | ||||
chr1:99969843-99970069 | Rare:51 | ||||
chr1:100038001-100038171 | Common:1; Rare:69 | ||||
chr1:100132814-100133251 | Common:3; Rare:176 | ||||
chr1:100249790-100250063 | Common:4; Rare:92; Clinvar:1; Clinvar (benign):1 | ||||
chr1:100266107-100266418 | Common:4; Rare:110 |