Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:117121695-117121948 | Common:2; Rare:138 | ||||
chr1:117367273-117367531 | Common:9; Rare:163 | ||||
chr1:117605785-117606075 | Rare:90 | ||||
chr1:117929518-117929872 | Common:8; Rare:179 | ||||
chr1:119140584-119140792 | Common:2; Rare:127; Clinvar (pathogenic):1 | ||||
chr1:119648090-119648680 | Common:8; Rare:249 | ||||
chr1:120176356-120176616 | Common:1; Rare:105 | ||||
chr1:145823862-145824301 | Rare:288 | ||||
chr1:145824400-145824700 | Common:1; Rare:107 | ||||
chr1:145845404-145845636 | Common:3; Rare:52 | ||||
chr1:145858996-145859209 | Rare:104 | ||||
chr1:145859630-145860020 | Common:5; Rare:158 | ||||
chr1:145918689-145919022 | Common:4; Rare:139 | ||||
chr1:145926960-145927380 | Common:2; Rare:175; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:145927480-145927679 | Rare:97 |