Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:209675145-209675457 | Common:2; Rare:78 | ||||
chr1:211326747-211326874 | Common:3; Rare:30 | ||||
chr1:212035513-212035793 | Common:2; Rare:71 | ||||
chr1:212608448-212608767 | Common:1; Rare:80 | ||||
chr1:212791754-212791934 | Common:3; Rare:76 | ||||
chr1:214602906-214603227 | Common:2; Rare:87 | ||||
chr1:217631026-217631381 | Common:2; Rare:101 | ||||
chr1:218346734-218346932 | Rare:50; Clinvar:7; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:219173796-219173919 | Common:1; Rare:71 | ||||
chr1:221742072-221742286 | Rare:58 | ||||
chr1:222589871-222589934 | Common:2; Rare:19 | ||||
chr1:222617826-222618108 | Common:3; Rare:68 | ||||
chr1:222644114-222644386 | Common:2; Rare:80 | ||||
chr1:222712459-222712582 | Rare:45 | ||||
chr1:222713243-222713408 | Common:1; Rare:50 |