Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:178725136-178725392 | Common:10; Rare:86 | ||||
chr1:178869196-178869332 | Common:1; Rare:23 | ||||
chr1:178870977-178871287 | Rare:61 | ||||
chr1:179294086-179294177 | Rare:18 | ||||
chr1:179365691-179365961 | Common:6; Rare:61 | ||||
chr1:179881927-179882438 | Common:4; Rare:119 | ||||
chr1:179882523-179882682 | Rare:83; Clinvar:2; Clinvar (benign):2 | ||||
chr1:179882684-179882945 | Common:1; Rare:130; Clinvar:7; Clinvar (benign):2 | ||||
chr1:179883001-179883037 | Common:3; Rare:12 | ||||
chr1:179954669-179954826 | Common:1; Rare:35 | ||||
chr1:179954849-179955135 | Common:1; Rare:59 | ||||
chr1:180154669-180155023 | Common:6; Rare:124 | ||||
chr1:181033265-181033387 | Common:1; Rare:17 | ||||
chr1:181088494-181088721 | Rare:77 | ||||
chr1:182391308-182391444 | Rare:27 |