Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:179081909-179082119 | Common:1; Rare:68 | ||||
chr1:179293561-179293919 | Common:3; Rare:112 | ||||
chr1:179882123-179882415 | Common:1; Rare:55 | ||||
chr1:179882488-179882945 | Common:1; Rare:227; Clinvar:9; Clinvar (benign):4 | ||||
chr1:179883007-179883168 | Common:3; Rare:61 | ||||
chr1:179954700-179954817 | Rare:26 | ||||
chr1:180154703-180154920 | Common:1; Rare:82 | ||||
chr1:181033265-181033401 | Common:1; Rare:17 | ||||
chr1:181088563-181088722 | Rare:59 | ||||
chr1:182391286-182391429 | Rare:29 | ||||
chr1:182391679-182392034 | Common:5; Rare:128; Clinvar:5; Clinvar (benign):5 | ||||
chr1:182789664-182789805 | Common:2; Rare:54 | ||||
chr1:183022994-183023279 | Common:6; Rare:77 | ||||
chr1:183186111-183186335 | Common:3; Rare:46; Clinvar:1; Clinvar (benign):3 | ||||
chr1:183472258-183472528 | Common:2; Rare:94 |