Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:179954675-179954834 | Common:1; Rare:35 | ||||
chr1:180502357-180502647 | Common:1; Rare:100 | ||||
chr1:180631861-180632196 | Common:5; Rare:121 | ||||
chr1:180940877-180941165 | Common:8; Rare:89 | ||||
chr1:181088494-181088711 | Rare:71 | ||||
chr1:182388682-182388827 | Rare:36 | ||||
chr1:182388840-182389032 | Common:2; Rare:43 | ||||
chr1:182390087-182390116 | Rare:1 | ||||
chr1:182391273-182391446 | Rare:37 | ||||
chr1:182391679-182392068 | Common:5; Rare:144; Clinvar:6; Clinvar (benign):5 | ||||
chr1:182589182-182589323 | Rare:30 | ||||
chr1:182604357-182604519 | Rare:36 | ||||
chr1:182671753-182671963 | Common:3; Rare:46 | ||||
chr1:182789620-182789796 | Common:2; Rare:62 | ||||
chr1:182839095-182839422 | Common:1; Rare:123 |