Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:70221203-70221707 | Rare:846 | ||||
chr1:70221693-70222093 | Rare:221 | ||||
chr1:70250004-70250626 | Common:1; Rare:212 | ||||
chr1:70354580-70354936 | Common:1; Rare:445 | ||||
chr1:70354900-70355240 | Common:4; Rare:270 | ||||
chr1:70410635-70410867 | Common:1; Rare:60 | ||||
chr1:70410953-70411360 | Common:16; Rare:483; Clinvar:6; Clinvar (benign):6 | ||||
chr1:71046780-71047632 | Common:5; Rare:384 | ||||
chr1:71047655-71048055 | Common:10; Rare:275 | ||||
chr1:71080446-71080846 | Common:3; Rare:120 | ||||
chr1:71080956-71081510 | Common:2; Rare:809 | ||||
chr1:71081769-71082169 | Common:2; Rare:85 | ||||
chr1:74197516-74197916 | Rare:69 | ||||
chr1:74197990-74198979 | Common:22; Rare:1033 | ||||
chr1:74732930-74733337 | Common:37; Rare:690 |