Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:32674102-32674247 | Common:1; Rare:23 | ||||
chr1:35577758-35577835 | Rare:21 | ||||
chr1:41168225-41168494 | Rare:50 | ||||
chr1:42929678-42930046 | Common:2; Rare:94; Clinvar:5; Clinvar (benign):15; Clinvar (pathogenic):5 | ||||
chr1:42955067-42955267 | Rare:29 | ||||
chr1:46804188-46804478 | Common:3; Rare:44 | ||||
chr1:46813915-46814324 | Common:4; Rare:136 | ||||
chr1:46854596-46854798 | Common:1; Rare:43 | ||||
chr1:46857825-46857886 | Common:1; Rare:7 | ||||
chr1:46862149-46862398 | Common:3; Rare:40 | ||||
chr1:46885119-46885382 | Common:4; Rare:37 | ||||
chr1:46897536-46897800 | Common:1; Rare:28 | ||||
chr1:51790627-51790864 | Common:2; Rare:60 | ||||
chr1:51790964-51791224 | Common:1; Rare:62 | ||||
chr1:52919900-52920112 | Rare:26 |