Variant report

Variant rs1866531
Chromosome Location chr1:242481631-242481632
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:242472600-242485400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
2 chr1:242477800-242485400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr1:242481200-242481800 Enhancers Fetal Brain Male brain
4 chr1:242481400-242481800 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
5 chr1:242481400-242481800 ZNF genes & repeats Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr1:242481400-242481800 Enhancers Aorta Aorta
7 chr1:242481400-242481800 Enhancers HMEC breast
8 chr1:242481400-242482000 Enhancers Breast Myoepithelial Primary Cells Breast
9 chr1:242481400-242482000 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
10 chr1:242481600-242481800 ZNF genes & repeats H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived

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