Variant report

Variant rs4930994
Chromosome Location chr12:32000892-32000893
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:7 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:31996400-32004400 ZNF genes & repeats hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
2 chr12:32000200-32001400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr12:32000600-32002400 ZNF genes & repeats Primary B cells from cord blood blood
4 chr12:32000800-32001000 ZNF genes & repeats Thymus Thymus
5 chr12:32000800-32001400 ZNF genes & repeats Adipose Nuclei Adipose
6 chr12:32000800-32002000 ZNF genes & repeats ES-UCSF4 Cell Line embryonic stem cell
7 chr12:32000800-32004000 ZNF genes & repeats iPS-20b Cell Line embryonic stem cell

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