Variant report

Variant rs369980338
Chromosome Location chr2:132983978-132983979
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:132976800-132996200 Weak transcription NHEK skin
2 chr2:132980400-132984000 ZNF genes & repeats hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
3 chr2:132980400-132985400 ZNF genes & repeats HUES48 Cell Line embryonic stem cell
4 chr2:132980400-132985400 ZNF genes & repeats HUES64 Cell Line embryonic stem cell
5 chr2:132980600-132984000 ZNF genes & repeats Fetal Brain Male brain
6 chr2:132982200-132984000 ZNF genes & repeats HUVEC blood vessel
7 chr2:132982800-132984000 ZNF genes & repeats ES-I3 Cell Line embryonic stem cell
8 chr2:132982800-132984000 ZNF genes & repeats Adipose Nuclei Adipose
9 chr2:132982800-132984000 ZNF genes & repeats Liver Liver
10 chr2:132983400-132984000 ZNF genes & repeats K562 blood
11 chr2:132983400-132985000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
12 chr2:132983600-132984000 ZNF genes & repeats HSMMtube muscle
13 chr2:132983600-132984000 ZNF genes & repeats NH-A brain
14 chr2:132983800-132984000 Flanking Active TSS Hela-S3 cervix

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