Variant report

Variant rs10129329
Chromosome Location chr14:37694022-37694023
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:37676000-37695600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr14:37676600-37699400 Weak transcription A549 lung
3 chr14:37681000-37694200 Weak transcription Pancreas Pancrea
4 chr14:37682000-37695800 Weak transcription Gastric stomach
5 chr14:37684200-37694200 Weak transcription Aorta Aorta
6 chr14:37691000-37694200 Weak transcription Ovary ovary
7 chr14:37693200-37694200 ZNF genes & repeats hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
8 chr14:37693200-37694200 ZNF genes & repeats HUES64 Cell Line embryonic stem cell
9 chr14:37693200-37694200 ZNF genes & repeats iPS-20b Cell Line embryonic stem cell
10 chr14:37693400-37694200 ZNF genes & repeats HUES6 Cell Line embryonic stem cell
11 chr14:37693400-37694600 ZNF genes & repeats H1 Cell Line embryonic stem cell
12 chr14:37693600-37694800 ZNF genes & repeats Foreskin Keratinocyte Primary Cells skin03 Skin
13 chr14:37693800-37695000 ZNF genes & repeats Breast Myoepithelial Primary Cells Breast
14 chr14:37694000-37695400 ZNF genes & repeats H1 Derived Mesenchymal Stem Cells ES cell derived
15 chr14:37694000-37696600 Weak transcription Stomach Mucosa stomach

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