Variant report

Variant rs73624803
Chromosome Location chr19:37672386-37672387
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:37663600-37673200 Weak transcription Placenta Amnion Placenta Amnion
2 chr19:37664000-37673000 Weak transcription Fetal Brain Female brain
3 chr19:37664000-37673400 Weak transcription Fetal Brain Male brain
4 chr19:37664200-37673200 Weak transcription Fetal Heart heart
5 chr19:37664200-37675400 Weak transcription ES-I3 Cell Line embryonic stem cell
6 chr19:37668000-37686000 ZNF genes & repeats Liver Liver
7 chr19:37670000-37681200 ZNF genes & repeats Adipose Nuclei Adipose
8 chr19:37670400-37672800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
9 chr19:37672000-37674800 ZNF genes & repeats Primary T killer memory cells from peripheral blood blood
10 chr19:37672000-37676000 ZNF genes & repeats Duodenum Smooth Muscle Duodenum
11 chr19:37672000-37686400 ZNF genes & repeats Monocytes-CD14+_RO01746 blood
12 chr19:37672200-37674800 ZNF genes & repeats Duodenum Mucosa Duodenum
13 chr19:37672200-37675200 ZNF genes & repeats Primary T helper cells fromperipheralblood blood
14 chr19:37672200-37676000 ZNF genes & repeats Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
15 chr19:37672200-37686000 ZNF genes & repeats Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived

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