The 2.0 version of rSNPBase

Variant report

Variant rs28494034
Chromosome Location chr14:32368598-32368599
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:32364200-32371200 Weak transcription Placenta Placenta
2 chr14:32364400-32371000 Weak transcription HUES6 Cell Line embryonic stem cell
3 chr14:32364800-32370400 Weak transcription K562 blood
4 chr14:32364800-32371000 Weak transcription ES-I3 Cell Line embryonic stem cell
5 chr14:32365200-32370800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr14:32365200-32370800 Weak transcription NHEK skin
7 chr14:32366200-32369000 Enhancers Primary B cells from peripheral blood blood
8 chr14:32367000-32368800 Enhancers Primary monocytes fromperipheralblood blood
9 chr14:32367200-32368800 Enhancers Primary B cells from cord blood blood
10 chr14:32367200-32370000 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
11 chr14:32367200-32370200 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
12 chr14:32367200-32370800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr14:32367200-32376200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
14 chr14:32368000-32368600 Enhancers HMEC breast
15 chr14:32368000-32368600 Enhancers Monocytes-CD14+_RO01746 blood
16 chr14:32368400-32370400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin

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Last update: Aug 31, 2015