Variant report

Variant rs12431694
Chromosome Location chr14:66257012-66257013
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:66256200-66257200 Bivalent Enhancer H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr14:66256200-66257200 Enhancers Fetal Brain Male brain
3 chr14:66256200-66257400 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
4 chr14:66256400-66257200 Bivalent Enhancer Fetal Muscle Trunk muscle
5 chr14:66256400-66258200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
6 chr14:66256400-66258200 Weak transcription Spleen Spleen
7 chr14:66256400-66259200 Enhancers H1 Cell Line embryonic stem cell
8 chr14:66256600-66257600 Enhancers HUES6 Cell Line embryonic stem cell
9 chr14:66256600-66257600 Enhancers Brain Germinal Matrix brain
10 chr14:66256600-66260200 Enhancers Primary Natural Killer cells fromperipheralblood blood
11 chr14:66256800-66257200 Bivalent Enhancer HepG2 liver
12 chr14:66256800-66258200 Weak transcription Fetal Lung lung
13 chr14:66257000-66257200 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
14 chr14:66257000-66257400 Enhancers H9 Cell Line embryonic stem cell
15 chr14:66257000-66257400 Bivalent Enhancer H9 Derived Neuron Cultured Cells ES cell derived
16 chr14:66257000-66257600 Enhancers ES-UCSF4 Cell Line embryonic stem cell

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