Variant report

Variant rs11991678
Chromosome Location chr8:10450497-10450498
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:10439000-10453000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
2 chr8:10447800-10452000 Bivalent Enhancer Fetal Muscle Trunk muscle
3 chr8:10448200-10450800 Weak transcription Hela-S3 cervix
4 chr8:10448200-10451000 Weak transcription NH-A brain
5 chr8:10448200-10451400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
6 chr8:10448200-10456200 Weak transcription Liver Liver
7 chr8:10449000-10454600 Weak transcription Spleen Spleen
8 chr8:10449600-10453800 Enhancers Primary neutrophils fromperipheralblood blood
9 chr8:10450000-10451400 Bivalent Enhancer Skeletal Muscle Male skeletal muscle
10 chr8:10450000-10452000 Enhancers Brain Anterior Caudate brain
11 chr8:10450200-10452000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
12 chr8:10450400-10450600 Enhancers H1 Cell Line embryonic stem cell
13 chr8:10450400-10450600 Bivalent Enhancer hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
14 chr8:10450400-10450600 Enhancers HUES6 Cell Line embryonic stem cell
15 chr8:10450400-10450600 Enhancers Lung lung
16 chr8:10450400-10450600 Bivalent Enhancer Stomach Smooth Muscle stomach
17 chr8:10450400-10451200 Enhancers Brain Hippocampus Middle brain
18 chr8:10450400-10451600 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
19 chr8:10450400-10451600 Enhancers Brain Inferior Temporal Lobe brain

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