Variant report

Variant rs9386818
Chromosome Location chr6:109901656-109901657
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:109878800-109903600 Weak transcription Psoas Muscle Psoas
2 chr6:109879000-109903800 Weak transcription Thymus Thymus
3 chr6:109879000-109906000 Weak transcription Left Ventricle heart
4 chr6:109879000-109917400 Weak transcription Aorta Aorta
5 chr6:109881200-109902400 Weak transcription Primary T helper cells fromperipheralblood blood
6 chr6:109885000-109902400 Weak transcription Skeletal Muscle Male skeletal muscle
7 chr6:109886000-109910600 Weak transcription Primary B cells from cord blood blood
8 chr6:109899200-109901800 Weak transcription Brain Inferior Temporal Lobe brain
9 chr6:109900600-109902400 Weak transcription Adipose Nuclei Adipose
10 chr6:109900600-109902400 Weak transcription Skeletal Muscle Female skeletal muscle
11 chr6:109900800-109906000 Weak transcription Primary Natural Killer cells fromperipheralblood blood
12 chr6:109901400-109902200 Enhancers iPS-20b Cell Line embryonic stem cell
13 chr6:109901600-109902000 Enhancers ES-UCSF4 Cell Line embryonic stem cell
14 chr6:109901600-109902200 Enhancers HUES64 Cell Line embryonic stem cell
15 chr6:109901600-109902400 Enhancers iPS-15b Cell Line embryonic stem cell
16 chr6:109901600-109902400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
17 chr6:109901600-109902400 Strong transcription Primary T cells from cord blood blood

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