Variant report

Variant rs397886283
Chromosome Location chr6:167263700-167263701
allele -/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:167249000-167272200 Weak transcription Fetal Stomach stomach
2 chr6:167251200-167266000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr6:167251800-167272800 Weak transcription Stomach Smooth Muscle stomach
4 chr6:167253000-167265400 Weak transcription Brain Anterior Caudate brain
5 chr6:167260400-167274400 Weak transcription Breast Myoepithelial Primary Cells Breast
6 chr6:167262000-167264400 Enhancers Primary B cells from peripheral blood blood
7 chr6:167262000-167264600 Weak transcription Brain Cingulate Gyrus brain
8 chr6:167262000-167275000 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
9 chr6:167262200-167265400 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
10 chr6:167262600-167263800 Enhancers Primary B cells from cord blood blood
11 chr6:167262600-167265400 Weak transcription Brain Hippocampus Middle brain
12 chr6:167262600-167266000 Weak transcription Primary T helper 17 cells PMA-I stimulated --
13 chr6:167262600-167267200 Enhancers Fetal Brain Male brain
14 chr6:167263000-167263800 Weak transcription Pancreas Pancrea
15 chr6:167263200-167263800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
16 chr6:167263200-167266000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
17 chr6:167263600-167265600 Weak transcription GM12878-XiMat blood

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