Variant report

Variant rs6901219
Chromosome Location chr6:146043652-146043653
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:146006800-146050000 Weak transcription Brain Cingulate Gyrus brain
2 chr6:146007400-146043800 Weak transcription Liver Liver
3 chr6:146026800-146055800 Weak transcription Left Ventricle heart
4 chr6:146028600-146049200 Weak transcription Stomach Smooth Muscle stomach
5 chr6:146030200-146054000 Weak transcription Skeletal Muscle Male skeletal muscle
6 chr6:146035800-146055200 Weak transcription Brain Inferior Temporal Lobe brain
7 chr6:146036200-146044200 Weak transcription HUES64 Cell Line embryonic stem cell
8 chr6:146036200-146049800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr6:146036200-146054800 Weak transcription Skeletal Muscle Female skeletal muscle
10 chr6:146036600-146044600 Weak transcription Brain Hippocampus Middle brain
11 chr6:146036800-146050000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
12 chr6:146036800-146050000 Weak transcription Thymus Thymus
13 chr6:146037000-146052000 Weak transcription Ovary ovary
14 chr6:146037800-146044800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
15 chr6:146038400-146052600 Weak transcription Fetal Heart heart
16 chr6:146041400-146043800 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
17 chr6:146041800-146050000 Weak transcription Fetal Stomach stomach
18 chr6:146042000-146044800 Weak transcription Primary B cells from cord blood blood
19 chr6:146043600-146044000 ZNF genes & repeats Primary T cells from cord blood blood

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