Variant report

Variant rs73678168
Chromosome Location chr8:49591663-49591664
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:49585200-49592000 Weak transcription Skeletal Muscle Male skeletal muscle
2 chr8:49585400-49592000 Weak transcription Left Ventricle heart
3 chr8:49586200-49591800 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
4 chr8:49586600-49591800 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
5 chr8:49586600-49592000 Weak transcription Primary monocytes fromperipheralblood blood
6 chr8:49586800-49592400 Weak transcription Spleen Spleen
7 chr8:49587000-49591800 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
8 chr8:49587000-49591800 Weak transcription Placenta Amnion Placenta Amnion
9 chr8:49587000-49592200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr8:49587200-49595400 Weak transcription Right Atrium heart
11 chr8:49587800-49595200 Weak transcription Fetal Muscle Leg muscle
12 chr8:49588000-49595200 Weak transcription Fetal Stomach stomach
13 chr8:49588400-49592000 Weak transcription Small Intestine intestine
14 chr8:49590000-49591800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
15 chr8:49590200-49592400 Enhancers Fetal Lung lung
16 chr8:49591200-49592000 Enhancers Fetal Kidney kidney
17 chr8:49591200-49592000 Weak transcription Ovary ovary
18 chr8:49591200-49595400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
19 chr8:49591400-49592400 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
20 chr8:49591600-49592000 Enhancers HUVEC blood vessel
21 chr8:49591600-49592800 Enhancers Fetal Adrenal Gland Adrenal Gland
22 chr8:49591600-49593000 Enhancers HMEC breast

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