Variant report

Variant rs1327993
Chromosome Location chr6:4301551-4301552
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:4298200-4301800 Weak transcription Placenta Placenta
2 chr6:4300200-4304400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr6:4300200-4304400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr6:4300200-4316800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr6:4300400-4302000 Weak transcription Primary monocytes fromperipheralblood blood
6 chr6:4300400-4302000 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
7 chr6:4300600-4301800 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
8 chr6:4300600-4302000 Weak transcription Fetal Adrenal Gland Adrenal Gland
9 chr6:4300600-4302200 Enhancers Fetal Intestine Large intestine
10 chr6:4300800-4301600 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
11 chr6:4301400-4302000 Enhancers Skeletal Muscle Male skeletal muscle
12 chr6:4301400-4302800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr6:4301400-4303000 Enhancers Fetal Muscle Leg muscle
14 chr6:4301400-4303000 Enhancers Left Ventricle heart
15 chr6:4301400-4303200 Enhancers Skeletal Muscle Female skeletal muscle

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