Variant report

Variant rs2844667
Chromosome Location chr6:30974337-30974338
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:30965200-30975800 Weak transcription Gastric stomach
2 chr6:30970600-30978000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr6:30971200-30974800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr6:30972400-30974400 Enhancers Skeletal Muscle Male skeletal muscle
5 chr6:30972600-30975000 Weak transcription Left Ventricle heart
6 chr6:30972600-30975200 Weak transcription NHEK skin
7 chr6:30972600-30975400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr6:30972600-30997600 Weak transcription Right Atrium heart
9 chr6:30973200-30975000 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
10 chr6:30973400-30975000 Weak transcription HMEC breast
11 chr6:30973400-30976000 Weak transcription Skeletal Muscle Female skeletal muscle
12 chr6:30973600-30975600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr6:30974000-30976200 Enhancers H9 Derived Neuron Cultured Cells ES cell derived

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