Variant report

Variant rs2291158
Chromosome Location chr12:10225855-10225856
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:10219000-10236800 Weak transcription Left Ventricle heart
2 chr12:10220800-10234800 Weak transcription Placenta Placenta
3 chr12:10221400-10235000 Weak transcription Skeletal Muscle Male skeletal muscle
4 chr12:10222000-10234800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
5 chr12:10222400-10227600 Weak transcription Adipose Nuclei Adipose
6 chr12:10222800-10248400 Weak transcription Psoas Muscle Psoas
7 chr12:10223000-10232600 Weak transcription Monocytes-CD14+_RO01746 blood
8 chr12:10223400-10226000 Weak transcription Right Ventricle heart
9 chr12:10223600-10232600 Weak transcription Primary monocytes fromperipheralblood blood
10 chr12:10224000-10234800 Weak transcription Lung lung
11 chr12:10225200-10226000 Strong transcription HUVEC blood vessel
12 chr12:10225400-10226000 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
13 chr12:10225600-10226200 Enhancers Breast Myoepithelial Primary Cells Breast
14 chr12:10225600-10226200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
15 chr12:10225600-10226400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
16 chr12:10225600-10226400 Enhancers HMEC breast
17 chr12:10225800-10226400 Enhancers NHEK skin
18 chr12:10225800-10226600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin

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