Variant report

Variant rs6678912
Chromosome Location chr1:186471301-186471302
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:186459400-186471800 Weak transcription Brain Angular Gyrus brain
2 chr1:186467000-186471400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
3 chr1:186467200-186474400 Enhancers NHDF-Ad bronchial
4 chr1:186468800-186472200 Weak transcription NH-A brain
5 chr1:186469200-186472200 Weak transcription Muscle Satellite Cultured Cells --
6 chr1:186469200-186472200 Enhancers A549 lung
7 chr1:186469400-186472400 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
8 chr1:186469800-186472600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
9 chr1:186469800-186473200 Weak transcription Aorta Aorta
10 chr1:186470200-186471400 Enhancers HUES48 Cell Line embryonic stem cell
11 chr1:186470200-186493200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr1:186470400-186473000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr1:186470800-186473400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
14 chr1:186470800-186473600 Enhancers Osteobl bone
15 chr1:186471000-186471400 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
16 chr1:186471200-186471400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin

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