Variant report

Variant rs145133195
Chromosome Location chr1:93274252-93274253
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:93271000-93276000 Weak transcription Placenta Amnion Placenta Amnion
2 chr1:93271800-93276800 Weak transcription K562 blood
3 chr1:93272600-93276000 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
4 chr1:93273000-93275000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr1:93273000-93275200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr1:93273400-93275000 Enhancers HMEC breast
7 chr1:93273400-93275000 Enhancers NHEK skin
8 chr1:93273600-93274400 Enhancers Osteobl bone
9 chr1:93273600-93274600 Enhancers Muscle Satellite Cultured Cells --
10 chr1:93273600-93275000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr1:93273600-93275000 Enhancers Placenta Placenta
12 chr1:93273600-93275000 Enhancers Hela-S3 cervix
13 chr1:93274000-93274400 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
14 chr1:93274000-93275800 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
15 chr1:93274200-93274600 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived

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