Variant report

Variant rs61770439
Chromosome Location chr1:85249858-85249859
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:85241000-85263600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr1:85246000-85250600 Weak transcription Colon Smooth Muscle Colon
3 chr1:85246200-85250200 Weak transcription Stomach Smooth Muscle stomach
4 chr1:85246400-85250800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
5 chr1:85246400-85250800 Weak transcription NHEK skin
6 chr1:85246600-85250400 Weak transcription Breast Myoepithelial Primary Cells Breast
7 chr1:85246600-85250600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr1:85246600-85250600 Weak transcription HMEC breast
9 chr1:85248000-85251200 Weak transcription Fetal Heart heart
10 chr1:85248200-85250600 Weak transcription Brain Cingulate Gyrus brain
11 chr1:85248400-85250800 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
12 chr1:85248400-85250800 Weak transcription Brain Hippocampus Middle brain

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