Variant report

Variant rs17377380
Chromosome Location chr1:85250489-85250490
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 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 chr1:85246400-85250800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
4 chr1:85246400-85250800 Weak transcription NHEK skin
5 chr1:85246600-85250600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr1:85246600-85250600 Weak transcription HMEC breast
7 chr1:85248000-85251200 Weak transcription Fetal Heart heart
8 chr1:85248200-85250600 Weak transcription Brain Cingulate Gyrus brain
9 chr1:85248400-85250800 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
10 chr1:85248400-85250800 Weak transcription Brain Hippocampus Middle brain
11 chr1:85250200-85251800 Enhancers Stomach Smooth Muscle stomach
12 chr1:85250400-85252000 Enhancers Breast Myoepithelial Primary Cells Breast
13 chr1:85250400-85252000 Enhancers Rectal Smooth Muscle rectum

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