Variant report

Variant rs2677113
Chromosome Location chr1:215838999-215839000
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:215837000-215841200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
2 chr1:215837000-215843600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr1:215837200-215840200 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
4 chr1:215837400-215842600 Weak transcription H9 Cell Line embryonic stem cell
5 chr1:215838000-215839000 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
6 chr1:215838400-215839000 Enhancers H1 Cell Line embryonic stem cell
7 chr1:215838400-215839000 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
8 chr1:215838400-215839400 Enhancers NH-A brain
9 chr1:215838400-215839800 Enhancers Osteobl bone
10 chr1:215838400-215840000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr1:215838600-215839000 Enhancers iPS-18 Cell Line embryonic stem cell
12 chr1:215838600-215839200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr1:215838600-215839800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
14 chr1:215838800-215839000 Enhancers HUES6 Cell Line embryonic stem cell
15 chr1:215838800-215839400 Enhancers iPS-20b Cell Line embryonic stem cell
16 chr1:215838800-215839400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow

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