Variant report

Variant rs6976399
Chromosome Location chr7:106654877-106654878
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:106654400-106655000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
2 chr7:106654600-106655000 Enhancers Adipose Nuclei Adipose
3 chr7:106654600-106655400 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Male --
4 chr7:106654600-106655400 Enhancers Psoas Muscle Psoas
5 chr7:106654600-106655600 Enhancers Fetal Brain Male brain
6 chr7:106654800-106655000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
7 chr7:106654800-106655200 Enhancers Colon Smooth Muscle Colon
8 chr7:106654800-106655200 Enhancers HUVEC blood vessel
9 chr7:106654800-106655400 Enhancers ES-I3 Cell Line embryonic stem cell
10 chr7:106654800-106655400 Enhancers iPS-18 Cell Line embryonic stem cell
11 chr7:106654800-106655400 Active TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
12 chr7:106654800-106655400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
13 chr7:106654800-106655400 Flanking Active TSS Fetal Heart heart
14 chr7:106654800-106655600 Enhancers Fetal Stomach stomach
15 chr7:106654800-106655600 Flanking Active TSS K562 blood

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