Variant report

Variant rs7555819
Chromosome Location chr1:245950642-245950643
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:245932000-245966200 Weak transcription Primary T cells from cord blood blood
2 chr1:245935800-245952000 Weak transcription K562 blood
3 chr1:245943800-245951000 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
4 chr1:245946600-245951200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr1:245946800-245950800 Weak transcription Fetal Heart heart
6 chr1:245949200-245961400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
7 chr1:245949200-245999600 Weak transcription Gastric stomach
8 chr1:245949800-245955000 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
9 chr1:245950400-245952400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
10 chr1:245950600-245951200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr1:245950600-245951200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
12 chr1:245950600-245951200 Enhancers NHDF-Ad bronchial
13 chr1:245950600-245951200 Enhancers NHLF lung
14 chr1:245950600-245952200 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived

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