Variant report

Variant rs227196
Chromosome Location chr1:210166412-210166413
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:210159400-210166600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
2 chr1:210159600-210168200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
3 chr1:210162800-210189200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr1:210166200-210166800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
5 chr1:210166200-210166800 Enhancers Brain Substantia Nigra brain
6 chr1:210166200-210167000 Enhancers Brain Cingulate Gyrus brain
7 chr1:210166200-210167200 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
8 chr1:210166200-210167200 Genic enhancers Foreskin Melanocyte Primary Cells skin03 Skin
9 chr1:210166400-210166600 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
10 chr1:210166400-210166800 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
11 chr1:210166400-210166800 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
12 chr1:210166400-210167000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
13 chr1:210166400-210167000 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin01 Skin
14 chr1:210166400-210167000 Enhancers Brain Hippocampus Middle brain

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