Variant report

Variant rs4845340
Chromosome Location chr1:151710400-151710401
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:151702800-151712200 Weak transcription Stomach Mucosa stomach
2 chr1:151707800-151712200 Weak transcription Pancreas Pancrea
3 chr1:151708000-151711800 Weak transcription Placenta Amnion Placenta Amnion
4 chr1:151708400-151712200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr1:151709400-151710600 ZNF genes & repeats Foreskin Melanocyte Primary Cells skin01 Skin
6 chr1:151709400-151710800 ZNF genes & repeats Fetal Intestine Small intestine
7 chr1:151709800-151710400 ZNF genes & repeats H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
8 chr1:151709800-151710400 ZNF genes & repeats H1 Derived Mesenchymal Stem Cells ES cell derived
9 chr1:151709800-151710400 ZNF genes & repeats Liver Liver
10 chr1:151710200-151710400 ZNF genes & repeats Aorta Aorta
11 chr1:151710200-151712800 Enhancers Skeletal Muscle Female skeletal muscle
12 chr1:151710400-151710600 Weak transcription Liver Liver

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