Variant report

Variant rs2139835
Chromosome Location chr1:151710659-151710660
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 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 chr1:151709400-151710800 ZNF genes & repeats Fetal Intestine Small intestine
6 chr1:151710200-151712800 Enhancers Skeletal Muscle Female skeletal muscle
7 chr1:151710600-151711200 Weak transcription Fetal Intestine Large intestine
8 chr1:151710600-151713000 Enhancers Liver Liver

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