Variant report

Variant	rs57145061
Chromosome Location	chr8:49378948-49378949
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:49378400-49380600	Enhancers	K562	blood
2	chr8:49378600-49380600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr8:49378600-49381400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr8:49378800-49379000	Enhancers	Fetal Intestine Large	intestine
5	chr8:49378800-49379000	Enhancers	Fetal Thymus	thymus
6	chr8:49378800-49379400	Enhancers	Placenta Amnion	Placenta Amnion
7	chr8:49378800-49380800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr8:49378800-49383000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

what's new

Quick links