Variant report

Variant	rs6667843
Chromosome Location	chr1:151709200-151709201
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:151700800-151709800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr1:151702200-151709800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr1:151702600-151709600	Weak transcription	Right Atrium	heart
4	chr1:151702800-151712200	Weak transcription	Stomach Mucosa	stomach
5	chr1:151707600-151709800	Weak transcription	Liver	Liver
6	chr1:151707800-151709400	Weak transcription	Fetal Intestine Small	intestine
7	chr1:151707800-151710200	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr1:151707800-151712200	Weak transcription	Pancreas	Pancrea
9	chr1:151708000-151709400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr1:151708000-151709400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr1:151708000-151711800	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr1:151708400-151712200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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

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