Variant report

Variant	rs72829630
Chromosome Location	chr6:15969209-15969210
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	chr6:15966000-15971200	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr6:15968400-15970800	Enhancers	Placenta	Placenta
3	chr6:15968400-15971000	Enhancers	HMEC	breast
4	chr6:15968600-15970600	Enhancers	NHEK	skin
5	chr6:15968600-15971000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr6:15968600-15971000	Enhancers	K562	blood
7	chr6:15969000-15970200	Enhancers	Placenta Amnion	Placenta Amnion
8	chr6:15969000-15970600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr6:15969000-15970600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr6:15969200-15969800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr6:15969200-15969800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr6:15969200-15970000	Enhancers	HSMMtube	muscle

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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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