Variant report

Variant	rs34805563
Chromosome Location	chr14:68366533-68366534
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs35080917	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35106153	1.00[AMR][1000 genomes]
rs35575056	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35577122	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35917338	1.00[AMR][1000 genomes]
rs57048278	1.00[AMR][1000 genomes]
rs58431859	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58724136	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59429458	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60273960	1.00[AMR][1000 genomes]
rs61011477	1.00[AMR][1000 genomes]
rs61214213	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61341378	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61584136	1.00[AMR][1000 genomes]
rs73276671	1.00[AMR][1000 genomes]
rs73276676	1.00[AMR][1000 genomes]
rs73276687	1.00[AMR][1000 genomes]
rs73278432	1.00[AMR][1000 genomes]
rs73278469	1.00[AMR][1000 genomes]
rs73280405	1.00[AMR][1000 genomes]
rs73280424	1.00[AMR][1000 genomes]
rs73280429	1.00[AMR][1000 genomes]
rs73280438	1.00[AMR][1000 genomes]
rs73280465	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73280477	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73280481	1.00[AMR][1000 genomes]
rs73280491	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73282413	1.00[AMR][1000 genomes]
rs73282473	1.00[AMR][1000 genomes]

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:68328000-68367800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr14:68334600-68367600	Weak transcription	Primary B cells from cord blood	blood
3	chr14:68351400-68367600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr14:68351400-68367800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr14:68351600-68367400	Weak transcription	Primary hematopoietic stem cells	blood
6	chr14:68352000-68367600	Weak transcription	Primary T cells from cord blood	blood
7	chr14:68364200-68374000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
8	chr14:68364400-68368400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
9	chr14:68365800-68374800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr14:68366400-68367000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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