Variant report

Variant	rs16903626
Chromosome Location	chr8:129802456-129802457
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs16903630	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs16903929	1.00[EUR][1000 genomes]
rs2056312	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2116456	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7009989	1.00[CEU][hapmap];0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:129784000-129809800	Weak transcription	Dnd41	blood
2	chr8:129801000-129805200	Weak transcription	HUVEC	blood vessel
3	chr8:129801000-129806000	Weak transcription	HSMM	muscle
4	chr8:129801000-129806600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr8:129801200-129806000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr8:129801200-129806600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr8:129801400-129806200	Weak transcription	NHDF-Ad	bronchial
8	chr8:129801400-129806600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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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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