Variant report

Variant	rs16915436
Chromosome Location	chr11:26318959-26318960
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10501044	0.93[AFR][1000 genomes]
rs10501047	0.82[AFR][1000 genomes]
rs10834952	0.82[AFR][1000 genomes]
rs10834962	0.82[AFR][1000 genomes]
rs11029465	0.90[AFR][1000 genomes]
rs11029467	0.90[AFR][1000 genomes]
rs11029468	0.90[AFR][1000 genomes]
rs11029469	0.90[AFR][1000 genomes]
rs11029470	0.86[AFR][1000 genomes]
rs11029473	0.80[AFR][1000 genomes]
rs11029474	0.90[AFR][1000 genomes]
rs11029475	0.90[AFR][1000 genomes]
rs11029483	0.81[YRI][hapmap]
rs11820185	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11824243	0.90[AFR][1000 genomes]
rs11824253	0.80[AFR][1000 genomes]
rs11824306	0.87[AFR][1000 genomes]
rs11824431	0.89[AFR][1000 genomes]
rs11826153	0.85[YRI][hapmap];0.82[AFR][1000 genomes]
rs11826224	0.82[AFR][1000 genomes]
rs11826876	0.89[AFR][1000 genomes]
rs11827865	0.85[YRI][hapmap];0.82[AFR][1000 genomes]
rs12049824	0.82[AFR][1000 genomes]
rs12221994	0.82[AFR][1000 genomes]
rs12223352	0.93[AFR][1000 genomes]
rs12223726	0.82[AFR][1000 genomes]
rs16915437	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16915466	0.82[AFR][1000 genomes]
rs1960495	0.82[AFR][1000 genomes]
rs34019155	0.87[AFR][1000 genomes]
rs34362229	0.90[AFR][1000 genomes]
rs34411356	0.87[AFR][1000 genomes]
rs35215165	0.90[AFR][1000 genomes]
rs35624765	0.87[AFR][1000 genomes]
rs60193609	0.90[AFR][1000 genomes]
rs60811682	0.82[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3425701	chr11:26310425-26330495	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:26318600-26319600	Enhancers	Fetal Lung	lung
2	chr11:26318800-26319400	Enhancers	Fetal Kidney	kidney

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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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