Variant report

Variant	rs10221846
Chromosome Location	chr2:188176291-188176292
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10174402	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10174460	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10208253	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10931287	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13388347	1.00[AMR][1000 genomes]
rs13391909	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13392210	0.85[AFR][1000 genomes]
rs13399503	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13401664	1.00[AMR][1000 genomes]
rs13401762	1.00[AMR][1000 genomes]
rs13405653	0.85[AFR][1000 genomes]
rs13409677	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13414158	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13427655	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13430432	0.85[AFR][1000 genomes]
rs13432027	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28363963	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28458997	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28585422	1.00[AMR][1000 genomes]
rs6434212	1.00[AMR][1000 genomes]
rs6715996	0.85[AFR][1000 genomes]
rs6721057	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6747392	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6753145	0.85[AFR][1000 genomes]
rs7578599	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7583999	1.00[AMR][1000 genomes]
rs7592458	0.85[AFR][1000 genomes]
rs7599181	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949700	chr2:187713412-188361211	Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv1003061	chr2:187950057-188282330	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv1000617	chr2:187950057-188290511	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv533935	chr2:188089148-188284766	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:188175800-188180800	Weak transcription	HUVEC	blood vessel

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