Variant report

Variant	rs17011200
Chromosome Location	chr1:222191505-222191506
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs1078502	0.84[ASN][1000 genomes]
rs11118926	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12024555	0.81[EUR][1000 genomes]
rs12025565	0.84[EUR][1000 genomes]
rs12029332	0.86[EUR][1000 genomes]
rs12032653	0.86[EUR][1000 genomes]
rs12032715	0.80[EUR][1000 genomes]
rs12033415	0.92[EUR][1000 genomes]
rs12121134	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12125368	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12125383	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12129860	0.86[EUR][1000 genomes]
rs12135286	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12140604	0.92[EUR][1000 genomes]
rs12731064	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12739936	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1339871	0.92[ASN][1000 genomes]
rs17011182	0.92[EUR][1000 genomes]
rs17011186	0.92[ASN][1000 genomes]
rs17011190	0.92[ASN][1000 genomes]
rs17011199	0.92[ASN][1000 genomes]
rs17011202	0.92[ASN][1000 genomes]
rs17011219	0.88[ASN][1000 genomes]
rs17011229	0.88[ASN][1000 genomes]
rs17011236	0.88[ASN][1000 genomes]
rs17442058	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs17442323	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17495159	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2790759	0.92[ASN][1000 genomes]
rs35212520	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35718308	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs35805428	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56170536	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs56328548	0.92[ASN][1000 genomes]
rs56937190	0.86[ASN][1000 genomes]
rs57708351	0.86[ASN][1000 genomes]
rs58434051	0.80[ASN][1000 genomes]
rs58894876	0.92[ASN][1000 genomes]
rs59437737	0.86[ASN][1000 genomes]
rs66732677	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6687758	0.92[EUR][1000 genomes]
rs6691195	0.92[EUR][1000 genomes]
rs6695584	0.92[EUR][1000 genomes]
rs74147368	0.88[ASN][1000 genomes]
rs869254	0.84[ASN][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	nsv1014333	chr1:222131785-222245578	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs17011200	RP11-815M8.1	cis	lung	GTEx
rs17011200	RP11-400N13.2	cis	lung	GTEx

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:222190600-222191600	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr1:222190800-222194200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr1:222191000-222191800	Weak transcription	Skeletal Muscle Female	skeletal muscle
4	chr1:222191000-222192600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr1:222191400-222191800	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr1:222191400-222192000	Enhancers	ES-I3 Cell Line	embryonic stem cell

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