Variant report

Variant	rs17034187
Chromosome Location	chr12:103988385-103988386
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10861044	1.00[ASN][1000 genomes]
rs10861045	1.00[ASN][1000 genomes]
rs10861046	1.00[ASN][1000 genomes]
rs10861047	1.00[ASN][1000 genomes]
rs10861048	0.99[ASN][1000 genomes]
rs10861049	0.97[ASN][1000 genomes]
rs10861050	0.81[ASN][1000 genomes]
rs10861051	0.99[ASN][1000 genomes]
rs11111672	0.99[ASN][1000 genomes]
rs11111673	0.99[ASN][1000 genomes]
rs11111674	0.99[ASN][1000 genomes]
rs12367313	0.99[ASN][1000 genomes]
rs12832814	1.00[EUR][1000 genomes]
rs1305368	0.98[ASN][1000 genomes]
rs1593806	1.00[ASN][1000 genomes]
rs1593810	1.00[EUR][1000 genomes]
rs1593811	1.00[EUR][1000 genomes]
rs1593812	1.00[EUR][1000 genomes]
rs1593813	1.00[EUR][1000 genomes]
rs1610171	1.00[ASN][1000 genomes]
rs1610202	0.96[ASN][1000 genomes]
rs17034119	1.00[EUR][1000 genomes]
rs17034127	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17034172	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2086244	0.99[ASN][1000 genomes]
rs2086245	0.99[ASN][1000 genomes]
rs2086246	0.99[ASN][1000 genomes]
rs2100980	0.99[ASN][1000 genomes]
rs2100981	0.99[ASN][1000 genomes]
rs35929067	0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4015364	0.99[ASN][1000 genomes]
rs56402195	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56916543	0.99[ASN][1000 genomes]
rs58261212	0.81[ASN][1000 genomes]
rs6539085	0.97[ASN][1000 genomes]
rs7134377	1.00[ASN][1000 genomes]
rs7953892	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7958707	0.81[ASN][1000 genomes]
rs7958798	0.81[ASN][1000 genomes]
rs7958925	0.96[ASN][1000 genomes]
rs7966214	0.99[ASN][1000 genomes]
rs7969320	0.99[ASN][1000 genomes]
rs7979192	0.99[ASN][1000 genomes]
rs7979345	0.99[ASN][1000 genomes]
rs7979507	0.99[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	esv3391153	chr12:103983229-103989747	Enhancers Weak transcription	TF binding region Chromatin interactive region	1 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	chr12:103988200-103988400	Enhancers	Spleen	Spleen

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