Variant report

Variant	rs61831997
Chromosome Location	chr1:193602366-193602367
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:193602279..193604026-chr1:193606853..193608371,2	K562	blood:
2	chr1:193596850..193598572-chr1:193600474..193603843,3	K562	blood:

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10489939	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17304406	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17304707	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17304721	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17304880	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17376294	0.91[ASN][1000 genomes]
rs17376406	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17376588	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17376643	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17376657	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17376699	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17376728	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17376854	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17376861	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2031832	0.88[ASN][1000 genomes]
rs2039761	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2039762	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2039763	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2039764	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2149178	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs41409146	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs41533746	0.83[AFR][1000 genomes];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs55874905	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs55950830	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs56003845	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs56106540	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs57049435	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs57730370	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs58874275	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs59209979	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs61242642	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs61831965	0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs61831966	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs61832001	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs61832029	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs61832030	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs61833662	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs61833663	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs61833664	0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs61833665	0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs61833666	0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs61833667	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs61833671	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6659749	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6671716	0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72728933	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72728954	1.00[AFR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72728968	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs72744026	0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9787078	0.83[EUR][1000 genomes];0.88[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	nsv1008266	chr1:193550185-194481053	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:193586200-193603200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr1:193596800-193603800	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr1:193599400-193603400	Weak transcription	Primary monocytes fromperipheralblood	blood
4	chr1:193600200-193603400	Weak transcription	Primary T cells from cord blood	blood
5	chr1:193601800-193602400	Enhancers	Colon Smooth Muscle	Colon
6	chr1:193602000-193602600	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr1:193602200-193603600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--

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