Variant report

Variant	rs11929956
Chromosome Location	chr4:128097223-128097224
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	chr4:128093003..128095000-chr4:128096462..128098842,3	K562	blood:

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10857123	0.90[ASN][1000 genomes]
rs11726994	0.88[ASN][1000 genomes]
rs11727022	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12639817	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13102188	0.80[ASN][1000 genomes]
rs13107241	0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs13111116	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13111239	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13111610	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13117384	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13118101	0.80[ASN][1000 genomes]
rs13122080	0.81[ASN][1000 genomes]
rs13123189	0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs13127462	0.90[ASN][1000 genomes]
rs13130460	0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13131457	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13135599	0.89[ASN][1000 genomes]
rs13135955	0.89[ASN][1000 genomes]
rs13148721	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1480905	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1480906	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17012108	0.90[ASN][1000 genomes]
rs35899860	0.92[ASN][1000 genomes]
rs4560424	0.83[ASN][1000 genomes]
rs4833369	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4834179	0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4834180	0.90[ASN][1000 genomes]
rs4834181	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs67169994	0.80[ASN][1000 genomes]
rs6817083	0.83[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6823821	0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7658955	0.90[ASN][1000 genomes]
rs7659106	0.90[ASN][1000 genomes]
rs7676467	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7682967	0.88[ASN][1000 genomes]
rs7683191	0.90[ASN][1000 genomes]
rs7683469	0.90[ASN][1000 genomes]
rs899933	0.94[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	nsv879914	chr4:128005362-128123638	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr4:128096200-128099600	Weak transcription	Colon Smooth Muscle	Colon
2	chr4:128097200-128097600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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