Variant report

Variant	rs55687119
Chromosome Location	chr7:26572348-26572349
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:26570553..26573015-chr7:26573523..26576136,3	K562	blood:

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10240247	1.00[ASN][1000 genomes]
rs10253181	1.00[ASN][1000 genomes]
rs12154305	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs34349657	0.89[ASN][1000 genomes]
rs55639061	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs55644320	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55668747	1.00[AMR][1000 genomes]
rs55715725	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs55779830	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs55871610	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs55992393	1.00[AMR][1000 genomes]
rs56099614	1.00[AMR][1000 genomes]
rs56157887	1.00[ASN][1000 genomes]
rs56158033	1.00[AMR][1000 genomes]
rs56171200	1.00[AMR][1000 genomes]
rs56325361	1.00[ASN][1000 genomes]
rs56408177	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6953881	1.00[ASN][1000 genomes]
rs6970244	1.00[ASN][1000 genomes]
rs6974982	1.00[ASN][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	nsv1029596	chr7:26302739-26737913	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
2	nsv538804	chr7:26302739-26737913	Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
3	nsv1025538	chr7:26482342-27376045	Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	213 gene(s)	inside rSNPs	diseases
4	nsv538805	chr7:26482342-27376045	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Strong transcription Flanking Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	213 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:26570800-26574400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr7:26571000-26578000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr7:26571200-26574200	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr7:26572200-26572400	Flanking Active TSS	Fetal Kidney	kidney
5	chr7:26572200-26572600	Enhancers	Primary hematopoietic stem cells	blood

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