Variant report

Variant	rs57925841
Chromosome Location	chr4:90808191-90808192
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:90806651..90808607-chr4:90809105..90812073,2	K562	blood:

Extended variants
information (count: 62 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs10433954	0.89[ASN][1000 genomes]
rs10433955	0.89[ASN][1000 genomes]
rs10516850	0.87[ASN][1000 genomes]
rs10516851	0.87[ASN][1000 genomes]
rs10516852	0.87[ASN][1000 genomes]
rs11722543	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12640573	0.87[ASN][1000 genomes]
rs12640925	0.89[ASN][1000 genomes]
rs12640973	0.89[ASN][1000 genomes]
rs12641781	0.87[ASN][1000 genomes]
rs12643790	0.86[ASN][1000 genomes]
rs12643823	0.87[ASN][1000 genomes]
rs12644375	0.87[ASN][1000 genomes]
rs1372511	1.00[ASN][1000 genomes]
rs1372512	1.00[ASN][1000 genomes]
rs1442131	0.90[ASN][1000 genomes]
rs1442132	1.00[ASN][1000 genomes]
rs17016373	0.88[ASN][1000 genomes]
rs2241884	0.87[ASN][1000 genomes]
rs3775464	0.89[ASN][1000 genomes]
rs3775465	0.89[ASN][1000 genomes]
rs3775466	0.89[ASN][1000 genomes]
rs3775467	0.89[ASN][1000 genomes]
rs3775473	0.86[ASN][1000 genomes]
rs3775474	0.87[ASN][1000 genomes]
rs3775476	0.87[ASN][1000 genomes]
rs3775477	0.87[ASN][1000 genomes]
rs3775478	0.87[ASN][1000 genomes]
rs56146644	0.89[ASN][1000 genomes]
rs58514521	0.89[ASN][1000 genomes]
rs58930449	0.83[ASN][1000 genomes]
rs59559279	0.98[ASN][1000 genomes]
rs60341854	0.86[ASN][1000 genomes]
rs60847430	0.89[ASN][1000 genomes]
rs61160271	0.87[ASN][1000 genomes]
rs61611959	0.82[ASN][1000 genomes]
rs6532197	1.00[ASN][1000 genomes]
rs6532199	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6532200	0.92[ASN][1000 genomes]
rs6828095	1.00[ASN][1000 genomes]
rs6838943	0.90[ASN][1000 genomes]
rs6847403	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6848022	1.00[ASN][1000 genomes]
rs6857668	0.84[ASN][1000 genomes]
rs6858182	0.86[ASN][1000 genomes]
rs72657800	0.90[ASN][1000 genomes]
rs72657801	0.89[ASN][1000 genomes]
rs72657802	0.89[ASN][1000 genomes]
rs72659403	0.89[ASN][1000 genomes]
rs72659404	0.89[ASN][1000 genomes]
rs72659409	0.87[ASN][1000 genomes]
rs72659413	0.83[ASN][1000 genomes]
rs73831836	1.00[ASN][1000 genomes]
rs73831856	0.84[ASN][1000 genomes]
rs7657014	0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7666981	0.89[ASN][1000 genomes]
rs7673735	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2830400	chr4:90085456-90922432	Flanking Active TSS Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv1012406	chr4:90167781-91166787	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
3	nsv949454	chr4:90272120-91156917	Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
4	nsv997700	chr4:90791866-90920021	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv830005	chr4:90799398-90963420	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr4:90800200-90809200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr4:90807600-90808200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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