Variant report

Variant	rs7658908
Chromosome Location	chr4:21100703-21100704
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:21099804..21101899-chr4:21102257..21105155,2	K562	blood:

Extended variants
information (count: 52 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10022535	0.85[ASN][1000 genomes]
rs10433822	1.00[ASN][1000 genomes]
rs10938831	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11735843	1.00[ASN][1000 genomes]
rs11735844	1.00[ASN][1000 genomes]
rs11736507	1.00[ASN][1000 genomes]
rs11736572	1.00[ASN][1000 genomes]
rs11935122	0.83[ASN][1000 genomes]
rs11944165	0.83[ASN][1000 genomes]
rs12639638	1.00[ASN][1000 genomes]
rs12640310	1.00[ASN][1000 genomes]
rs12642886	1.00[ASN][1000 genomes]
rs12644882	1.00[ASN][1000 genomes]
rs12644941	0.99[ASN][1000 genomes]
rs12646316	1.00[ASN][1000 genomes]
rs12647437	1.00[ASN][1000 genomes]
rs1368646	1.00[ASN][1000 genomes]
rs1368648	1.00[ASN][1000 genomes]
rs17574283	0.85[ASN][1000 genomes]
rs17637027	0.98[ASN][1000 genomes]
rs2043388	0.86[EUR][1000 genomes]
rs2163931	0.98[ASN][1000 genomes]
rs4572877	1.00[ASN][1000 genomes]
rs4590029	1.00[ASN][1000 genomes]
rs4599408	0.85[ASN][1000 genomes]
rs55737345	0.80[ASN][1000 genomes]
rs55885656	0.83[ASN][1000 genomes]
rs55957496	0.98[ASN][1000 genomes]
rs56025335	0.80[ASN][1000 genomes]
rs56139613	0.81[ASN][1000 genomes]
rs56412118	0.85[ASN][1000 genomes]
rs58548088	1.00[ASN][1000 genomes]
rs59223154	1.00[ASN][1000 genomes]
rs59416831	1.00[ASN][1000 genomes]
rs60444813	1.00[ASN][1000 genomes]
rs61644618	1.00[ASN][1000 genomes]
rs6810466	0.83[ASN][1000 genomes]
rs6810897	0.83[ASN][1000 genomes]
rs6815915	0.83[ASN][1000 genomes]
rs6817687	0.85[ASN][1000 genomes]
rs6832569	0.83[ASN][1000 genomes]
rs6832607	0.83[ASN][1000 genomes]
rs6840528	0.85[ASN][1000 genomes]
rs6845231	0.87[EUR][1000 genomes]
rs73802481	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1014941	chr4:20611726-21345226	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv537053	chr4:20611726-21345226	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv1013365	chr4:20834054-21609078	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
4	nsv829878	chr4:20966047-21138626	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv878745	chr4:21054348-21155716	Enhancers Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv878746	chr4:21054348-21169062	Enhancers Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv878747	chr4:21057794-21169062	Enhancers Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:21099200-21104400	Weak transcription	HUVEC	blood vessel

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