Variant report

Variant	rs34732137
Chromosome Location	chr3:60022998-60022999
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs11925432	0.89[ASN][1000 genomes]
rs13060068	1.00[ASN][1000 genomes]
rs13061158	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs17061932	1.00[ASN][1000 genomes]
rs17061972	0.89[ASN][1000 genomes]
rs17256807	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs17257269	0.97[AFR][1000 genomes];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs212010	0.89[ASN][1000 genomes]
rs34267930	0.89[ASN][1000 genomes]
rs35066861	0.86[EUR][1000 genomes]
rs35226385	0.85[EUR][1000 genomes]
rs35688021	0.80[EUR][1000 genomes]
rs3845974	0.89[ASN][1000 genomes]
rs3856662	0.85[EUR][1000 genomes]
rs4024131	1.00[ASN][1000 genomes]
rs57439204	0.89[ASN][1000 genomes]
rs67136973	0.89[ASN][1000 genomes]
rs6779716	0.84[EUR][1000 genomes]
rs6779755	0.85[EUR][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	nsv428085	chr3:59782509-60070116	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1014983	chr3:59884024-60558331	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv590387	chr3:59890976-60481459	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv834707	chr3:60005679-60184046	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:60020200-60030000	Weak transcription	Primary T cells from cord blood	blood
2	chr3:60021000-60024800	Weak transcription	Primary T helper cells fromperipheralblood	blood
3	chr3:60021000-60031600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
4	chr3:60021800-60026400	Weak transcription	Fetal Thymus	thymus
5	chr3:60022200-60030000	Weak transcription	Thymus	Thymus
6	chr3:60022400-60023000	Genic enhancers	Dnd41	blood
7	chr3:60022600-60026200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
8	chr3:60022800-60026200	Weak transcription	Primary T helper cells PMA-I stimulated	--

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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