Variant report

Variant	rs614837
Chromosome Location	chr6:24945894-24945895
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs1739317	1.00[ASN][1000 genomes]
rs421817	0.84[YRI][hapmap]
rs495157	0.84[YRI][hapmap]
rs586557	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs599699	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs604926	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs604945	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs614900	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs628794	0.84[YRI][hapmap]
rs644722	0.84[YRI][hapmap]
rs644748	0.84[YRI][hapmap]
rs685008	0.86[YRI][hapmap]
rs73382348	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73382352	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7738180	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7757708	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7775482	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7775697	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1022966	chr6:24763776-25154212	Flanking Active TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	nsv538160	chr6:24763776-25154212	Active TSS Strong transcription Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
3	nsv1019504	chr6:24869174-24994758	Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv883482	chr6:24926730-25035920	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
5	nsv1023989	chr6:24930362-25285679	Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
6	nsv1030634	chr6:24938277-25040161	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:24941400-24946200	Weak transcription	Fetal Thymus	thymus
2	chr6:24942400-24948000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr6:24943800-24946000	ZNF genes & repeats	Primary B cells from peripheral blood	blood
4	chr6:24943800-24946000	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
5	chr6:24943800-24948000	ZNF genes & repeats	Dnd41	blood
6	chr6:24944000-24946000	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 1	blood
7	chr6:24944000-24946000	ZNF genes & repeats	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr6:24944800-24949200	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr6:24945000-24946800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
10	chr6:24945200-24946200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr6:24945200-24946400	Weak transcription	Primary hematopoietic stem cells	blood
12	chr6:24945600-24946600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
13	chr6:24945800-24946400	Weak transcription	Primary T cells fromperipheralblood	blood
14	chr6:24945800-24946600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
15	chr6:24945800-24946600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
16	chr6:24945800-24946600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
17	chr6:24945800-24946600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr6:24945800-24946800	Weak transcription	Primary T killer memory cells from peripheral blood	blood

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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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