Variant report

Variant	rs13361219
Chromosome Location	chr5:61600714-61600715
allele	A/C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:61593661..61595529-chr5:61600373..61601956,2	K562	blood:

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10051719	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10062387	0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10067200	0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10071537	0.81[ASN][1000 genomes]
rs10074813	0.85[AMR][1000 genomes]
rs10074863	0.88[AMR][1000 genomes]
rs10075026	0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10471278	0.81[AFR][1000 genomes];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10471544	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12655269	0.86[AFR][1000 genomes];0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12659793	0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12659814	0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13155700	0.83[ASN][1000 genomes]
rs13361143	0.83[ASN][1000 genomes]
rs152186	0.84[ASN][1000 genomes]
rs152204	0.80[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs152205	0.84[ASN][1000 genomes]
rs152210	0.84[ASN][1000 genomes]
rs16890622	0.82[ASN][1000 genomes]
rs1862527	0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1995782	0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs247225	0.92[AFR][1000 genomes];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs247227	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs247241	0.81[ASN][1000 genomes]
rs247242	0.84[ASN][1000 genomes]
rs247243	0.84[ASN][1000 genomes]
rs247250	0.84[ASN][1000 genomes]
rs247251	0.83[ASN][1000 genomes]
rs247254	0.94[AFR][1000 genomes];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs247259	0.85[ASN][1000 genomes]
rs247262	0.84[ASN][1000 genomes]
rs247264	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs247266	0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs27089	0.82[ASN][1000 genomes]
rs28589513	0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs35348760	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3822485	0.83[ASN][1000 genomes]
rs3846467	0.87[AFR][1000 genomes];0.92[AMR][1000 genomes];0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4145851	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4441833	0.83[ASN][1000 genomes]
rs4700006	0.83[ASN][1000 genomes]
rs56049450	0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs56317447	0.86[AFR][1000 genomes];0.91[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs67150497	0.83[ASN][1000 genomes]
rs9968583	0.83[ASN][1000 genomes]
rs9968586	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1024090	chr5:61258759-61921150	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	esv2757996	chr5:61403138-61687817	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	esv2759345	chr5:61403138-61748912	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
4	nsv830318	chr5:61415713-61623320	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv1020255	chr5:61451792-62031365	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
6	nsv1027539	chr5:61457762-62000008	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
7	esv2755585	chr5:61535831-61618595	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
8	nsv881726	chr5:61556730-61676911	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
9	nsv881727	chr5:61578041-61700970	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	23 gene(s)	inside rSNPs	diseases
10	nsv10703	chr5:61596178-61601493	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:61596200-61600800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr5:61596200-61600800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr5:61596200-61600800	Weak transcription	Dnd41	blood
4	chr5:61596200-61601000	Weak transcription	Placenta	Placenta
5	chr5:61596200-61601000	Weak transcription	Thymus	Thymus
6	chr5:61596200-61601200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr5:61596800-61600800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
8	chr5:61596800-61600800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
9	chr5:61596800-61600800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
10	chr5:61596800-61600800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
11	chr5:61596800-61601000	Weak transcription	Primary T cells from cord blood	blood
12	chr5:61596800-61601000	Weak transcription	Fetal Thymus	thymus
13	chr5:61599400-61601000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
14	chr5:61600200-61601000	Weak transcription	GM12878-XiMat	blood
15	chr5:61600400-61601000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
16	chr5:61600400-61601000	Enhancers	Primary T helper cells fromperipheralblood	blood
17	chr5:61600400-61601000	Enhancers	Primary T killer memory cells from peripheral blood	blood
18	chr5:61600400-61601200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
19	chr5:61600600-61601000	Enhancers	Primary T helper cells PMA-I stimulated	--
20	chr5:61600600-61601200	Enhancers	Primary T cells fromperipheralblood	blood

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