Variant report

Variant	rs8065626
Chromosome Location	chr17:33813292-33813293
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs12451141	0.82[CEU][hapmap];0.87[EUR][1000 genomes]
rs12451679	0.85[CEU][hapmap];0.81[CHD][hapmap];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12453650	0.91[EUR][1000 genomes]
rs16970988	0.81[JPT][hapmap];0.91[EUR][1000 genomes]
rs16971025	0.85[CEU][hapmap];0.90[CHB][hapmap];0.81[CHD][hapmap];0.87[JPT][hapmap];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs62078141	0.91[EUR][1000 genomes]
rs62078142	0.91[EUR][1000 genomes]
rs62078145	0.91[EUR][1000 genomes]
rs62078151	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62078154	0.89[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	nsv1055936	chr17:33327166-33884184	Strong transcription Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	112 gene(s)	inside rSNPs	diseases
2	nsv543317	chr17:33327166-33884184	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	112 gene(s)	inside rSNPs	diseases
3	nsv534371	chr17:33456878-34094068	Strong transcription Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	137 gene(s)	inside rSNPs	diseases
4	nsv574741	chr17:33552275-33827134	Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	72 gene(s)	inside rSNPs	diseases
5	nsv1056116	chr17:33691457-33815452	Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs8065626	SLFN11	cis	lymphoblastoid	seeQTL

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:33809800-33813800	Weak transcription	Spleen	Spleen
2	chr17:33810400-33813800	Weak transcription	GM12878-XiMat	blood
3	chr17:33811600-33813800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr17:33811600-33814000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr17:33812400-33813800	Enhancers	Primary T killer memory cells from peripheral blood	blood
6	chr17:33812600-33813600	Enhancers	Primary T helper cells fromperipheralblood	blood
7	chr17:33812600-33813800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
8	chr17:33812800-33813600	Genic enhancers	Primary T helper cells PMA-I stimulated	--
9	chr17:33812800-33813800	Genic enhancers	Primary T helper naive cells from peripheral blood	blood
10	chr17:33812800-33814000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
11	chr17:33812800-33814000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
12	chr17:33812800-33820400	Strong transcription	Dnd41	blood
13	chr17:33813000-33813400	ZNF genes & repeats	Primary T cells from cord blood	blood
14	chr17:33813000-33813800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
15	chr17:33813200-33813800	Genic enhancers	Primary T cells fromperipheralblood	blood
16	chr17:33813200-33813800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
17	chr17:33813200-33813800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
18	chr17:33813200-33813800	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
19	chr17:33813200-33814000	Bivalent Enhancer	Fetal Thymus	thymus

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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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