Variant report

Variant	rs17516329
Chromosome Location	chr1:92319781-92319782
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10157853	0.82[YRI][hapmap]
rs10493857	0.95[CEU][hapmap];0.87[CHB][hapmap];0.83[CHD][hapmap];0.97[GIH][hapmap];0.95[MEX][hapmap];0.92[MKK][hapmap];0.94[TSI][hapmap];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10875030	0.95[CEU][hapmap];0.87[TSI][hapmap]
rs11165595	0.87[CEU][hapmap];0.83[CHB][hapmap];0.86[CHD][hapmap]
rs11165637	0.81[AMR][1000 genomes]
rs11165679	0.95[CEU][hapmap];0.87[CHB][hapmap];0.83[CHD][hapmap];0.97[GIH][hapmap];0.95[MEX][hapmap];0.88[MKK][hapmap];0.97[TSI][hapmap];0.82[YRI][hapmap];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11165681	1.00[YRI][hapmap];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11580031	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11580045	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11590254	1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];0.83[MKK][hapmap];1.00[TSI][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1192524	0.95[CEU][hapmap];0.97[GIH][hapmap];0.95[MEX][hapmap];0.88[MKK][hapmap];0.94[TSI][hapmap];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12026798	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12043241	0.84[CEU][hapmap]
rs12127774	0.95[CEU][hapmap]
rs12569180	0.95[CEU][hapmap];0.87[CHB][hapmap];0.83[CHD][hapmap];0.97[GIH][hapmap];0.95[MEX][hapmap];0.92[MKK][hapmap];0.97[TSI][hapmap];0.82[YRI][hapmap];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12725483	0.82[YRI][hapmap]
rs12726500	0.86[CEU][hapmap];0.83[CHB][hapmap];0.86[CHD][hapmap]
rs17576372	0.88[MKK][hapmap]
rs17881430	0.91[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.88[MKK][hapmap];1.00[TSI][hapmap];0.82[YRI][hapmap];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2450924	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2489188	0.87[CHB][hapmap];0.83[CHD][hapmap];0.82[MEX][hapmap];0.85[EUR][1000 genomes]
rs28403919	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs284147	0.91[CEU][hapmap];0.83[CHB][hapmap]
rs284149	0.87[CEU][hapmap];0.83[CHB][hapmap]
rs284153	0.87[CEU][hapmap];0.83[CHB][hapmap]
rs284159	0.86[CEU][hapmap];0.83[CHB][hapmap]
rs416624	0.87[CEU][hapmap];0.83[CHB][hapmap]
rs61779066	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6656018	0.95[CEU][hapmap];0.87[TSI][hapmap];0.84[EUR][1000 genomes]
rs7555476	0.87[CEU][hapmap];0.83[CHB][hapmap];0.86[CHD][hapmap]
rs7555548	0.87[CEU][hapmap];0.83[CHB][hapmap];0.85[CHD][hapmap]
rs9661103	0.95[CEU][hapmap];0.92[TSI][hapmap];0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:24 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1012864	chr1:92067100-92827761	Flanking Active TSS Strong transcription Enhancers Active TSS Weak transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
2	nsv535029	chr1:92067100-92827761	Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
3	nsv530438	chr1:92091957-92827760	Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
4	nsv1010179	chr1:92140209-92655952	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
5	nsv535030	chr1:92140209-92655952	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
6	nsv1005917	chr1:92189945-92378683	Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv949449	chr1:92211020-92585831	Strong transcription Enhancers Genic enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
8	nsv524845	chr1:92215725-92598705	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
9	nsv462517	chr1:92215725-92598705	Weak transcription Bivalent Enhancer Enhancers Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
10	nsv546810	chr1:92215725-92598705	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
11	nsv1006318	chr1:92216408-92608324	Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
12	nsv432498	chr1:92218245-92618323	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
13	nsv1004570	chr1:92220544-92622129	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
14	nsv1007661	chr1:92220544-92655952	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
15	nsv1014837	chr1:92233905-92618839	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
16	nsv535031	chr1:92233905-92618839	Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
17	nsv1012134	chr1:92235485-92598800	Weak transcription Genic enhancers Flanking Active TSS Active TSS Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
18	nsv546818	chr1:92236048-92579206	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
19	nsv546819	chr1:92256626-92558583	Strong transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
20	nsv546820	chr1:92273644-92558583	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
21	nsv530046	chr1:92277460-92799794	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
22	nsv1007270	chr1:92289298-92598800	Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
23	nsv1002730	chr1:92302541-92565229	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
24	nsv830581	chr1:92317207-92511175	Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs17516329	GBP7	cis	parietal	SCAN
rs17516329	GFI1	cis	parietal	SCAN

Chromatin state (count:57 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:92296400-92335800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr1:92300800-92329600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr1:92312000-92329800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
4	chr1:92312000-92337200	Weak transcription	Fetal Intestine Small	intestine
5	chr1:92312600-92322200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr1:92312800-92325600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr1:92313800-92328200	Weak transcription	Esophagus	oesophagus
8	chr1:92315000-92329800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
9	chr1:92315200-92330200	Weak transcription	Spleen	Spleen
10	chr1:92316800-92325000	Weak transcription	Primary T cells fromperipheralblood	blood
11	chr1:92317000-92330000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr1:92317200-92329000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr1:92317400-92320000	Strong transcription	Fetal Stomach	stomach
14	chr1:92317400-92329200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr1:92317400-92329800	Weak transcription	Fetal Kidney	kidney
16	chr1:92317400-92337200	Weak transcription	K562	blood
17	chr1:92317400-92338000	Weak transcription	Rectal Mucosa Donor 29	rectum
18	chr1:92317400-92344400	Weak transcription	Fetal Intestine Large	intestine
19	chr1:92317600-92320400	Weak transcription	Rectal Smooth Muscle	rectum
20	chr1:92317600-92320600	Weak transcription	Colon Smooth Muscle	Colon
21	chr1:92317600-92324600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr1:92317600-92325600	Weak transcription	Liver	Liver
23	chr1:92317600-92329200	Weak transcription	Osteobl	bone
24	chr1:92317600-92329600	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr1:92317600-92335800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
26	chr1:92317800-92320600	Weak transcription	Fetal Muscle Leg	muscle
27	chr1:92317800-92326000	Weak transcription	Fetal Muscle Trunk	muscle
28	chr1:92318000-92320000	Weak transcription	Stomach Smooth Muscle	stomach
29	chr1:92318000-92320200	Weak transcription	Skeletal Muscle Male	skeletal muscle
30	chr1:92318000-92320600	Weak transcription	Skeletal Muscle Female	skeletal muscle
31	chr1:92318000-92320800	Weak transcription	Adipose Nuclei	Adipose
32	chr1:92318000-92320800	Weak transcription	Duodenum Smooth Muscle	Duodenum
33	chr1:92318000-92320800	Weak transcription	Gastric	stomach
34	chr1:92318000-92321800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
35	chr1:92318000-92326600	Weak transcription	NHLF	lung
36	chr1:92318000-92328800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
37	chr1:92318000-92328800	Weak transcription	Fetal Lung	lung
38	chr1:92318000-92336800	Weak transcription	Sigmoid Colon	Sigmoid Colon
39	chr1:92318000-92337000	Weak transcription	Small Intestine	intestine
40	chr1:92318200-92319800	Weak transcription	Lung	lung
41	chr1:92318200-92319800	Weak transcription	Pancreas	Pancrea
42	chr1:92318200-92319800	Weak transcription	Psoas Muscle	Psoas
43	chr1:92318200-92319800	Weak transcription	NHDF-Ad	bronchial
44	chr1:92318200-92320200	Weak transcription	Fetal Heart	heart
45	chr1:92318200-92321800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr1:92318200-92329600	Weak transcription	Left Ventricle	heart
47	chr1:92318600-92320600	Strong transcription	HepG2	liver
48	chr1:92318600-92321600	Weak transcription	Right Atrium	heart
49	chr1:92318800-92320400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr1:92319200-92319800	Strong transcription	Ovary	ovary

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