Variant report

Variant	rs11773545
Chromosome Location	chr7:7196878-7196879
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs11762665	0.92[CHB][hapmap];0.88[CHD][hapmap];0.83[LWK][hapmap];0.86[MEX][hapmap];0.87[YRI][hapmap];0.80[AMR][1000 genomes]
rs11765714	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11770958	1.00[CEU][hapmap];0.91[CHB][hapmap];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11773401	0.92[CHB][hapmap];1.00[YRI][hapmap];0.80[AMR][1000 genomes]
rs11974698	1.00[ASW][hapmap];1.00[CEU][hapmap];0.92[CHB][hapmap];0.88[CHD][hapmap];1.00[GIH][hapmap];0.84[TSI][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12702586	0.84[ASW][hapmap];0.92[CHB][hapmap];0.91[CHD][hapmap];1.00[LWK][hapmap];0.86[MEX][hapmap];0.90[MKK][hapmap];0.82[TSI][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs13224188	0.93[AFR][1000 genomes]
rs13229375	0.83[AFR][1000 genomes]
rs13243458	0.83[AFR][1000 genomes]
rs1432196	0.82[ASN][1000 genomes]
rs1432199	0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs35356155	0.93[AFR][1000 genomes]
rs35663821	0.93[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1015277	chr7:6705439-7303195	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
2	nsv1023133	chr7:6854098-7516700	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
3	nsv869091	chr7:6927461-7567820	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
4	nsv428160	chr7:6936949-7219553	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
5	nsv1020929	chr7:6954959-7232920	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	39 gene(s)	inside rSNPs	diseases
6	nsv949293	chr7:6990891-7711883	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
7	nsv887469	chr7:7036939-7205749	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
8	nsv464300	chr7:7040176-7368699	Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
9	nsv606033	chr7:7040176-7368699	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
10	nsv1015553	chr7:7053923-7201291	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
11	nsv538719	chr7:7053923-7201291	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
12	nsv1016369	chr7:7053923-7375567	Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
13	nsv1023788	chr7:7053923-7407783	Weak transcription Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
14	nsv538720	chr7:7053923-7407783	Enhancers Weak transcription Active TSS Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
15	nsv1032813	chr7:7053923-7497484	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
16	nsv1030246	chr7:7053923-7569633	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
17	nsv1019498	chr7:7053923-7668373	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
18	nsv538721	chr7:7053923-7668373	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
19	nsv1032974	chr7:7145831-7393218	Flanking Active TSS Strong transcription Enhancers Weak transcription Genic enhancers ZNF genes & repeats Active TSS 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	33 gene(s)	inside rSNPs	diseases
20	nsv1026758	chr7:7187491-8075259	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	84 gene(s)	inside rSNPs	diseases
21	nsv508445	chr7:7190518-7261098	Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
22	nsv519087	chr7:7196848-7200881	Active TSS Flanking Active TSS Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	n/a	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs11773545	C1GALT1	cis	cerebellum	SCAN
rs11773545	C1GALT1	cis	parietal	SCAN
rs11773545	ACTB	cis	cerebellum	SCAN
rs11773545	C1GALT1	cis	multi-tissue	Pritchard

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:7189200-7199600	Weak transcription	K562	blood
2	chr7:7195800-7197000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr7:7195800-7197000	Enhancers	GM12878-XiMat	blood
4	chr7:7196200-7198200	Flanking Active TSS	Osteobl	bone
5	chr7:7196200-7200200	Flanking Active TSS	Primary T cells from cord blood	blood
6	chr7:7196400-7197000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr7:7196400-7197000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr7:7196400-7197000	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
9	chr7:7196400-7197000	Enhancers	Thymus	Thymus
10	chr7:7196400-7197000	Enhancers	NHEK	skin
11	chr7:7196400-7197600	Enhancers	Stomach Mucosa	stomach
12	chr7:7196400-7197800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
13	chr7:7196400-7197800	Flanking Active TSS	HepG2	liver
14	chr7:7196400-7198000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
15	chr7:7196400-7198000	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
16	chr7:7196400-7198000	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
17	chr7:7196400-7198000	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
18	chr7:7196400-7198000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr7:7196400-7198000	Enhancers	Placenta Amnion	Placenta Amnion
20	chr7:7196400-7198000	Enhancers	Small Intestine	intestine
21	chr7:7196400-7198400	Enhancers	Primary hematopoietic stem cells	blood
22	chr7:7196400-7200600	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr7:7196600-7197000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
24	chr7:7196600-7197000	Enhancers	HSMM	muscle
25	chr7:7196600-7198000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
26	chr7:7196600-7198000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr7:7196600-7198000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr7:7196600-7200600	Flanking Active TSS	Primary B cells from cord blood	blood
29	chr7:7196800-7197000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr7:7196800-7197000	Enhancers	Primary neutrophils fromperipheralblood	blood
31	chr7:7196800-7197000	Flanking Active TSS	Primary B cells from peripheral blood	blood
32	chr7:7196800-7197000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
33	chr7:7196800-7197000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
34	chr7:7196800-7197000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
35	chr7:7196800-7197000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr7:7196800-7197000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr7:7196800-7197000	Flanking Active TSS	Fetal Thymus	thymus
38	chr7:7196800-7197000	Enhancers	Rectal Mucosa Donor 31	rectum
39	chr7:7196800-7197000	Enhancers	Sigmoid Colon	Sigmoid Colon
40	chr7:7196800-7197000	Flanking Active TSS	HMEC	breast
41	chr7:7196800-7197000	Flanking Active TSS	NHDF-Ad	bronchial
42	chr7:7196800-7197000	Flanking Active TSS	NHLF	lung
43	chr7:7196800-7197200	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
44	chr7:7196800-7197200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr7:7196800-7197200	Enhancers	Duodenum Mucosa	Duodenum
46	chr7:7196800-7197200	Active TSS	HSMMtube	muscle
47	chr7:7196800-7197400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
48	chr7:7196800-7197400	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr7:7196800-7197400	Active TSS	Dnd41	blood
50	chr7:7196800-7198000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung

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