Variant report

Variant	rs2092649
Chromosome Location	chr6:88205458-88205459
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:88182233..88184298-chr6:88203601..88206003,2	MCF-7	breast:
2	chr6:88200036..88203447-chr6:88205362..88210023,5	MCF-7	breast:

Variant related genes	Relation type
ENSG00000164414	Chromatin interaction

Extended variants
information (count: 38 )
Associated
traits (count: 1 )

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

rs_ID	r²[population]
rs11962148	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12524203	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12524205	0.84[ASN][1000 genomes]
rs13195393	0.84[ASN][1000 genomes]
rs16879893	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2143890	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2246057	0.90[ASN][1000 genomes]
rs2268995	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2268996	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2300898	0.84[ASN][1000 genomes]
rs2300899	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2300900	0.84[ASN][1000 genomes]
rs2300904	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2300907	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2300908	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3778671	0.80[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3818057	0.87[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs58785365	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6903332	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6927171	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6928057	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6931177	0.84[ASN][1000 genomes]
rs7383567	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7761943	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9444509	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9450708	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9450709	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9450711	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9450716	0.80[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9450717	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9450719	0.84[ASN][1000 genomes]
rs9450721	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[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	nsv1018155	chr6:88049729-88272862	Strong transcription Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv830722	chr6:88054186-88223625	Enhancers Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv1031961	chr6:88110401-88367006	Weak transcription Strong transcription Flanking Active TSS Active TSS Enhancers 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 lncRNA	21 gene(s)	inside rSNPs	diseases
4	nsv1031460	chr6:88153079-88410050	Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
5	nsv1026482	chr6:88164934-88409728	Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers 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	21 gene(s)	inside rSNPs	diseases
6	nsv1027706	chr6:88168987-88409728	Genic enhancers Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	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
rs2092649	SLC35A1	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:108 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:88183600-88212800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr6:88183600-88226000	Weak transcription	Gastric	stomach
3	chr6:88183800-88210800	Weak transcription	Adipose Nuclei	Adipose
4	chr6:88183800-88211000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr6:88183800-88211000	Weak transcription	Brain Anterior Caudate	brain
6	chr6:88183800-88211000	Weak transcription	Thymus	Thymus
7	chr6:88183800-88211800	Weak transcription	Rectal Smooth Muscle	rectum
8	chr6:88183800-88212000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr6:88183800-88212600	Weak transcription	Psoas Muscle	Psoas
10	chr6:88183800-88216400	Weak transcription	K562	blood
11	chr6:88183800-88219800	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr6:88183800-88221000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
13	chr6:88183800-88221000	Weak transcription	Fetal Kidney	kidney
14	chr6:88183800-88225400	Weak transcription	Aorta	Aorta
15	chr6:88183800-88227400	Weak transcription	Right Ventricle	heart
16	chr6:88184000-88210800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
17	chr6:88184000-88211000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
18	chr6:88184000-88211000	Weak transcription	Stomach Smooth Muscle	stomach
19	chr6:88184000-88218600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr6:88184000-88218600	Weak transcription	Brain Angular Gyrus	brain
21	chr6:88184000-88218800	Weak transcription	Brain Germinal Matrix	brain
22	chr6:88184000-88219800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
23	chr6:88184000-88221000	Weak transcription	Colon Smooth Muscle	Colon
24	chr6:88184000-88224200	Weak transcription	Hela-S3	cervix
25	chr6:88184200-88211000	Weak transcription	NHDF-Ad	bronchial
26	chr6:88184200-88214800	Weak transcription	Fetal Brain Male	brain
27	chr6:88184400-88211200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
28	chr6:88184400-88211800	Weak transcription	Brain Substantia Nigra	brain
29	chr6:88185800-88211400	Weak transcription	Brain Inferior Temporal Lobe	brain
30	chr6:88186000-88211400	Weak transcription	Muscle Satellite Cultured Cells	--
31	chr6:88187800-88210800	Weak transcription	Primary T helper cells fromperipheralblood	blood
32	chr6:88188400-88208200	Weak transcription	Sigmoid Colon	Sigmoid Colon
33	chr6:88188400-88211000	Weak transcription	Primary T helper cells PMA-I stimulated	--
34	chr6:88188600-88221600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
35	chr6:88188800-88210800	Weak transcription	Left Ventricle	heart
36	chr6:88189200-88211200	Weak transcription	Primary hematopoietic stem cells	blood
37	chr6:88191200-88227400	Weak transcription	Spleen	Spleen
38	chr6:88192400-88210200	Weak transcription	Primary T cells fromperipheralblood	blood
39	chr6:88193600-88214200	Weak transcription	HSMMtube	muscle
40	chr6:88193600-88227600	Weak transcription	Pancreas	Pancrea
41	chr6:88193800-88210600	Weak transcription	Placenta	Placenta
42	chr6:88193800-88211000	Weak transcription	Skeletal Muscle Female	skeletal muscle
43	chr6:88193800-88220400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr6:88193800-88221000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
45	chr6:88193800-88221400	Weak transcription	Ovary	ovary
46	chr6:88193800-88227400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr6:88194000-88211000	Weak transcription	Brain Hippocampus Middle	brain
48	chr6:88194000-88211000	Weak transcription	Duodenum Mucosa	Duodenum
49	chr6:88194000-88211000	Weak transcription	Fetal Lung	lung
50	chr6:88194000-88211000	Weak transcription	HMEC	breast

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