Variant report

Variant	rs2123279
Chromosome Location	chr16:80658749-80658750
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr16:80658450..80660494-chr16:80660496..80663091,2	MCF-7	breast:
2	chr16:80653589..80657400-chr16:80657593..80661612,3	K562	blood:
3	chr16:80657007..80659717-chr16:80664386..80666332,2	K562	blood:
4	chr16:80654014..80661253-chr16:80836600..80840694,9	MCF-7	breast:
5	chr16:80657950..80660118-chr16:80836861..80838846,2	MCF-7	breast:
6	chr16:80653485..80655242-chr16:80656903..80659850,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000166446	Chromatin interaction
ENSG00000260064	Chromatin interaction

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs1109546	0.85[CHB][hapmap];0.95[JPT][hapmap]
rs12448290	0.82[CHB][hapmap];0.95[JPT][hapmap]
rs13329877	0.86[CHB][hapmap];0.96[JPT][hapmap]
rs2123280	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs2123281	0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4325579	0.82[AMR][1000 genomes]
rs4586445	0.85[EUR][1000 genomes]
rs4888100	1.00[CHB][hapmap];0.95[JPT][hapmap];0.98[ASN][1000 genomes]
rs4888101	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs4888102	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs4888103	0.89[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs4889166	0.95[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs4889167	0.94[CHB][hapmap];0.94[JPT][hapmap];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4889168	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4889169	0.86[CHB][hapmap];0.95[JPT][hapmap]
rs4889170	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4889171	0.90[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs4889172	0.90[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs4889173	0.82[YRI][hapmap];0.83[AFR][1000 genomes]
rs4889174	0.83[AFR][1000 genomes]
rs4889176	0.90[CEU][hapmap];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4889177	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4889178	0.85[EUR][1000 genomes]
rs4889179	0.93[AFR][1000 genomes];0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4889180	0.90[CEU][hapmap];0.84[EUR][1000 genomes]
rs4889181	0.93[AFR][1000 genomes];0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs56713233	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs57872556	0.85[EUR][1000 genomes]
rs59946023	0.84[EUR][1000 genomes]
rs60236050	0.85[EUR][1000 genomes]
rs60596417	0.89[EUR][1000 genomes]
rs60992426	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs74028350	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs74028368	0.85[EUR][1000 genomes]
rs8057859	0.86[CHB][hapmap];0.95[JPT][hapmap]
rs8059592	0.91[CEU][hapmap]
rs9922043	0.89[EUR][1000 genomes]
rs9924170	0.90[EUR][1000 genomes]
rs9927571	0.95[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1060621	chr16:80532848-80980616	Weak transcription Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
2	nsv542989	chr16:80532848-80980616	Enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
3	nsv1056083	chr16:80636184-80666779	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1063971	chr16:80640278-80663092	Strong transcription Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv1063761	chr16:80640278-80663665	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv1055196	chr16:80647550-80672417	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv1057562	chr16:80650768-80675842	Strong transcription Weak transcription Active TSS Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv1058764	chr16:80656966-80707848	Active TSS Flanking Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:80630600-80668000	Weak transcription	Fetal Kidney	kidney
2	chr16:80634200-80663600	Weak transcription	Brain Anterior Caudate	brain
3	chr16:80640600-80662200	Weak transcription	Primary T cells from cord blood	blood
4	chr16:80640600-80662600	Weak transcription	Primary T helper cells fromperipheralblood	blood
5	chr16:80640800-80663800	Weak transcription	Primary T helper cells PMA-I stimulated	--
6	chr16:80640800-80669200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
7	chr16:80642200-80668200	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr16:80642800-80663800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
9	chr16:80644200-80666200	Weak transcription	Brain Substantia Nigra	brain
10	chr16:80646400-80662200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr16:80646400-80662200	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr16:80646600-80687800	Weak transcription	Pancreas	Pancrea
13	chr16:80647000-80665000	Weak transcription	Gastric	stomach
14	chr16:80650000-80661800	Weak transcription	Muscle Satellite Cultured Cells	--
15	chr16:80650400-80659800	Strong transcription	Hela-S3	cervix
16	chr16:80653200-80668200	Weak transcription	Primary T cells fromperipheralblood	blood
17	chr16:80653600-80662200	Weak transcription	Monocytes-CD14+_RO01746	blood
18	chr16:80653600-80666800	Weak transcription	Esophagus	oesophagus
19	chr16:80653600-80667400	Weak transcription	Fetal Stomach	stomach
20	chr16:80653800-80662000	Weak transcription	Duodenum Mucosa	Duodenum
21	chr16:80654400-80662000	Weak transcription	Liver	Liver
22	chr16:80654400-80667800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chr16:80654400-80668800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
24	chr16:80654800-80662200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
25	chr16:80655000-80661800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr16:80655000-80662400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr16:80657200-80668000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr16:80657800-80658800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
29	chr16:80658000-80661600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
30	chr16:80658000-80667200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr16:80658000-80668200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr16:80658200-80661800	Weak transcription	Aorta	Aorta
33	chr16:80658200-80662000	Weak transcription	Spleen	Spleen
34	chr16:80658400-80658800	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr16:80658400-80658800	Weak transcription	Placenta	Placenta
36	chr16:80658400-80666600	Weak transcription	HUVEC	blood vessel

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