Variant report

Variant	rs6722096
Chromosome Location	chr2:39559844-39559845
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:39558231..39561041-chr2:39565339..39568222,3	MCF-7	breast:

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs12105018	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs17023400	0.83[AMR][1000 genomes]
rs57107827	0.92[AMR][1000 genomes]
rs57164521	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58019817	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6706951	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6725496	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6725704	0.85[YRI][hapmap];0.92[AMR][1000 genomes]
rs6732290	0.91[YRI][hapmap];0.82[AFR][1000 genomes]
rs6759388	0.91[AMR][1000 genomes]
rs72914206	0.92[AMR][1000 genomes]
rs72925244	0.87[AFR][1000 genomes]
rs72925249	0.91[AFR][1000 genomes]
rs72925250	0.91[AFR][1000 genomes]
rs72925252	0.91[AFR][1000 genomes]
rs72925278	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72925283	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72925290	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72927103	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72927107	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72927108	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72927110	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72927119	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72927123	0.85[AMR][1000 genomes]
rs72927143	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72929164	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs72929184	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs72931129	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs72931131	0.91[AMR][1000 genomes]
rs72931135	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs72931145	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs72931150	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72931159	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72931161	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72931172	0.92[AMR][1000 genomes]
rs7566368	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs7581123	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs7585411	0.83[AMR][1000 genomes]
rs7589593	0.88[AFR][1000 genomes]
rs7592925	0.95[YRI][hapmap];0.80[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs7609233	0.95[YRI][hapmap];0.91[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:23 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv873885	chr2:39200198-39573521	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	nsv1010874	chr2:39255376-39604535	Strong transcription Flanking Active TSS Enhancers Active TSS Weak transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
3	nsv535649	chr2:39255376-39604535	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
4	nsv531346	chr2:39263225-39606367	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
5	nsv533348	chr2:39264345-39596169	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
6	nsv1014520	chr2:39270598-39596299	Enhancers Active TSS Genic enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
7	nsv535650	chr2:39270598-39596299	Enhancers Active TSS Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
8	nsv1009379	chr2:39271472-39604535	Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
9	nsv581494	chr2:39277851-39626388	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
10	nsv533456	chr2:39281834-39596298	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
11	esv1832414	chr2:39385155-39588797	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
12	esv1827292	chr2:39385155-39675339	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
13	esv1812828	chr2:39396457-39675339	Flanking Active TSS Strong transcription Active TSS Enhancers Weak transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
14	nsv833847	chr2:39410762-39604640	ZNF genes & repeats Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
15	nsv533445	chr2:39412970-39605266	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
16	esv1830024	chr2:39440552-39588797	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
17	nsv873886	chr2:39468676-39573521	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
18	nsv873887	chr2:39468676-39601889	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
19	nsv997934	chr2:39473548-39751029	Enhancers Strong transcription ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
20	esv1809158	chr2:39474679-39588797	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
21	esv1828851	chr2:39508121-39588797	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
22	nsv873888	chr2:39508830-39573521	Strong transcription Genic enhancers Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
23	esv2762497	chr2:39540753-39566724	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:101 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:39481000-39580200	Weak transcription	NHEK	skin
2	chr2:39493600-39565800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr2:39504600-39562000	Weak transcription	Psoas Muscle	Psoas
4	chr2:39504800-39565800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr2:39504800-39567200	Weak transcription	Hela-S3	cervix
6	chr2:39505400-39562400	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr2:39517600-39566400	Weak transcription	Primary T helper cells PMA-I stimulated	--
8	chr2:39519800-39562200	Weak transcription	K562	blood
9	chr2:39519800-39583000	Weak transcription	Brain Angular Gyrus	brain
10	chr2:39520000-39586200	Weak transcription	Fetal Kidney	kidney
11	chr2:39520400-39565800	Weak transcription	Rectal Smooth Muscle	rectum
12	chr2:39524000-39583600	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr2:39528200-39562800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr2:39528400-39562800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr2:39528800-39581800	Weak transcription	Brain Germinal Matrix	brain
16	chr2:39531000-39561600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
17	chr2:39534000-39586200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr2:39535400-39562600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr2:39536000-39560800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
20	chr2:39537200-39563800	Weak transcription	Spleen	Spleen
21	chr2:39538800-39572000	Weak transcription	Small Intestine	intestine
22	chr2:39539000-39563000	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr2:39539000-39583800	Weak transcription	Brain Anterior Caudate	brain
24	chr2:39539000-39586400	Weak transcription	Pancreas	Pancrea
25	chr2:39540400-39560400	Weak transcription	Rectal Mucosa Donor 29	rectum
26	chr2:39540400-39561400	Weak transcription	Fetal Brain Female	brain
27	chr2:39541000-39586400	Weak transcription	Lung	lung
28	chr2:39541400-39582200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr2:39542000-39562200	Weak transcription	Fetal Brain Male	brain
30	chr2:39542200-39561600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr2:39542200-39565600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
32	chr2:39543000-39569400	Weak transcription	HUVEC	blood vessel
33	chr2:39545400-39585800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr2:39545800-39560400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr2:39546400-39561600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr2:39548200-39562200	Weak transcription	Brain Substantia Nigra	brain
37	chr2:39549800-39561600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr2:39552000-39563000	Strong transcription	HepG2	liver
39	chr2:39552600-39562000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
40	chr2:39552600-39562200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr2:39553800-39562800	Strong transcription	HSMM	muscle
42	chr2:39553800-39569000	Weak transcription	HMEC	breast
43	chr2:39554000-39571000	Weak transcription	Primary T cells fromperipheralblood	blood
44	chr2:39554200-39562000	Weak transcription	Primary monocytes fromperipheralblood	blood
45	chr2:39554400-39562000	Weak transcription	GM12878-XiMat	blood
46	chr2:39554600-39586400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr2:39554800-39562800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr2:39554800-39563000	Strong transcription	Primary hematopoietic stem cells	blood
49	chr2:39555400-39566600	Weak transcription	Skeletal Muscle Male	skeletal muscle
50	chr2:39555400-39581200	Weak transcription	Fetal Muscle Leg	muscle

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