Variant report

Variant	rs6725784
Chromosome Location	chr2:39539427-39539428
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:39531304..39535719-chr2:39536825..39539603,4	K562	blood:

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

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

rs_ID	r²[population]
rs10490305	0.89[ASW][hapmap];1.00[CEU][hapmap];1.00[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.96[LWK][hapmap];0.81[MKK][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11886110	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11898704	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.96[LWK][hapmap];0.81[MKK][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11902188	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17023620	1.00[CEU][hapmap];0.92[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17038958	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2708227	1.00[JPT][hapmap]
rs3770661	0.83[ASN][1000 genomes]
rs55961227	0.84[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs56361338	0.83[ASN][1000 genomes]
rs56850142	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs56928728	0.87[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs58005382	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs58824151	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs59459399	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs59707152	0.90[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs61219633	0.84[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs6544206	1.00[JPT][hapmap]
rs6544225	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6712399	1.00[ASW][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];0.91[YRI][hapmap];0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs6723987	0.82[AFR][1000 genomes]
rs6727395	1.00[JPT][hapmap];0.91[YRI][hapmap];0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs6731330	1.00[JPT][hapmap]
rs6751506	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];0.92[YRI][hapmap];0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs73923836	0.83[ASN][1000 genomes]
rs73923844	1.00[AFR][1000 genomes]
rs73923847	0.92[ASN][1000 genomes]
rs73923848	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73923887	0.84[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs73923888	0.84[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs73923889	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs73923895	0.85[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs73924810	0.83[ASN][1000 genomes]
rs73924815	0.83[ASN][1000 genomes]
rs73924816	0.83[ASN][1000 genomes]
rs73924817	0.83[ASN][1000 genomes]
rs73924818	0.83[ASN][1000 genomes]
rs7591563	0.81[AFR][1000 genomes]
rs7595047	0.83[ASN][1000 genomes]
rs7595102	1.00[JPT][hapmap]
rs7599017	0.82[AFR][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	nsv581493	chr2:39277851-39547575	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	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
19	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
20	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
21	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
22	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
23	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

No data

Chromatin state (count:115 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:39478600-39543400	Weak transcription	Stomach Mucosa	stomach
2	chr2:39481000-39580200	Weak transcription	NHEK	skin
3	chr2:39493600-39565800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr2:39494000-39553000	Weak transcription	GM12878-XiMat	blood
5	chr2:39504600-39540000	Weak transcription	Right Ventricle	heart
6	chr2:39504600-39562000	Weak transcription	Psoas Muscle	Psoas
7	chr2:39504800-39541600	Weak transcription	Fetal Brain Male	brain
8	chr2:39504800-39565800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr2:39504800-39567200	Weak transcription	Hela-S3	cervix
10	chr2:39505400-39556800	Weak transcription	Thymus	Thymus
11	chr2:39505400-39557200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr2:39505400-39562400	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr2:39505600-39540000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
14	chr2:39513600-39555000	Weak transcription	Primary B cells from cord blood	blood
15	chr2:39514400-39539800	Weak transcription	A549	lung
16	chr2:39514400-39541800	Weak transcription	HUVEC	blood vessel
17	chr2:39516200-39557600	Weak transcription	Gastric	stomach
18	chr2:39517200-39552400	Weak transcription	HMEC	breast
19	chr2:39517600-39566400	Weak transcription	Primary T helper cells PMA-I stimulated	--
20	chr2:39519000-39555200	Weak transcription	Fetal Thymus	thymus
21	chr2:39519800-39553000	Weak transcription	Primary monocytes fromperipheralblood	blood
22	chr2:39519800-39555400	Weak transcription	Fetal Heart	heart
23	chr2:39519800-39562200	Weak transcription	K562	blood
24	chr2:39519800-39583000	Weak transcription	Brain Angular Gyrus	brain
25	chr2:39520000-39556600	Weak transcription	H1 Cell Line	embryonic stem cell
26	chr2:39520000-39586200	Weak transcription	Fetal Kidney	kidney
27	chr2:39520200-39539800	Weak transcription	Fetal Brain Female	brain
28	chr2:39520200-39553200	Weak transcription	Primary T helper cells fromperipheralblood	blood
29	chr2:39520200-39555200	Weak transcription	Ovary	ovary
30	chr2:39520400-39539800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr2:39520400-39540600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
32	chr2:39520400-39565800	Weak transcription	Rectal Smooth Muscle	rectum
33	chr2:39521200-39541000	Weak transcription	Skeletal Muscle Female	skeletal muscle
34	chr2:39524000-39583600	Weak transcription	Brain Inferior Temporal Lobe	brain
35	chr2:39525200-39553400	Weak transcription	Primary T cells fromperipheralblood	blood
36	chr2:39526200-39540000	Weak transcription	Left Ventricle	heart
37	chr2:39528000-39542000	Weak transcription	Brain Hippocampus Middle	brain
38	chr2:39528200-39551800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
39	chr2:39528200-39562800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr2:39528400-39541800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
41	chr2:39528400-39562800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr2:39528800-39581800	Weak transcription	Brain Germinal Matrix	brain
43	chr2:39529400-39545600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr2:39531000-39561600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr2:39532400-39541600	Weak transcription	Primary hematopoietic stem cells	blood
46	chr2:39532600-39539800	Strong transcription	HSMM	muscle
47	chr2:39533200-39541000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr2:39533600-39555000	Weak transcription	Brain Cingulate Gyrus	brain
49	chr2:39534000-39586200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr2:39534200-39540800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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