Variant report

Variant	rs3734262
Chromosome Location	chr6:34838577-34838578
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:34835870..34838689-chr6:34843706..34845674,2	K562	blood:
2	chr6:34837346..34838981-chr6:34850648..34853394,2	K562	blood:
3	chr6:34837193..34840409-chr6:34855219..34858367,4	K562	blood:
4	chr6:34837193..34840268-chr6:34856468..34858367,3	K562	blood:

Variant related genes	Relation type
ENSG00000064995	Chromatin interaction
ENSG00000064999	Chromatin interaction

Extended variants
information (count: 70 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs10947536	0.91[CHB][hapmap];0.85[CHD][hapmap];0.91[JPT][hapmap]
rs12176092	0.80[CEU][hapmap]
rs12212217	0.82[CHB][hapmap]
rs13218101	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13219624	0.95[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs13220394	0.90[LWK][hapmap]
rs1555107	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs16895035	0.83[LWK][hapmap];0.81[MKK][hapmap]
rs16895362	0.80[CEU][hapmap]
rs16895467	0.80[CEU][hapmap]
rs16896390	0.80[CEU][hapmap];0.82[CHB][hapmap];0.84[CHD][hapmap];0.82[GIH][hapmap];0.82[JPT][hapmap];0.91[MEX][hapmap]
rs1737727	0.91[CHB][hapmap];0.85[CHD][hapmap];0.86[JPT][hapmap];0.88[ASN][1000 genomes]
rs2140418	0.82[CHB][hapmap];0.85[CHD][hapmap]
rs2177381	0.91[CHB][hapmap];0.85[CHD][hapmap];0.91[JPT][hapmap]
rs2273006	1.00[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs2293242	0.91[CHB][hapmap];0.85[CHD][hapmap];0.91[JPT][hapmap]
rs2473613	0.95[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs2504162	0.95[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs2985	1.00[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs3734259	0.83[LWK][hapmap];0.81[MKK][hapmap]
rs3734260	0.80[CEU][hapmap]
rs3734263	0.80[CEU][hapmap]
rs3756859	0.81[MKK][hapmap]
rs3800449	0.80[CEU][hapmap]
rs3800451	0.95[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs3800453	0.83[LWK][hapmap];0.81[MKK][hapmap]
rs4646940	0.98[ASN][1000 genomes]
rs4646944	0.98[ASN][1000 genomes]
rs6457792	0.87[LWK][hapmap]
rs6905468	1.00[ASW][hapmap];1.00[CEU][hapmap];0.95[CHB][hapmap];0.97[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.83[LWK][hapmap];1.00[MEX][hapmap];0.92[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6907619	1.00[ASW][hapmap];0.95[CHB][hapmap];0.95[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.84[LWK][hapmap];1.00[MEX][hapmap];0.92[MKK][hapmap];0.83[TSI][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6918183	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6918872	0.95[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs6932857	0.91[CHB][hapmap];0.91[JPT][hapmap]
rs7739991	0.93[ASN][1000 genomes]
rs7756405	0.87[LWK][hapmap]
rs7757211	0.93[ASN][1000 genomes]
rs847847	0.88[ASN][1000 genomes]
rs847848	0.95[CHB][hapmap];0.90[CHD][hapmap];0.91[JPT][hapmap];0.88[ASN][1000 genomes]
rs9296139	0.95[CHB][hapmap];0.86[CHD][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs9348954	0.80[CEU][hapmap]
rs9357185	0.87[AFR][1000 genomes]
rs9357186	0.80[CEU][hapmap]
rs9357188	0.95[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs9366870	0.87[AFR][1000 genomes]
rs9368834	1.00[ASW][hapmap];1.00[CEU][hapmap];0.95[CHB][hapmap];0.97[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.81[LWK][hapmap];1.00[MEX][hapmap];0.92[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9368836	0.93[ASN][1000 genomes]
rs9368842	0.80[CEU][hapmap]
rs9380466	0.81[MKK][hapmap]
rs9380467	0.81[MKK][hapmap]
rs9394252	0.94[ASN][1000 genomes]
rs9394257	0.80[CEU][hapmap]
rs9394259	0.80[CEU][hapmap]
rs9462027	0.87[LWK][hapmap]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1022844	chr6:34317219-35060519	Weak transcription Genic enhancers Enhancers Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
2	nsv538195	chr6:34317219-35060519	Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
3	nsv885785	chr6:34404636-34874002	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
4	nsv885793	chr6:34520267-34886436	Active TSS Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
5	esv2763967	chr6:34566255-34925463	Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
6	nsv1020710	chr6:34607214-34890143	Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
7	nsv870010	chr6:34713359-34880048	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	33 gene(s)	inside rSNPs	diseases
8	nsv1025374	chr6:34723723-34887316	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	33 gene(s)	inside rSNPs	diseases
9	nsv462905	chr6:34728253-34886436	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	30 gene(s)	inside rSNPs	diseases
10	nsv602906	chr6:34728253-34886436	Strong transcription Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	30 gene(s)	inside rSNPs	diseases
11	nsv1028363	chr6:34733071-34859045	Weak transcription Active TSS Strong transcription Enhancers Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	30 gene(s)	inside rSNPs	diseases
12	nsv1015792	chr6:34741917-34887316	Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats 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 miRNA target site	30 gene(s)	inside rSNPs	diseases
13	nsv1021733	chr6:34751052-34887316	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	30 gene(s)	inside rSNPs	diseases
14	nsv1026121	chr6:34786887-34961360	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS 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 miRNA target site	19 gene(s)	inside rSNPs	diseases
15	nsv885797	chr6:34791027-34980601	Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	18 gene(s)	inside rSNPs	diseases
16	nsv1033135	chr6:34802652-34957093	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:34779400-34841000	Weak transcription	NH-A	brain
2	chr6:34786600-34838800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr6:34816800-34853600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr6:34817400-34851200	Strong transcription	Fetal Thymus	thymus
5	chr6:34818600-34853400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr6:34819000-34842600	Strong transcription	Fetal Intestine Small	intestine
7	chr6:34820200-34855000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr6:34821000-34854600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr6:34822800-34849400	Strong transcription	Monocytes-CD14+_RO01746	blood
10	chr6:34823000-34851600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr6:34823400-34839400	Weak transcription	HMEC	breast
12	chr6:34825400-34839800	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr6:34825800-34847600	Weak transcription	NHDF-Ad	bronchial
14	chr6:34826000-34840000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
15	chr6:34826800-34838800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
16	chr6:34826800-34839000	Weak transcription	NHEK	skin
17	chr6:34827000-34838800	Weak transcription	Pancreatic Islets	Pancreatic Islet
18	chr6:34827200-34840200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
19	chr6:34827400-34838600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr6:34827400-34839000	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr6:34827400-34839400	Weak transcription	Esophagus	oesophagus
22	chr6:34827600-34838600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr6:34827600-34838600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr6:34827600-34838600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr6:34827600-34841200	Weak transcription	Stomach Mucosa	stomach
26	chr6:34827800-34838800	Weak transcription	Spleen	Spleen
27	chr6:34828000-34839000	Weak transcription	Right Ventricle	heart
28	chr6:34828200-34838600	Weak transcription	Aorta	Aorta
29	chr6:34828800-34838800	Weak transcription	Fetal Brain Male	brain
30	chr6:34830000-34855000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr6:34830800-34848400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
32	chr6:34831400-34849400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr6:34834400-34840200	Weak transcription	HUVEC	blood vessel
34	chr6:34834400-34849000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr6:34834400-34851200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr6:34834400-34853600	Strong transcription	Primary T helper cells fromperipheralblood	blood
37	chr6:34834600-34841600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr6:34834600-34843600	Strong transcription	Rectal Mucosa Donor 31	rectum
39	chr6:34834600-34843800	Strong transcription	K562	blood
40	chr6:34834600-34849800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr6:34834800-34850200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr6:34835000-34839200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
43	chr6:34835000-34841400	Strong transcription	Brain Germinal Matrix	brain
44	chr6:34835000-34841800	Strong transcription	HUES64 Cell Line	embryonic stem cell
45	chr6:34835000-34842800	Strong transcription	Fetal Stomach	stomach
46	chr6:34835000-34843200	Strong transcription	Fetal Intestine Large	intestine
47	chr6:34835000-34843200	Strong transcription	Lung	lung
48	chr6:34835000-34843600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr6:34835000-34843800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
50	chr6:34835000-34846000	Strong transcription	HepG2	liver

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