Variant report

Variant	rs7761779
Chromosome Location	chr6:26262306-26262307
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 72 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs11751564	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11751567	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11751978	0.85[CEU][hapmap]
rs11752014	0.85[CEU][hapmap]
rs11753610	1.00[JPT][hapmap]
rs11754168	0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11754384	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.90[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.89[YRI][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11754746	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11755795	1.00[CEU][hapmap];1.00[YRI][hapmap];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11756428	0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11757214	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11757736	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11759682	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.82[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.89[YRI][hapmap];0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11962642	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16891523	0.85[CEU][hapmap]
rs16891525	0.85[CEU][hapmap]
rs1883214	0.85[CEU][hapmap]
rs2006005	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2006006	0.98[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs34434694	0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3734534	1.00[JPT][hapmap]
rs3823157	1.00[CEU][hapmap];1.00[CHD][hapmap];0.91[MEX][hapmap];0.94[TSI][hapmap];0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs41266829	0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs41266831	0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4631273	0.85[CEU][hapmap]
rs56768418	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs57145038	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs57530446	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs59225416	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs60122474	0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60228626	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61082103	0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61213538	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs61625476	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6901243	1.00[CEU][hapmap];1.00[CHD][hapmap];0.91[MEX][hapmap];0.94[TSI][hapmap];0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6914596	0.85[CEU][hapmap]
rs6916643	1.00[CEU][hapmap];1.00[YRI][hapmap];0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6938696	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs73393491	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73393492	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73395313	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs73395314	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs73397320	0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73397336	0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73397339	0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73397347	0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73397364	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs73399366	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73399394	0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73401208	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs73401228	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73401231	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73401236	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73401243	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7740838	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7773163	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9688734	0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029920	chr6:25638507-26585842	Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
2	nsv538162	chr6:25638507-26585842	Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
3	nsv1030351	chr6:25813178-26352046	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1189 gene(s)	inside rSNPs	diseases
4	nsv1023453	chr6:25853830-26528250	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1201 gene(s)	inside rSNPs	diseases
5	nsv1025237	chr6:25874326-26280867	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1166 gene(s)	inside rSNPs	diseases
6	nsv538163	chr6:25874326-26280867	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1166 gene(s)	inside rSNPs	diseases
7	nsv428137	chr6:25987413-26351920	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1181 gene(s)	inside rSNPs	diseases
8	nsv916992	chr6:25991630-26280921	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1159 gene(s)	inside rSNPs	diseases
9	nsv1028232	chr6:26005449-26319756	Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1171 gene(s)	inside rSNPs	diseases
10	nsv870314	chr6:26008435-26280807	Flanking Active TSS Enhancers Active TSS Genic enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1151 gene(s)	inside rSNPs	diseases
11	nsv1023457	chr6:26014014-26305407	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1170 gene(s)	inside rSNPs	diseases
12	nsv1023979	chr6:26026870-26287399	Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1113 gene(s)	inside rSNPs	diseases
13	nsv1015782	chr6:26026870-26323895	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1114 gene(s)	inside rSNPs	diseases
14	nsv1018665	chr6:26026870-26352046	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1116 gene(s)	inside rSNPs	diseases
15	nsv601173	chr6:26239404-26322524	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	184 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs7761779	ZKSCAN4	cis	cerebellum	SCAN
rs7761779	HIST1H3E	cis	cerebellum	SCAN
rs7761779	HIST1H3E	cis	parietal	SCAN
rs7761779	ZNF165	cis	parietal	SCAN

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:26252400-26271200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr6:26253800-26265400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr6:26253800-26271000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr6:26254200-26269200	Weak transcription	Fetal Stomach	stomach
5	chr6:26255000-26269400	Weak transcription	Primary hematopoietic stem cells	blood
6	chr6:26255600-26270400	Weak transcription	Primary B cells from cord blood	blood
7	chr6:26255600-26270400	Weak transcription	Primary T cells from cord blood	blood
8	chr6:26255800-26269400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr6:26258200-26269200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr6:26258800-26264600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr6:26258800-26269200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr6:26259000-26264800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr6:26259000-26264800	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr6:26259000-26270000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr6:26259200-26264600	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr6:26259200-26264600	Weak transcription	HUES6 Cell Line	embryonic stem cell
17	chr6:26259200-26264600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr6:26259200-26264600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr6:26259200-26264800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr6:26259200-26269000	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr6:26259200-26269000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr6:26259200-26269200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr6:26260000-26262400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
24	chr6:26260400-26262400	Enhancers	Primary neutrophils fromperipheralblood	blood
25	chr6:26260600-26269200	Weak transcription	Thymus	Thymus
26	chr6:26260800-26262600	Enhancers	Fetal Intestine Large	intestine
27	chr6:26260800-26262600	Enhancers	Fetal Intestine Small	intestine
28	chr6:26260800-26268400	Weak transcription	Fetal Thymus	thymus
29	chr6:26261000-26262400	Enhancers	HepG2	liver
30	chr6:26261400-26269000	Weak transcription	Stomach Mucosa	stomach
31	chr6:26261800-26263200	Enhancers	Primary monocytes fromperipheralblood	blood
32	chr6:26262000-26266600	Weak transcription	K562	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links