Variant report

Variant	rs9467684
Chromosome Location	chr6:26162679-26162680
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr6:26156238-26163035	K562	blood:	n/a	n/a
2	POLR2A	chr6:26162068-26164788	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:26160979..26163905-chr6:26498112..26500480,2	K562	blood:
2	chr6:26161523..26164154-chr6:26581877..26584576,2	K562	blood:
3	chr6:26019525..26036768-chr6:26154463..26163826,38	MCF-7	breast:

Variant related genes	Relation type
LARP1P1	TF binding region
ENSG00000137259	Chromatin interaction
ENSG00000124693	Chromatin interaction
ENSG00000198366	Chromatin interaction
ENSG00000124529	Chromatin interaction
ENSG00000196176	Chromatin interaction

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs1045537	1.00[CHB][hapmap]
rs10484433	1.00[CHB][hapmap]
rs10484435	1.00[CHB][hapmap]
rs12111009	1.00[JPT][hapmap]
rs13192365	1.00[CHB][hapmap]
rs13196552	1.00[CHB][hapmap]
rs13200797	1.00[CHB][hapmap]
rs13201821	1.00[CHB][hapmap]
rs13206501	1.00[CHB][hapmap]
rs13214280	1.00[CHB][hapmap]
rs13220395	1.00[CHB][hapmap]
rs16891235	1.00[CHB][hapmap]
rs16891261	1.00[CHB][hapmap]
rs16891264	1.00[CHB][hapmap]
rs16891315	1.00[CHB][hapmap]
rs16891334	1.00[CHB][hapmap]
rs2298091	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs3734528	1.00[CHB][hapmap]
rs4476815	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs73393441	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73393443	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73393463	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7762193	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9461236	0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9461237	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.94[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9461238	0.90[EUR][1000 genomes]
rs9461239	1.00[CEU][hapmap];1.00[MEX][hapmap];0.83[YRI][hapmap];0.90[EUR][1000 genomes]
rs9461241	1.00[CEU][hapmap];0.83[YRI][hapmap]
rs9467682	0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9467688	1.00[CEU][hapmap];0.83[YRI][hapmap];0.90[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:20 , 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	nsv1028456	chr6:25984457-26174993	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	873 gene(s)	inside rSNPs	diseases
8	nsv538165	chr6:25984457-26174993	Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	873 gene(s)	inside rSNPs	diseases
9	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
10	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
11	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
12	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
13	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
14	nsv1025493	chr6:26026870-26223838	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1001 gene(s)	inside rSNPs	diseases
15	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
16	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
17	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
18	nsv482348	chr6:26082709-26261136	Enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	799 gene(s)	inside rSNPs	diseases
19	nsv518431	chr6:26148311-26211368	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	521 gene(s)	inside rSNPs	diseases
20	nsv526456	chr6:26148311-26211368	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	521 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:94 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:26158800-26164400	Weak transcription	Spleen	Spleen
2	chr6:26159800-26164400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr6:26159800-26171800	Weak transcription	Lung	lung
4	chr6:26160000-26163000	Active TSS	Brain Germinal Matrix	brain
5	chr6:26160000-26163600	Weak transcription	Fetal Muscle Trunk	muscle
6	chr6:26160000-26171800	Weak transcription	Ovary	ovary
7	chr6:26160200-26162800	Weak transcription	Fetal Stomach	stomach
8	chr6:26160200-26165000	Weak transcription	Right Atrium	heart
9	chr6:26160200-26170400	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr6:26160200-26171600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr6:26160200-26171600	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr6:26160400-26163800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr6:26160400-26165400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr6:26160400-26171200	Weak transcription	Osteobl	bone
15	chr6:26160400-26171400	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr6:26160400-26171600	Weak transcription	Right Ventricle	heart
17	chr6:26160400-26171600	Weak transcription	HSMMtube	muscle
18	chr6:26160400-26171800	Weak transcription	Esophagus	oesophagus
19	chr6:26160600-26162800	Enhancers	Primary T killer memory cells from peripheral blood	blood
20	chr6:26160600-26162800	Enhancers	Fetal Intestine Large	intestine
21	chr6:26160600-26162800	Weak transcription	Rectal Mucosa Donor 29	rectum
22	chr6:26160600-26163400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
23	chr6:26160600-26163400	Weak transcription	Left Ventricle	heart
24	chr6:26160600-26163600	Weak transcription	Brain Hippocampus Middle	brain
25	chr6:26160600-26163600	Weak transcription	Duodenum Mucosa	Duodenum
26	chr6:26160600-26164000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr6:26160600-26164000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr6:26160600-26164400	Weak transcription	Rectal Smooth Muscle	rectum
29	chr6:26160600-26165800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr6:26160600-26169400	Weak transcription	Fetal Kidney	kidney
31	chr6:26160600-26170200	Weak transcription	Hela-S3	cervix
32	chr6:26160600-26170400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr6:26160600-26170600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr6:26160600-26171200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr6:26160600-26171200	Weak transcription	HUES6 Cell Line	embryonic stem cell
36	chr6:26160600-26171200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
37	chr6:26160600-26171200	Weak transcription	Stomach Smooth Muscle	stomach
38	chr6:26160600-26171400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr6:26160600-26171400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr6:26160600-26171400	Weak transcription	Colon Smooth Muscle	Colon
41	chr6:26160600-26171400	Weak transcription	Psoas Muscle	Psoas
42	chr6:26160600-26171600	Weak transcription	H1 Cell Line	embryonic stem cell
43	chr6:26160600-26171600	Weak transcription	H9 Cell Line	embryonic stem cell
44	chr6:26160600-26171600	Weak transcription	Aorta	Aorta
45	chr6:26160600-26171600	Weak transcription	Brain Cingulate Gyrus	brain
46	chr6:26160600-26171600	Weak transcription	Brain Substantia Nigra	brain
47	chr6:26160600-26171800	Weak transcription	Placenta Amnion	Placenta Amnion
48	chr6:26160800-26163200	Enhancers	Fetal Brain Male	brain
49	chr6:26160800-26163400	Weak transcription	Primary hematopoietic stem cells	blood
50	chr6:26160800-26163800	Enhancers	Rectal Mucosa Donor 31	rectum

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