Variant report

Variant	rs9467694
Chromosome Location	chr6:26257694-26257695
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs10046345	1.00[AMR][1000 genomes]
rs10214495	0.81[AFR][1000 genomes]
rs9467693	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]

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	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	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
16	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

No data

Chromatin state (count:49 , 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	chr6:26253800-26258400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr6:26253800-26260600	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr6:26253800-26265400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr6:26253800-26271000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr6:26254000-26259800	Weak transcription	Fetal Kidney	kidney
7	chr6:26254000-26261800	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr6:26254200-26258200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr6:26254200-26258400	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr6:26254200-26258400	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr6:26254200-26258400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr6:26254200-26258800	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr6:26254200-26269200	Weak transcription	Fetal Stomach	stomach
14	chr6:26254600-26258400	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr6:26254600-26260000	Weak transcription	Placenta	Placenta
16	chr6:26255000-26269400	Weak transcription	Primary hematopoietic stem cells	blood
17	chr6:26255400-26257800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr6:26255400-26258400	Weak transcription	Duodenum Smooth Muscle	Duodenum
19	chr6:26255400-26260400	Weak transcription	Primary neutrophils fromperipheralblood	blood
20	chr6:26255600-26258400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr6:26255600-26270400	Weak transcription	Primary B cells from cord blood	blood
22	chr6:26255600-26270400	Weak transcription	Primary T cells from cord blood	blood
23	chr6:26255800-26269400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr6:26256200-26258600	Strong transcription	Thymus	Thymus
25	chr6:26257000-26258000	Enhancers	Rectal Mucosa Donor 31	rectum
26	chr6:26257000-26258000	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr6:26257000-26258800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr6:26257200-26257800	Enhancers	Fetal Intestine Small	intestine
29	chr6:26257200-26259000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr6:26257200-26259000	Enhancers	Stomach Mucosa	stomach
31	chr6:26257200-26260600	Active TSS	Duodenum Mucosa	Duodenum
32	chr6:26257400-26257800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr6:26257400-26257800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr6:26257400-26257800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr6:26257400-26258000	Enhancers	Primary monocytes fromperipheralblood	blood
36	chr6:26257400-26258000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr6:26257400-26258200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
38	chr6:26257400-26258600	Enhancers	GM12878-XiMat	blood
39	chr6:26257400-26259200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr6:26257400-26259200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr6:26257400-26259200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr6:26257400-26259200	Flanking Active TSS	HepG2	liver
43	chr6:26257400-26259600	Active TSS	Fetal Intestine Large	intestine
44	chr6:26257600-26257800	Enhancers	Gastric	stomach
45	chr6:26257600-26258000	Enhancers	Rectal Mucosa Donor 29	rectum
46	chr6:26257600-26258200	Weak transcription	Brain Germinal Matrix	brain
47	chr6:26257600-26259200	Enhancers	Cortex derived primary cultured neurospheres	brain
48	chr6:26257600-26259800	Weak transcription	Fetal Thymus	thymus
49	chr6:26257600-26261000	Weak transcription	K562	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links