Variant report

Variant	rs10266641
Chromosome Location	chr7:33404827-33404828
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10230991	1.00[YRI][hapmap];0.81[AFR][1000 genomes]
rs10235943	1.00[YRI][hapmap];0.81[AFR][1000 genomes]
rs10236358	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs10239609	1.00[YRI][hapmap]
rs10243590	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs10245418	1.00[YRI][hapmap];0.83[AFR][1000 genomes]
rs10250312	1.00[YRI][hapmap];0.81[AFR][1000 genomes]
rs10252552	1.00[YRI][hapmap];0.83[AFR][1000 genomes]
rs10252927	1.00[YRI][hapmap]
rs10252935	1.00[YRI][hapmap];0.81[AFR][1000 genomes]
rs10253352	1.00[YRI][hapmap];0.90[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs10253574	1.00[YRI][hapmap];1.00[EUR][1000 genomes]
rs10257379	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs10259513	1.00[YRI][hapmap];0.81[AFR][1000 genomes]
rs10259674	1.00[YRI][hapmap];0.83[AFR][1000 genomes]
rs10267370	1.00[YRI][hapmap]
rs10270137	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs10272446	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs10276929	1.00[YRI][hapmap];0.83[AFR][1000 genomes]
rs10951385	1.00[YRI][hapmap];0.91[AFR][1000 genomes]
rs12112737	1.00[EUR][1000 genomes]
rs12333380	1.00[YRI][hapmap];0.81[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12334131	1.00[YRI][hapmap];0.81[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12669847	0.81[AFR][1000 genomes]
rs12672071	1.00[YRI][hapmap];0.81[AFR][1000 genomes]
rs12672496	1.00[YRI][hapmap];0.83[AFR][1000 genomes]
rs28465518	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs28478218	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs28564487	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs28622379	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs28673971	0.81[AFR][1000 genomes]
rs3779240	1.00[YRI][hapmap];0.83[AFR][1000 genomes]
rs4298411	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs6969260	1.00[YRI][hapmap]
rs6974593	1.00[YRI][hapmap]
rs9785054	1.00[YRI][hapmap];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv606610	chr7:33218763-33486316	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1016416	chr7:33241443-33559477	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv916660	chr7:33272493-33506384	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv830944	chr7:33389892-33549882	Weak transcription Strong transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv511958	chr7:33402220-33405040	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
6	esv3353498	chr7:33402877-33404875	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:42 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:33355200-33419600	Weak transcription	Primary T cells from cord blood	blood
2	chr7:33381400-33407200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr7:33384000-33425400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
4	chr7:33385800-33407000	Weak transcription	Primary T helper cells fromperipheralblood	blood
5	chr7:33386000-33407400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr7:33386400-33408200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr7:33387000-33425200	Weak transcription	Primary T cells fromperipheralblood	blood
8	chr7:33389000-33437400	Weak transcription	Liver	Liver
9	chr7:33391600-33407400	Weak transcription	Primary hematopoietic stem cells	blood
10	chr7:33392600-33423000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
11	chr7:33393600-33419600	Weak transcription	Rectal Smooth Muscle	rectum
12	chr7:33394200-33419400	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr7:33394200-33419600	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr7:33394400-33427800	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr7:33395000-33407400	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr7:33395400-33405000	Weak transcription	HUES6 Cell Line	embryonic stem cell
17	chr7:33396600-33420000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr7:33396600-33422000	Weak transcription	Small Intestine	intestine
19	chr7:33402600-33419600	Weak transcription	Brain Cingulate Gyrus	brain
20	chr7:33403000-33427400	Weak transcription	Primary T helper cells PMA-I stimulated	--
21	chr7:33403400-33405000	Weak transcription	Brain Anterior Caudate	brain
22	chr7:33403400-33437800	Weak transcription	Brain Substantia Nigra	brain
23	chr7:33403800-33419600	Weak transcription	Brain Angular Gyrus	brain
24	chr7:33403800-33430400	Weak transcription	Brain Hippocampus Middle	brain
25	chr7:33404000-33419800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr7:33404000-33433000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
27	chr7:33404200-33407400	Weak transcription	Fetal Brain Male	brain
28	chr7:33404400-33405200	ZNF genes & repeats	Aorta	Aorta
29	chr7:33404400-33405200	ZNF genes & repeats	Colon Smooth Muscle	Colon
30	chr7:33404400-33405200	Strong transcription	Ovary	ovary
31	chr7:33404400-33405400	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
32	chr7:33404400-33406000	ZNF genes & repeats	Fetal Stomach	stomach
33	chr7:33404600-33419600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr7:33404600-33419600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr7:33404800-33405000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr7:33404800-33405400	ZNF genes & repeats	Fetal Muscle Leg	muscle
37	chr7:33404800-33405400	ZNF genes & repeats	Left Ventricle	heart
38	chr7:33404800-33405400	ZNF genes & repeats	Lung	lung
39	chr7:33404800-33405800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr7:33404800-33405800	Strong transcription	Stomach Smooth Muscle	stomach
41	chr7:33404800-33406000	ZNF genes & repeats	Fetal Lung	lung
42	chr7:33404800-33419600	Weak transcription	Right Ventricle	heart

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