Variant report

Variant	rs10270137
Chromosome Location	chr7:33415985-33415986
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10230991	0.81[AFR][1000 genomes]
rs10235943	0.81[AFR][1000 genomes]
rs10236358	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs10243590	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs10245418	0.83[AFR][1000 genomes]
rs10250312	0.81[AFR][1000 genomes]
rs10252552	0.83[AFR][1000 genomes]
rs10252935	0.81[AFR][1000 genomes]
rs10253352	0.90[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs10253574	1.00[EUR][1000 genomes]
rs10257379	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs10259513	0.81[AFR][1000 genomes]
rs10259674	0.83[AFR][1000 genomes]
rs10266641	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs10272446	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs10276929	0.83[AFR][1000 genomes]
rs10951385	0.91[AFR][1000 genomes]
rs12112737	1.00[EUR][1000 genomes]
rs12333380	0.81[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12334131	0.81[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12669847	0.81[AFR][1000 genomes]
rs12672071	0.81[AFR][1000 genomes]
rs12672496	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	0.83[AFR][1000 genomes]
rs4298411	1.00[AFR][1000 genomes]
rs9785054	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 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

No data

Chromatin state (count:55 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:33355200-33419600	Weak transcription	Primary T cells from cord blood	blood
2	chr7:33384000-33425400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
3	chr7:33387000-33425200	Weak transcription	Primary T cells fromperipheralblood	blood
4	chr7:33389000-33437400	Weak transcription	Liver	Liver
5	chr7:33392600-33423000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr7:33393600-33419600	Weak transcription	Rectal Smooth Muscle	rectum
7	chr7:33394200-33419400	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr7:33394200-33419600	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr7:33394400-33427800	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr7:33396600-33420000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr7:33396600-33422000	Weak transcription	Small Intestine	intestine
12	chr7:33402600-33419600	Weak transcription	Brain Cingulate Gyrus	brain
13	chr7:33403000-33427400	Weak transcription	Primary T helper cells PMA-I stimulated	--
14	chr7:33403400-33437800	Weak transcription	Brain Substantia Nigra	brain
15	chr7:33403800-33419600	Weak transcription	Brain Angular Gyrus	brain
16	chr7:33403800-33430400	Weak transcription	Brain Hippocampus Middle	brain
17	chr7:33404000-33419800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr7:33404000-33433000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr7:33404600-33419600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr7:33404600-33419600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr7:33404800-33419600	Weak transcription	Right Ventricle	heart
22	chr7:33405200-33420000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr7:33405200-33421600	Weak transcription	Colon Smooth Muscle	Colon
24	chr7:33405400-33418400	Weak transcription	Fetal Muscle Leg	muscle
25	chr7:33405400-33422200	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr7:33405600-33419600	Weak transcription	Fetal Muscle Trunk	muscle
27	chr7:33405600-33423600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr7:33405800-33418400	Weak transcription	Aorta	Aorta
29	chr7:33405800-33419600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
30	chr7:33405800-33419600	Weak transcription	Stomach Smooth Muscle	stomach
31	chr7:33406000-33418200	Weak transcription	Ovary	ovary
32	chr7:33406000-33419400	Weak transcription	Left Ventricle	heart
33	chr7:33406000-33419600	Weak transcription	Brain Anterior Caudate	brain
34	chr7:33406000-33419600	Weak transcription	Duodenum Smooth Muscle	Duodenum
35	chr7:33406000-33419600	Weak transcription	Fetal Stomach	stomach
36	chr7:33406000-33419800	Weak transcription	Fetal Lung	lung
37	chr7:33406000-33425400	Weak transcription	Primary B cells from cord blood	blood
38	chr7:33406400-33425400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr7:33407000-33429600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
40	chr7:33407200-33419400	Weak transcription	Fetal Heart	heart
41	chr7:33408000-33418400	Weak transcription	Adipose Nuclei	Adipose
42	chr7:33408200-33418400	Weak transcription	Primary T helper cells fromperipheralblood	blood
43	chr7:33408200-33431000	Weak transcription	Primary hematopoietic stem cells	blood
44	chr7:33408200-33434600	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr7:33408600-33434400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr7:33411800-33431000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr7:33412000-33423800	Weak transcription	Stomach Mucosa	stomach
48	chr7:33412200-33433200	Weak transcription	Psoas Muscle	Psoas
49	chr7:33413400-33418400	Weak transcription	HUES6 Cell Line	embryonic stem cell
50	chr7:33413400-33424400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links