Variant report

Variant	rs2208035
Chromosome Location	chr10:52274113-52274114
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:52273248..52274821-chr10:52291297..52292939,2	MCF-7	breast:
2	chr10:52272246..52274913-chr10:52277739..52279580,2	MCF-7	breast:
3	chr10:52272048..52276086-chr10:52381938..52384651,3	MCF-7	breast:
4	chr10:52271127..52273442-chr10:52273762..52275494,2	MCF-7	breast:
5	chr10:52271610..52273554-chr10:52274092..52276247,2	MCF-7	breast:
6	chr10:52260554..52263861-chr10:52272806..52275340,3	K562	blood:
7	chr10:52272629..52275165-chr10:52281578..52283752,2	K562	blood:

Variant related genes	Relation type
ENSG00000198964	Chromatin interaction

Extended variants
information (count: 62 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs1203374	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1203379	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1203383	0.91[CEU][hapmap];0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1203384	0.92[CEU][hapmap];0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1203391	0.91[CEU][hapmap];0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1203402	1.00[CEU][hapmap];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1203412	0.92[CEU][hapmap];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1203416	1.00[ASN][1000 genomes]
rs1203417	1.00[ASN][1000 genomes]
rs1203419	1.00[ASN][1000 genomes]
rs1203422	1.00[ASN][1000 genomes]
rs1203426	0.85[EUR][1000 genomes]
rs1203427	0.91[CEU][hapmap];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1209146	0.85[EUR][1000 genomes]
rs1211373	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2024871	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2064760	0.85[CEU][hapmap];0.94[EUR][1000 genomes]
rs2208037	0.94[YRI][hapmap]
rs2339508	1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs2339509	1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs2474611	1.00[ASN][1000 genomes]
rs2574945	1.00[ASN][1000 genomes]
rs2574976	1.00[ASN][1000 genomes]
rs2688874	1.00[ASN][1000 genomes]
rs2688876	1.00[ASN][1000 genomes]
rs2688883	1.00[ASN][1000 genomes]
rs2688884	1.00[ASN][1000 genomes]
rs2842099	1.00[ASN][1000 genomes]
rs2842110	1.00[ASN][1000 genomes]
rs2860490	0.93[YRI][hapmap]
rs2983346	0.94[EUR][1000 genomes]
rs2983348	1.00[CEU][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2983349	0.94[EUR][1000 genomes]
rs2983352	1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs2983358	1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs2983362	0.93[YRI][hapmap]
rs2983363	0.93[YRI][hapmap]
rs2983372	1.00[CEU][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3001855	0.81[YRI][hapmap]
rs3011711	0.93[YRI][hapmap]
rs3011712	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3011715	0.92[CEU][hapmap];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3011768	1.00[CEU][hapmap];0.93[YRI][hapmap];0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3011778	0.81[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs3011781	1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs3011795	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3011799	1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs7094723	0.82[CEU][hapmap];0.80[EUR][1000 genomes]
rs72801753	1.00[ASN][1000 genomes]
rs7923756	1.00[ASN][1000 genomes]
rs910818	0.86[CEU][hapmap];0.94[EUR][1000 genomes]
rs910819	0.91[CEU][hapmap];0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9416590	0.91[CEU][hapmap];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1054775	chr10:51595893-52392361	Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
2	nsv1051087	chr10:51886486-52447295	Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
3	nsv916214	chr10:51886486-52458983	Active TSS Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
4	nsv918212	chr10:51886486-52465482	Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
5	nsv817412	chr10:51911034-52432990	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS 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	31 gene(s)	inside rSNPs	diseases
6	nsv895391	chr10:52260398-52291608	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
7	nsv895392	chr10:52263910-52291608	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
8	nsv467193	chr10:52265265-52289664	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
9	nsv550855	chr10:52265265-52289664	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:83 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:52262200-52287200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr10:52266800-52282400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr10:52267000-52282400	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr10:52267600-52277800	Enhancers	Brain Anterior Caudate	brain
5	chr10:52268200-52282400	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr10:52268200-52282600	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr10:52268400-52282200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr10:52268800-52278800	Weak transcription	Primary B cells from cord blood	blood
9	chr10:52270000-52282400	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr10:52270000-52282800	Weak transcription	Monocytes-CD14+_RO01746	blood
11	chr10:52270200-52282600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr10:52271200-52274600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr10:52271200-52274600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr10:52271200-52283000	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr10:52271600-52276800	Weak transcription	Fetal Lung	lung
16	chr10:52271600-52277400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr10:52271600-52300600	Weak transcription	Aorta	Aorta
18	chr10:52271800-52274800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr10:52271800-52280800	Weak transcription	Primary monocytes fromperipheralblood	blood
20	chr10:52272200-52281000	Weak transcription	Fetal Intestine Large	intestine
21	chr10:52272400-52275600	Weak transcription	Fetal Heart	heart
22	chr10:52272400-52280000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
23	chr10:52272400-52280400	Weak transcription	Rectal Mucosa Donor 31	rectum
24	chr10:52272400-52284600	Weak transcription	Stomach Smooth Muscle	stomach
25	chr10:52272600-52302800	Weak transcription	Fetal Stomach	stomach
26	chr10:52272800-52274400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
27	chr10:52272800-52274600	Weak transcription	Liver	Liver
28	chr10:52272800-52274600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
29	chr10:52272800-52274600	Weak transcription	Right Atrium	heart
30	chr10:52272800-52275000	Weak transcription	Psoas Muscle	Psoas
31	chr10:52272800-52275200	Weak transcription	Esophagus	oesophagus
32	chr10:52272800-52275800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr10:52272800-52276000	Weak transcription	Duodenum Smooth Muscle	Duodenum
34	chr10:52272800-52279000	Weak transcription	Fetal Intestine Small	intestine
35	chr10:52272800-52281200	Weak transcription	Ovary	ovary
36	chr10:52272800-52281400	Weak transcription	Placenta	Placenta
37	chr10:52272800-52281600	Weak transcription	HepG2	liver
38	chr10:52272800-52288200	Weak transcription	HSMMtube	muscle
39	chr10:52273000-52275000	Enhancers	HMEC	breast
40	chr10:52273000-52275200	Enhancers	NHEK	skin
41	chr10:52273000-52275800	Weak transcription	Pancreatic Islets	Pancreatic Islet
42	chr10:52273200-52274200	Weak transcription	Brain Angular Gyrus	brain
43	chr10:52273200-52274600	Weak transcription	Pancreas	Pancrea
44	chr10:52273200-52274800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
45	chr10:52273200-52275200	Weak transcription	Gastric	stomach
46	chr10:52273200-52278200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
47	chr10:52273200-52278600	Weak transcription	Primary hematopoietic stem cells	blood
48	chr10:52273200-52279000	Weak transcription	Lung	lung
49	chr10:52273200-52281000	Weak transcription	Fetal Muscle Trunk	muscle
50	chr10:52273200-52281600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links