Variant report

Variant	rs9810059
Chromosome Location	chr3:113100734-113100735
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs13326562	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs13327031	1.00[EUR][1000 genomes]
rs13353449	1.00[EUR][1000 genomes]
rs16860734	1.00[CEU][hapmap]
rs2399487	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28539944	0.81[EUR][1000 genomes]
rs3995908	1.00[CEU][hapmap];1.00[GIH][hapmap];0.87[TSI][hapmap]
rs4419353	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6438134	1.00[CEU][hapmap]
rs6438154	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6763234	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6779241	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs6780720	1.00[CEU][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6781507	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6808103	1.00[CEU][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72950895	0.81[EUR][1000 genomes]
rs7612448	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs7618195	0.86[EUR][1000 genomes]
rs7625829	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];0.95[EUR][1000 genomes]
rs7629636	1.00[CEU][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7645188	1.00[CEU][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7652801	1.00[CEU][hapmap];1.00[GIH][hapmap]
rs9810754	1.00[GIH][hapmap];1.00[TSI][hapmap];0.81[EUR][1000 genomes]
rs9811168	0.90[EUR][1000 genomes]
rs9820386	0.83[LWK][hapmap]
rs9820627	1.00[CEU][hapmap]
rs9823770	1.00[CEU][hapmap]
rs9827772	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];0.86[EUR][1000 genomes]
rs9836199	0.90[EUR][1000 genomes]
rs9851183	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];0.82[LWK][hapmap];1.00[MEX][hapmap];0.95[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9851407	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9852068	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs9853439	1.00[CEU][hapmap]
rs9860473	0.95[EUR][1000 genomes]
rs9863114	0.90[EUR][1000 genomes]
rs9878186	1.00[CEU][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3431441	chr3:112453467-113213252	Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
2	nsv1013506	chr3:112890608-113680951	Weak transcription Bivalent/Poised TSS Enhancers Strong transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	51 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:53 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:113042200-113116800	Weak transcription	Primary B cells from cord blood	blood
2	chr3:113042400-113103600	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr3:113066200-113102800	Weak transcription	Aorta	Aorta
4	chr3:113066400-113117600	Weak transcription	Fetal Muscle Leg	muscle
5	chr3:113068400-113117000	Weak transcription	Thymus	Thymus
6	chr3:113069000-113101800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr3:113072400-113117200	Weak transcription	Primary T cells fromperipheralblood	blood
8	chr3:113074400-113184400	Weak transcription	Hela-S3	cervix
9	chr3:113077800-113102400	Weak transcription	HSMM	muscle
10	chr3:113078600-113109800	Weak transcription	Fetal Muscle Trunk	muscle
11	chr3:113080000-113114200	Weak transcription	Primary T helper cells fromperipheralblood	blood
12	chr3:113080000-113123800	Weak transcription	Primary B cells from peripheral blood	blood
13	chr3:113080200-113117600	Weak transcription	Psoas Muscle	Psoas
14	chr3:113080800-113143800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr3:113081600-113103400	Weak transcription	Duodenum Mucosa	Duodenum
16	chr3:113081600-113104400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr3:113081600-113105600	Weak transcription	Esophagus	oesophagus
18	chr3:113081600-113105800	Weak transcription	Gastric	stomach
19	chr3:113081600-113106200	Weak transcription	Lung	lung
20	chr3:113081600-113121200	Weak transcription	Ovary	ovary
21	chr3:113081600-113121200	Weak transcription	Pancreas	Pancrea
22	chr3:113081800-113116600	Weak transcription	Stomach Smooth Muscle	stomach
23	chr3:113082200-113113200	Weak transcription	Rectal Mucosa Donor 31	rectum
24	chr3:113086200-113105800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr3:113086200-113106400	Weak transcription	Fetal Stomach	stomach
26	chr3:113090800-113106600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr3:113090800-113121200	Weak transcription	Rectal Mucosa Donor 29	rectum
28	chr3:113091800-113104600	Weak transcription	NH-A	brain
29	chr3:113092400-113134200	Weak transcription	Fetal Kidney	kidney
30	chr3:113093600-113134800	Weak transcription	Primary T helper cells PMA-I stimulated	--
31	chr3:113094200-113108800	Weak transcription	Brain Hippocampus Middle	brain
32	chr3:113096200-113105600	Weak transcription	Liver	Liver
33	chr3:113096400-113106600	Weak transcription	GM12878-XiMat	blood
34	chr3:113096600-113121200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr3:113097400-113101800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
36	chr3:113097600-113103600	Weak transcription	Primary T cells from cord blood	blood
37	chr3:113097800-113101000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr3:113097800-113105800	Weak transcription	Fetal Intestine Large	intestine
39	chr3:113097800-113117800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr3:113098200-113117000	Weak transcription	Skeletal Muscle Female	skeletal muscle
41	chr3:113098800-113134800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
42	chr3:113099000-113104000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
43	chr3:113099000-113134800	Weak transcription	A549	lung
44	chr3:113099400-113106800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
45	chr3:113099400-113113400	Weak transcription	Left Ventricle	heart
46	chr3:113099600-113144800	Weak transcription	Rectal Smooth Muscle	rectum
47	chr3:113099800-113102000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr3:113099800-113103400	Weak transcription	Adipose Nuclei	Adipose
49	chr3:113099800-113106200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr3:113099800-113106800	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