Variant report

Variant	rs11902907
Chromosome Location	chr2:173452347-173452348
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 101 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:96)

rs_ID	r²[population]
rs10048692	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10048707	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10048825	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10176813	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10178654	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10180021	0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10186869	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10197678	0.93[ASN][1000 genomes]
rs10199472	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10201129	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10202550	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10207262	0.80[ASN][1000 genomes]
rs10208151	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10210546	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10427189	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10427315	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11887454	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11890159	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11891127	1.00[ASN][1000 genomes]
rs11896032	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11896178	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11897165	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11897495	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11897582	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11898137	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11898890	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11901110	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11901586	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11902810	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11904366	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12693005	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12693007	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12990751	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13007707	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13008835	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13009291	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13010205	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13023751	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13024218	0.80[ASN][1000 genomes]
rs13024431	0.80[ASN][1000 genomes]
rs13032610	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13032692	0.80[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13385403	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13385644	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13386103	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13388338	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13392808	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13394924	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13401945	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs13401980	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13405998	0.80[ASN][1000 genomes]
rs13408780	0.80[ASN][1000 genomes]
rs13415156	0.80[ASN][1000 genomes]
rs13415174	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13417334	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13425344	0.80[ASN][1000 genomes]
rs1531151	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs16860696	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16860697	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17299956	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17702263	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1869922	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1982410	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2290564	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2599267	0.80[ASN][1000 genomes]
rs2606069	0.80[ASN][1000 genomes]
rs28537209	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3087500	0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34139806	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34611798	0.80[ASN][1000 genomes]
rs34707897	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34888332	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35086707	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs35156154	0.80[ASN][1000 genomes]
rs35665064	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35809888	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35880823	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35951155	1.00[ASN][1000 genomes]
rs35999155	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs36118221	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3613	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56953655	0.81[AMR][1000 genomes]
rs59004833	0.87[ASN][1000 genomes]
rs59104969	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62167823	0.80[EUR][1000 genomes]
rs62167832	0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs62169270	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62169301	0.80[ASN][1000 genomes]
rs66460331	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6723872	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6752257	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs70937080	0.93[ASN][1000 genomes]
rs7566884	0.93[ASN][1000 genomes]
rs7567092	0.93[ASN][1000 genomes]
rs836589	0.80[ASN][1000 genomes]
rs9287957	0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533927	chr2:173161637-173796894	Active TSS Enhancers Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
2	esv2760591	chr2:173396905-173719520	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv3035	chr2:173419058-173463901	Strong transcription Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
4	nsv875415	chr2:173444462-173501069	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv875416	chr2:173444462-173504674	Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:120 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:173421600-173453400	Weak transcription	Pancreas	Pancrea
2	chr2:173421800-173465200	Weak transcription	Small Intestine	intestine
3	chr2:173426200-173460600	Weak transcription	HSMMtube	muscle
4	chr2:173430600-173461600	Weak transcription	Right Ventricle	heart
5	chr2:173431400-173480600	Weak transcription	Gastric	stomach
6	chr2:173432000-173462400	Weak transcription	Colon Smooth Muscle	Colon
7	chr2:173439800-173458000	Weak transcription	NHDF-Ad	bronchial
8	chr2:173440200-173458200	Weak transcription	Osteobl	bone
9	chr2:173440200-173467600	Weak transcription	NH-A	brain
10	chr2:173443200-173454400	Strong transcription	HUES6 Cell Line	embryonic stem cell
11	chr2:173443200-173455200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr2:173443200-173472200	Strong transcription	Primary neutrophils fromperipheralblood	blood
13	chr2:173443800-173453600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr2:173443800-173463200	Weak transcription	A549	lung
15	chr2:173444000-173453200	Strong transcription	Dnd41	blood
16	chr2:173444000-173453400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr2:173444000-173456200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr2:173444000-173464000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr2:173444200-173452800	Weak transcription	NHEK	skin
20	chr2:173444200-173453600	Weak transcription	Esophagus	oesophagus
21	chr2:173444200-173455600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr2:173444200-173470400	Weak transcription	Psoas Muscle	Psoas
23	chr2:173444400-173480200	Strong transcription	HepG2	liver
24	chr2:173444600-173465400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
25	chr2:173445000-173453200	Strong transcription	HMEC	breast
26	chr2:173445000-173453400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr2:173445000-173455400	Strong transcription	Primary B cells from peripheral blood	blood
28	chr2:173445200-173463200	Weak transcription	Fetal Brain Female	brain
29	chr2:173445400-173452400	Strong transcription	HUES48 Cell Line	embryonic stem cell
30	chr2:173445400-173461000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
31	chr2:173445400-173462600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr2:173445400-173471000	Weak transcription	Brain Substantia Nigra	brain
33	chr2:173445600-173453000	Weak transcription	Brain Angular Gyrus	brain
34	chr2:173446000-173454000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr2:173446000-173454400	Strong transcription	HUES64 Cell Line	embryonic stem cell
36	chr2:173446400-173460400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr2:173447600-173453400	Weak transcription	Aorta	Aorta
38	chr2:173447800-173453400	Weak transcription	Brain Inferior Temporal Lobe	brain
39	chr2:173447800-173454000	Weak transcription	Placenta	Placenta
40	chr2:173447800-173460200	Weak transcription	HUVEC	blood vessel
41	chr2:173448000-173463400	Weak transcription	Stomach Mucosa	stomach
42	chr2:173448200-173459000	Weak transcription	Brain Germinal Matrix	brain
43	chr2:173448400-173452400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr2:173448800-173455800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
45	chr2:173449200-173453200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr2:173449400-173454600	Strong transcription	Primary monocytes fromperipheralblood	blood
47	chr2:173449400-173454600	Strong transcription	Duodenum Mucosa	Duodenum
48	chr2:173449400-173455400	Strong transcription	Fetal Thymus	thymus
49	chr2:173449400-173456200	Strong transcription	Fetal Intestine Small	intestine
50	chr2:173449400-173456400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood

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