Variant report

Variant	rs4362200
Chromosome Location	chr12:45054054-45054055
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 79 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:76)

rs_ID	r²[population]
rs10506253	0.91[JPT][hapmap];1.00[YRI][hapmap]
rs10506254	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10506255	1.00[CHB][hapmap];1.00[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.86[TSI][hapmap];0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10785516	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10880662	0.83[ASN][1000 genomes]
rs11182607	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11182608	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11182617	1.00[ASW][hapmap];0.85[CHD][hapmap];0.86[TSI][hapmap];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11182633	0.82[CHD][hapmap]
rs11609932	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11615822	0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12578861	0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12579312	0.82[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs12580824	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.86[TSI][hapmap];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12581256	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12812313	0.82[AFR][1000 genomes]
rs12812412	0.84[JPT][hapmap]
rs12817968	0.93[AFR][1000 genomes]
rs12818520	0.84[CHD][hapmap];0.84[JPT][hapmap];0.88[LWK][hapmap]
rs12820225	0.93[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs12825403	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12827088	0.82[JPT][hapmap]
rs12827992	1.00[CHB][hapmap];0.92[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.94[LWK][hapmap];0.85[MEX][hapmap];0.83[MKK][hapmap];0.86[TSI][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12828039	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12830054	0.82[AFR][1000 genomes]
rs12830788	1.00[CHB][hapmap];0.92[JPT][hapmap];0.82[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs1450538	1.00[CHB][hapmap];1.00[CHD][hapmap];0.83[TSI][hapmap];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1452259	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1452260	1.00[CHB][hapmap];1.00[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.86[TSI][hapmap];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1452261	1.00[CHB][hapmap];0.88[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.86[TSI][hapmap];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1517205	0.92[CHB][hapmap];1.00[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.85[MEX][hapmap];0.83[MKK][hapmap];0.86[TSI][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1562965	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1597808	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs17571851	0.92[JPT][hapmap];1.00[YRI][hapmap]
rs17572194	0.92[JPT][hapmap];1.00[YRI][hapmap]
rs17573326	0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17573382	0.92[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17575124	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs17575145	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs17651444	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17651576	0.86[EUR][1000 genomes]
rs17652016	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17652045	1.00[CHB][hapmap];1.00[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.86[TSI][hapmap];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17652213	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17652890	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1869161	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2122530	1.00[CHB][hapmap];1.00[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.86[TSI][hapmap];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2290353	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2290354	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2290355	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs33995718	0.86[EUR][1000 genomes]
rs34059115	0.82[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs34354933	0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs34500282	0.89[AFR][1000 genomes]
rs34560815	0.96[AFR][1000 genomes];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34882841	0.96[AFR][1000 genomes];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34985115	0.82[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs35051815	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35180883	0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs35889925	0.93[AFR][1000 genomes]
rs35934410	0.84[EUR][1000 genomes]
rs35977363	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36054479	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55841784	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs55996511	0.96[ASN][1000 genomes]
rs57004692	0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs57933837	0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs59379685	0.81[EUR][1000 genomes]
rs61932363	0.93[AFR][1000 genomes]
rs61932405	0.96[AFR][1000 genomes];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs66572050	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7295695	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7308333	0.84[EUR][1000 genomes]
rs7971322	0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7971937	0.82[AFR][1000 genomes]
rs7978549	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1049818	chr12:44486312-45133783	Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	esv3378050	chr12:44963059-45264289	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	1 gene(s)	inside rSNPs	diseases
3	nsv430506	chr12:45003342-45072343	Enhancers Genic enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:45023400-45055600	Weak transcription	Primary T helper cells PMA-I stimulated	--
2	chr12:45031600-45059200	Weak transcription	Primary T helper cells fromperipheralblood	blood
3	chr12:45044400-45062800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
4	chr12:45049400-45069000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr12:45050400-45061200	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr12:45050800-45054200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr12:45050800-45060000	Weak transcription	Fetal Brain Female	brain
8	chr12:45051800-45081200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
9	chr12:45053600-45055200	Strong transcription	Primary T killer naive cells fromperipheralblood	blood
10	chr12:45053800-45054800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr12:45054000-45054400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr12:45054000-45055600	Strong transcription	Primary T cells fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links