Variant report

Variant	rs4378566
Chromosome Location	chr15:45188662-45188663
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 86 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:61)

rs_ID	r²[population]
rs11070436	0.90[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs11543459	0.92[ASN][1000 genomes]
rs11630472	0.94[ASN][1000 genomes]
rs11636558	0.95[CHB][hapmap];0.87[JPT][hapmap];0.88[ASN][1000 genomes]
rs11639242	0.82[ASN][1000 genomes]
rs12050574	0.82[ASN][1000 genomes]
rs12050579	0.90[AFR][1000 genomes];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12050791	0.86[ASN][1000 genomes]
rs12592076	0.83[ASN][1000 genomes]
rs12592596	0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12593164	0.82[ASN][1000 genomes]
rs12593203	0.84[ASN][1000 genomes]
rs12593337	0.83[ASN][1000 genomes]
rs12595073	0.90[ASN][1000 genomes]
rs12595326	1.00[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.85[ASN][1000 genomes]
rs12595603	0.90[ASN][1000 genomes]
rs1288098	0.82[ASN][1000 genomes]
rs1288103	0.84[ASN][1000 genomes]
rs1288105	0.84[ASN][1000 genomes]
rs1290485	0.84[ASN][1000 genomes]
rs16975717	1.00[CEU][hapmap];0.90[JPT][hapmap];0.84[ASN][1000 genomes]
rs16975906	0.90[ASN][1000 genomes]
rs1704792	0.91[CHB][hapmap];0.87[JPT][hapmap]
rs1877029	0.89[ASN][1000 genomes]
rs2257231	0.80[ASN][1000 genomes]
rs2468044	0.81[ASN][1000 genomes]
rs2470906	0.85[ASN][1000 genomes]
rs28497325	0.83[ASN][1000 genomes]
rs28537968	0.84[ASN][1000 genomes]
rs28574953	0.88[ASN][1000 genomes]
rs28649153	0.87[ASN][1000 genomes]
rs2899129	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2948905	0.84[ASN][1000 genomes]
rs2948906	0.85[ASN][1000 genomes]
rs3110656	0.82[ASN][1000 genomes]
rs3110661	0.88[ASN][1000 genomes]
rs34561910	0.95[ASN][1000 genomes]
rs3858897	0.88[ASN][1000 genomes]
rs4082812	0.92[ASN][1000 genomes]
rs4520786	0.92[ASN][1000 genomes]
rs4635283	0.94[ASN][1000 genomes]
rs4774362	0.83[ASN][1000 genomes]
rs4775268	0.94[ASN][1000 genomes]
rs4775279	0.94[ASN][1000 genomes]
rs55956830	0.92[ASN][1000 genomes]
rs67440818	0.94[ASN][1000 genomes]
rs7162016	0.89[ASN][1000 genomes]
rs7162958	0.94[ASN][1000 genomes]
rs7163111	0.87[CHB][hapmap];0.83[JPT][hapmap];0.81[ASN][1000 genomes]
rs7163276	0.89[ASN][1000 genomes]
rs7165296	1.00[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap]
rs7165793	0.82[ASN][1000 genomes]
rs7175998	0.84[ASN][1000 genomes]
rs7183695	0.87[ASN][1000 genomes]
rs735480	0.80[ASN][1000 genomes]
rs74009451	0.86[ASN][1000 genomes]
rs8026050	0.86[ASN][1000 genomes]
rs8026423	0.84[ASN][1000 genomes]
rs8027024	0.85[ASN][1000 genomes]
rs8030847	0.82[ASN][1000 genomes]
rs8040024	0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:25 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758380	chr15:44968868-45422842	Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	95 gene(s)	inside rSNPs	diseases
2	esv2760029	chr15:44968868-45422842	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	95 gene(s)	inside rSNPs	diseases
3	nsv916374	chr15:45058112-45769052	Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	104 gene(s)	inside rSNPs	diseases
4	nsv1048668	chr15:45094019-45284278	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
5	nsv1050650	chr15:45096539-45229584	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	nsv1048867	chr15:45100852-45289756	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
7	esv2757599	chr15:45100852-45383620	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
8	nsv1036204	chr15:45105374-45284278	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
9	nsv1047353	chr15:45105374-45289756	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
10	nsv1040940	chr15:45105374-45300844	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
11	esv2753133	chr15:45105876-45268182	Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
12	esv34494	chr15:45105876-45268208	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
13	nsv1041613	chr15:45111367-45284278	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
14	nsv1053041	chr15:45117399-45289756	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
15	nsv1040140	chr15:45121635-45289756	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
16	nsv904181	chr15:45127793-45216343	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
17	nsv976929	chr15:45136882-45199085	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
18	nsv904182	chr15:45146708-45267670	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
19	nsv904183	chr15:45146708-45279246	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
20	nsv1050674	chr15:45152371-45250017	Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
21	nsv1037190	chr15:45152371-45259624	Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
22	nsv1053492	chr15:45152371-45275226	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
23	nsv1054418	chr15:45152371-45289756	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
24	nsv1037941	chr15:45152371-45296101	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
25	nsv1048317	chr15:45152371-45326205	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:45187800-45188800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
2	chr15:45187800-45189000	Enhancers	Primary T helper naive cells from peripheral blood	blood
3	chr15:45187800-45189000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
4	chr15:45188000-45189400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
5	chr15:45188200-45188800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
6	chr15:45188400-45188800	Enhancers	Primary B cells from peripheral blood	blood
7	chr15:45188600-45188800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr15:45188600-45188800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr15:45188600-45188800	Enhancers	Gastric	stomach
10	chr15:45188600-45189000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
11	chr15:45188600-45189000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood

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