Variant report

Variant	rs2929275
Chromosome Location	chr15:44258897-44258898
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:44257421..44260379-chr15:44264658..44267581,2	K562	blood:
2	chr15:44257377..44260472-chr15:44263670..44267581,4	K562	blood:

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs11853395	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs12437804	0.81[GIH][hapmap];0.81[TSI][hapmap]
rs1426658	0.92[GIH][hapmap];0.81[TSI][hapmap]
rs1561458	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs16948098	1.00[CEU][hapmap]
rs16949992	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs1820482	0.85[GIH][hapmap];0.81[TSI][hapmap]
rs2412853	0.92[GIH][hapmap];0.81[TSI][hapmap]
rs2412854	0.92[GIH][hapmap];0.81[TSI][hapmap]
rs2615297	0.85[GIH][hapmap]
rs2623015	0.97[EUR][1000 genomes]
rs2733221	0.84[GIH][hapmap]
rs28654093	0.83[EUR][1000 genomes]
rs28729677	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2918952	1.00[CEU][hapmap];1.00[TSI][hapmap];0.83[EUR][1000 genomes]
rs2929277	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2929279	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs2929282	0.97[EUR][1000 genomes]
rs2930523	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs2930524	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs2930525	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34497759	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4270152	1.00[CEU][hapmap];0.93[TSI][hapmap]
rs4321171	0.83[EUR][1000 genomes]
rs481837	1.00[CEU][hapmap];0.93[TSI][hapmap]
rs483800	1.00[CEU][hapmap];0.86[TSI][hapmap]
rs4924729	0.92[GIH][hapmap]
rs492571	1.00[CEU][hapmap];1.00[TSI][hapmap];0.83[EUR][1000 genomes]
rs545119	0.86[EUR][1000 genomes]
rs59561000	0.86[EUR][1000 genomes]
rs59770554	0.86[EUR][1000 genomes]
rs6493094	0.92[GIH][hapmap];0.81[TSI][hapmap]
rs74009159	0.83[EUR][1000 genomes]
rs74009160	0.83[EUR][1000 genomes]
rs8033233	0.92[GIH][hapmap];0.81[TSI][hapmap]
rs8035382	1.00[CEU][hapmap];0.92[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.97[EUR][1000 genomes]
rs8035402	1.00[CEU][hapmap];0.92[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.97[EUR][1000 genomes]
rs8035689	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs8038096	0.81[TSI][hapmap]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1037786	chr15:43888926-44318587	Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
2	nsv542370	chr15:43888926-44318587	Weak transcription Genic enhancers Flanking Active TSS Active TSS Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
3	nsv431387	chr15:43929378-44862930	Weak transcription Strong transcription Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	158 gene(s)	inside rSNPs	diseases
4	nsv931051	chr15:43988761-44833518	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	154 gene(s)	inside rSNPs	diseases
5	nsv1044435	chr15:44176103-44507403	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
6	nsv977844	chr15:44251952-44264610	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:44251000-44267000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr15:44251600-44260400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr15:44251800-44259000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr15:44252000-44260400	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr15:44252000-44262000	Weak transcription	Fetal Brain Female	brain
6	chr15:44257400-44261800	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr15:44257400-44281000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr15:44258400-44263200	Enhancers	Brain Substantia Nigra	brain
9	chr15:44258600-44259000	Enhancers	Brain Cingulate Gyrus	brain
10	chr15:44258600-44259200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr15:44258600-44259200	Enhancers	Brain Angular Gyrus	brain
12	chr15:44258600-44259400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr15:44258600-44263000	Enhancers	Brain Hippocampus Middle	brain
14	chr15:44258800-44259000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr15:44258800-44259200	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr15:44258800-44259200	Enhancers	Muscle Satellite Cultured Cells	--
17	chr15:44258800-44259200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr15:44258800-44259200	Enhancers	NHDF-Ad	bronchial
19	chr15:44258800-44259400	Enhancers	Osteobl	bone
20	chr15:44258800-44260800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr15:44258800-44263200	Enhancers	Brain Anterior Caudate	brain

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