Variant report

Variant	rs3800615
Chromosome Location	chr7:137314835-137314836
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:137311964..137313853-chr7:137313862..137316637,2	K562	blood:

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs10155828	1.00[JPT][hapmap]
rs10155832	1.00[JPT][hapmap]
rs10155936	1.00[JPT][hapmap]
rs10156007	1.00[JPT][hapmap]
rs10156042	1.00[JPT][hapmap]
rs10273400	1.00[JPT][hapmap]
rs10275097	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs11971016	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs11971088	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs11975858	1.00[JPT][hapmap]
rs11978263	1.00[JPT][hapmap]
rs11982810	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1424367	1.00[JPT][hapmap]
rs2037677	1.00[JPT][hapmap]
rs2037678	1.00[JPT][hapmap]
rs28787723	0.81[ASN][1000 genomes]
rs3778784	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs3778786	0.81[ASN][1000 genomes]
rs3778787	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs3778789	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs3778792	1.00[JPT][hapmap]
rs3800616	1.00[JPT][hapmap]
rs3800617	1.00[JPT][hapmap]
rs3800618	1.00[JPT][hapmap]
rs3800620	1.00[JPT][hapmap]
rs3800621	1.00[JPT][hapmap]
rs3823550	1.00[JPT][hapmap]
rs58245080	0.81[ASN][1000 genomes]
rs58503212	0.87[ASN][1000 genomes]
rs59626548	0.81[ASN][1000 genomes]
rs59811187	0.81[ASN][1000 genomes]
rs6467712	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs6467713	1.00[JPT][hapmap]
rs6946782	1.00[JPT][hapmap]
rs6946901	1.00[JPT][hapmap]
rs6947070	1.00[JPT][hapmap]
rs6947756	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs6957431	1.00[JPT][hapmap]
rs6967488	1.00[CHB][hapmap];1.00[EUR][1000 genomes]
rs6979919	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs73461023	0.90[ASN][1000 genomes]
rs73461041	0.81[ASN][1000 genomes]
rs73461053	0.81[ASN][1000 genomes]
rs73461054	0.81[ASN][1000 genomes]
rs73461063	0.81[ASN][1000 genomes]
rs7786978	1.00[JPT][hapmap]
rs7787201	1.00[JPT][hapmap]
rs7788632	0.86[JPT][hapmap];0.81[ASN][1000 genomes]
rs7789901	1.00[JPT][hapmap]
rs7797692	1.00[JPT][hapmap]
rs7801047	1.00[JPT][hapmap]

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	nsv869820	chr7:136990386-137347718	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv1022793	chr7:137187383-137619359	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	esv1812888	chr7:137283212-137366467	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:137277200-137326800	Weak transcription	Osteobl	bone
2	chr7:137277600-137315400	Weak transcription	NH-A	brain
3	chr7:137282800-137337400	Weak transcription	HSMMtube	muscle
4	chr7:137294000-137328400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr7:137297600-137324200	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr7:137304600-137319200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr7:137304800-137320000	Weak transcription	Aorta	Aorta
8	chr7:137313200-137328400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr7:137313600-137321800	Weak transcription	Brain Germinal Matrix	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links