Variant report

Variant	rs7317464
Chromosome Location	chr13:110491970-110491971
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1023305	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1023306	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12184672	1.00[EUR][1000 genomes]
rs1335612	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1335613	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1967912	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7317502	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7317716	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7331580	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7332843	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7358854	0.89[AFR][1000 genomes]
rs7358932	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7358936	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7358951	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73608783	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7982658	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7983073	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7984046	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7986269	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7986378	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7986897	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7989371	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7990525	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7997262	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7999146	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8002388	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9301413	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9583429	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9583430	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9583431	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9587996	1.00[EUR][1000 genomes]
rs9587999	1.00[EUR][1000 genomes]
rs9588000	1.00[EUR][1000 genomes]
rs9588001	1.00[AMR][1000 genomes]
rs9588002	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9588003	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9588004	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9588005	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9588007	1.00[EUR][1000 genomes]

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:110488400-110496200	Weak transcription	Aorta	Aorta
2	chr13:110489600-110492600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr13:110489600-110497200	Weak transcription	Stomach Mucosa	stomach
4	chr13:110489800-110492000	Weak transcription	Dnd41	blood
5	chr13:110489800-110492600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr13:110489800-110492600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr13:110489800-110492600	Weak transcription	Pancreas	Pancrea
8	chr13:110489800-110492800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr13:110490800-110492400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr13:110491000-110492600	Enhancers	Muscle Satellite Cultured Cells	--
11	chr13:110491000-110494800	Enhancers	HSMM	muscle
12	chr13:110491600-110492600	Enhancers	Primary hematopoietic stem cells	blood
13	chr13:110491600-110492600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr13:110491600-110493600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr13:110491600-110493800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr13:110491800-110492200	Weak transcription	HSMMtube	muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links