Variant report

Variant	rs1605848
Chromosome Location	chr5:42427980-42427981
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 77 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:73)

rs_ID	r²[population]
rs10061299	1.00[CEU][hapmap]
rs10755268	0.93[EUR][1000 genomes]
rs1117110	0.85[EUR][1000 genomes]
rs11738365	0.89[CEU][hapmap];0.84[EUR][1000 genomes]
rs11742495	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11747975	0.88[CEU][hapmap];0.90[YRI][hapmap];0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11748366	0.82[EUR][1000 genomes]
rs11957616	0.81[EUR][1000 genomes]
rs13162973	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1396768	0.88[EUR][1000 genomes]
rs1396773	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1467049	0.89[CEU][hapmap];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1509452	0.80[CEU][hapmap];0.82[EUR][1000 genomes]
rs1509455	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs1509456	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs1567374	0.93[EUR][1000 genomes]
rs1605851	0.85[EUR][1000 genomes]
rs1858136	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs1858137	0.93[EUR][1000 genomes]
rs1858139	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1876788	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1876790	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs1912107	1.00[CEU][hapmap];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1960498	0.89[CEU][hapmap];0.85[EUR][1000 genomes]
rs2036745	0.89[CEU][hapmap];0.83[EUR][1000 genomes]
rs2175126	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2202883	0.84[EUR][1000 genomes]
rs2221712	0.84[EUR][1000 genomes]
rs2395970	0.85[EUR][1000 genomes]
rs2940912	0.92[EUR][1000 genomes]
rs2940914	0.85[EUR][1000 genomes]
rs2940916	1.00[CEU][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2940917	0.89[CEU][hapmap];0.83[EUR][1000 genomes]
rs2940918	0.89[CEU][hapmap];0.83[EUR][1000 genomes]
rs2940919	0.89[CEU][hapmap]
rs2940920	0.89[CEU][hapmap];0.83[YRI][hapmap];0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2940922	0.89[CEU][hapmap];0.83[EUR][1000 genomes]
rs2940926	0.89[CEU][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2940929	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2940931	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2940934	0.85[EUR][1000 genomes]
rs2940935	0.80[CEU][hapmap];0.82[EUR][1000 genomes]
rs2940939	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2940942	0.80[CEU][hapmap];0.82[EUR][1000 genomes]
rs2940943	0.80[CEU][hapmap];0.81[EUR][1000 genomes]
rs2972395	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2972400	1.00[CEU][hapmap];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2972404	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2972406	0.82[EUR][1000 genomes]
rs2972407	0.89[CEU][hapmap];0.85[EUR][1000 genomes]
rs2972410	0.83[EUR][1000 genomes]
rs2972411	0.89[CEU][hapmap];0.83[EUR][1000 genomes]
rs2972412	0.88[CEU][hapmap];0.83[EUR][1000 genomes]
rs2972413	0.89[CEU][hapmap];0.83[EUR][1000 genomes]
rs2972414	0.81[EUR][1000 genomes]
rs2972415	0.83[AFR][1000 genomes];0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2972416	0.89[CEU][hapmap];0.83[EUR][1000 genomes]
rs2972419	0.80[CEU][hapmap];0.82[EUR][1000 genomes]
rs34509769	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4642376	1.00[CEU][hapmap];0.89[GIH][hapmap];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4866890	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs60126365	0.81[EUR][1000 genomes]
rs61636452	0.82[EUR][1000 genomes]
rs62370648	0.81[EUR][1000 genomes]
rs6451614	0.93[EUR][1000 genomes]
rs6876736	0.81[EUR][1000 genomes]
rs6881436	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6884737	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7379192	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7704355	1.00[CEU][hapmap];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7728337	0.89[CEU][hapmap];0.83[EUR][1000 genomes]
rs9686286	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs974051	0.80[CEU][hapmap];0.84[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv933208	chr5:41879946-42876624	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	112 gene(s)	inside rSNPs	diseases
2	nsv492147	chr5:41902086-42896162	Enhancers Flanking Active TSS Active TSS Genic enhancers Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	113 gene(s)	inside rSNPs	diseases
3	nsv881375	chr5:42254097-42442715	Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv948514	chr5:42270161-42519262	Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:42425200-42428000	Weak transcription	Gastric	stomach
2	chr5:42425200-42430000	Weak transcription	Aorta	Aorta
3	chr5:42425400-42428200	Weak transcription	Spleen	Spleen
4	chr5:42425400-42429200	Weak transcription	Esophagus	oesophagus
5	chr5:42425600-42434200	Weak transcription	Left Ventricle	heart
6	chr5:42426000-42428000	Weak transcription	Fetal Intestine Small	intestine
7	chr5:42426000-42428000	Weak transcription	Right Atrium	heart
8	chr5:42426000-42430000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr5:42426400-42430000	Weak transcription	Right Ventricle	heart
10	chr5:42426600-42428000	Weak transcription	Psoas Muscle	Psoas
11	chr5:42426600-42428000	Weak transcription	Skeletal Muscle Female	skeletal muscle
12	chr5:42426600-42428600	Enhancers	Adipose Nuclei	Adipose
13	chr5:42426600-42429200	Weak transcription	Skeletal Muscle Male	skeletal muscle
14	chr5:42426600-42430000	Weak transcription	Ovary	ovary
15	chr5:42426600-42430000	Weak transcription	Rectal Smooth Muscle	rectum
16	chr5:42426600-42430200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr5:42426600-42430400	Weak transcription	Colon Smooth Muscle	Colon
18	chr5:42426600-42435200	Weak transcription	Fetal Muscle Leg	muscle
19	chr5:42426600-42436000	Weak transcription	Stomach Smooth Muscle	stomach
20	chr5:42427000-42430800	Enhancers	Liver	Liver
21	chr5:42427200-42429200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr5:42427400-42428000	Weak transcription	Fetal Stomach	stomach
23	chr5:42427400-42429800	Weak transcription	Fetal Lung	lung

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