Variant report

Variant	rs7035931
Chromosome Location	chr9:93966276-93966277
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10512206	0.93[ASN][1000 genomes]
rs10991813	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10991816	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10991820	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10991826	0.91[ASN][1000 genomes]
rs10991835	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12236714	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12236715	0.93[ASN][1000 genomes]
rs12238485	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3884186	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3914139	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs59546704	0.93[ASN][1000 genomes]
rs7020997	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7025775	0.92[ASN][1000 genomes]
rs7026063	0.91[ASN][1000 genomes]
rs7036028	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9792456	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:93959800-93969600	Weak transcription	Gastric	stomach
2	chr9:93961000-93969400	Weak transcription	Osteobl	bone
3	chr9:93961000-93969800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr9:93961200-93969200	Weak transcription	Liver	Liver
5	chr9:93961200-93969600	Weak transcription	Right Atrium	heart
6	chr9:93961200-93975600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr9:93962400-93969800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr9:93962400-93969800	Weak transcription	K562	blood
9	chr9:93962600-93969600	Weak transcription	Stomach Mucosa	stomach
10	chr9:93963200-93969800	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr9:93965200-93968800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr9:93965400-93968800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr9:93965400-93969600	Weak transcription	Fetal Lung	lung
14	chr9:93965400-93969600	Weak transcription	Psoas Muscle	Psoas
15	chr9:93965800-93969400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr9:93966200-93967000	Enhancers	HepG2	liver

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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