Variant report

Variant	rs73861097
Chromosome Location	chr4:166502669-166502670
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10010500	0.93[ASN][1000 genomes]
rs12331357	0.82[ASN][1000 genomes]
rs17046878	0.93[ASN][1000 genomes]
rs28504688	0.93[ASN][1000 genomes]
rs73861094	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73861096	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73863214	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73863218	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73863219	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73863220	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73863221	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73863222	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73863223	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73863224	0.93[ASN][1000 genomes]
rs73863225	0.93[ASN][1000 genomes]
rs73863226	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73863227	1.00[AMR][1000 genomes]
rs73863228	0.93[ASN][1000 genomes]
rs73863230	0.93[ASN][1000 genomes]
rs73863232	1.00[AMR][1000 genomes]
rs73863237	0.93[ASN][1000 genomes]
rs73863241	1.00[AMR][1000 genomes]
rs73863242	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73863243	0.88[AFR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73863244	1.00[AMR][1000 genomes]
rs73863246	1.00[AMR][1000 genomes]
rs73863248	1.00[AMR][1000 genomes]
rs7438657	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9992328	0.93[ASN][1000 genomes]
rs9998651	0.93[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:166500600-166503000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr4:166500600-166504800	Enhancers	HMEC	breast
3	chr4:166500800-166503000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr4:166500800-166503000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr4:166501000-166503200	Enhancers	HUVEC	blood vessel
6	chr4:166501600-166502800	Weak transcription	Left Ventricle	heart
7	chr4:166501600-166502800	Weak transcription	Pancreas	Pancrea
8	chr4:166501600-166503600	Enhancers	NHEK	skin
9	chr4:166502000-166502800	Enhancers	HSMM	muscle
10	chr4:166502000-166502800	Enhancers	HSMMtube	muscle
11	chr4:166502000-166509000	Weak transcription	Colon Smooth Muscle	Colon
12	chr4:166502200-166502800	Enhancers	Fetal Heart	heart
13	chr4:166502200-166504600	Enhancers	Muscle Satellite Cultured Cells	--
14	chr4:166502400-166504000	Weak transcription	Osteobl	bone
15	chr4:166502400-166504600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr4:166502600-166503600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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