Variant report

Variant	rs72667830
Chromosome Location	chr1:56005610-56005611
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs17416725	0.84[EUR][1000 genomes]
rs17417072	0.84[EUR][1000 genomes]
rs41297891	0.84[EUR][1000 genomes]
rs41297893	0.84[EUR][1000 genomes]
rs55718597	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs55736946	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56058312	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs56161495	1.00[EUR][1000 genomes]
rs56237538	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs56246158	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57193275	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57832473	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61574505	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72667823	1.00[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs72667828	1.00[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs72667829	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72667831	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72667834	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72667835	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72667840	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72667842	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72667844	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72667851	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72667861	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72667865	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72667866	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72667868	0.92[EUR][1000 genomes]
rs72667875	0.92[EUR][1000 genomes]
rs72667878	0.84[EUR][1000 genomes]
rs72667893	0.92[EUR][1000 genomes]
rs72669719	0.84[EUR][1000 genomes]
rs72669723	0.84[EUR][1000 genomes]
rs72669726	0.84[EUR][1000 genomes]
rs72669728	0.84[EUR][1000 genomes]
rs72669729	0.84[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv10184	chr1:55728755-56084833	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:56002600-56007400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr1:56002600-56007600	Weak transcription	Osteobl	bone
3	chr1:56002600-56007800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr1:56002600-56007800	Weak transcription	NHLF	lung
5	chr1:56002600-56008000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr1:56002800-56007800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr1:56004800-56007600	Enhancers	Brain Angular Gyrus	brain
8	chr1:56005200-56006200	Enhancers	Left Ventricle	heart
9	chr1:56005200-56007000	Enhancers	Brain Hippocampus Middle	brain
10	chr1:56005400-56006200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr1:56005400-56006200	Enhancers	NHDF-Ad	bronchial
12	chr1:56005400-56007200	Enhancers	Brain Cingulate Gyrus	brain
13	chr1:56005400-56007200	Enhancers	Brain Inferior Temporal Lobe	brain
14	chr1:56005400-56007200	Enhancers	Brain Substantia Nigra	brain
15	chr1:56005600-56005800	Enhancers	Muscle Satellite Cultured Cells	--
16	chr1:56005600-56006200	Enhancers	Colon Smooth Muscle	Colon
17	chr1:56005600-56007800	Weak transcription	Psoas Muscle	Psoas
18	chr1:56005600-56010400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links