Variant report

Variant	rs55814076
Chromosome Location	chr2:57674614-57674615
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:57669021..57671005-chr2:57673900..57675904,2	K562	blood:

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs1022365	0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13389938	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13390017	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13395074	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13403414	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13415195	0.85[EUR][1000 genomes]
rs1518678	0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs17039650	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17048828	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17048831	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17048835	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17195042	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17807763	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2090567	0.84[EUR][1000 genomes]
rs2310826	0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs57930441	0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs58806638	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59256639	0.84[EUR][1000 genomes]
rs60691185	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60940014	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66526851	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66647146	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6725986	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67509146	0.85[EUR][1000 genomes]
rs67754544	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67868906	0.85[EUR][1000 genomes]
rs67947086	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs68078812	0.85[EUR][1000 genomes]
rs68095793	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72814520	0.84[EUR][1000 genomes]
rs72814551	0.85[EUR][1000 genomes]
rs72814597	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72816503	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72937396	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72937402	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72939308	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7601574	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv999898	chr2:57193127-57901238	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv535729	chr2:57193127-57901238	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv1012285	chr2:57453353-57760750	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv874187	chr2:57507510-57703467	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv834126	chr2:57518655-57701015	Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv1000899	chr2:57537817-57694142	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv1007118	chr2:57562051-58147588	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
8	nsv1003020	chr2:57592640-57681816	Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv525779	chr2:57607449-57685889	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a
10	nsv1006603	chr2:57609335-57712494	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
11	nsv526359	chr2:57616965-57703467	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
12	nsv1001176	chr2:57618795-57770261	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:57671600-57676000	Weak transcription	Adipose Nuclei	Adipose
2	chr2:57671800-57676000	Weak transcription	HSMMtube	muscle
3	chr2:57672400-57675000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr2:57672400-57675200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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