Variant report

Variant	rs17122442
Chromosome Location	chr1:62051934-62051935
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs12403275	0.90[AMR][1000 genomes]
rs12404794	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12407743	0.93[AMR][1000 genomes]
rs1495949	0.95[AMR][1000 genomes]
rs17122427	0.85[AMR][1000 genomes]
rs17122440	0.95[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17122451	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17122508	0.83[AMR][1000 genomes]
rs17122511	0.83[AMR][1000 genomes]
rs17122515	0.83[AMR][1000 genomes]
rs17122523	0.83[AMR][1000 genomes]
rs1933320	1.00[ASN][1000 genomes]
rs36121760	0.93[AMR][1000 genomes]
rs58893331	0.89[AMR][1000 genomes]
rs59748689	0.98[AMR][1000 genomes]
rs6688314	1.00[ASN][1000 genomes]
rs72921743	1.00[ASN][1000 genomes]
rs7545693	0.81[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs880254	0.93[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv994970	chr1:61693951-62199657	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
2	nsv1006142	chr1:61696142-62119763	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
3	nsv534980	chr1:61696142-62119763	Enhancers Flanking Active TSS Active TSS Strong transcription Weak transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
4	nsv916868	chr1:61700430-62119762	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
5	nsv1001052	chr1:61702011-62090670	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
6	nsv817402	chr1:61703965-62119762	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
7	nsv1010797	chr1:61703966-62125970	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
8	nsv530494	chr1:61723918-62084045	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
9	nsv1000294	chr1:61746280-62350718	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:62050600-62052200	Weak transcription	Esophagus	oesophagus
2	chr1:62050800-62052200	Enhancers	Hela-S3	cervix
3	chr1:62051000-62052200	Enhancers	HMEC	breast
4	chr1:62051000-62052400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr1:62051200-62052400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr1:62051600-62052400	Enhancers	NHEK	skin
7	chr1:62051600-62054000	Weak transcription	A549	lung
8	chr1:62051600-62054400	Weak transcription	Fetal Muscle Leg	muscle
9	chr1:62051600-62054800	Weak transcription	Stomach Mucosa	stomach
10	chr1:62051600-62057000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr1:62051800-62053600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr1:62051800-62053800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr1:62051800-62054200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr1:62051800-62054400	Weak transcription	Fetal Stomach	stomach
15	chr1:62051800-62054600	Weak transcription	Cortex derived primary cultured neurospheres	brain

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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