Variant report

Variant	rs17473314
Chromosome Location	chr6:15673730-15673731
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs1047631	1.00[CHB][hapmap]
rs13201824	1.00[JPT][hapmap]
rs2181435	1.00[CHB][hapmap]
rs2209863	1.00[JPT][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2619538	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs55913076	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs56360444	1.00[ASN][1000 genomes]
rs62395009	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62395012	0.87[ASN][1000 genomes]
rs62395013	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6914388	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs7742778	0.88[ASN][1000 genomes]
rs7755766	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7756911	0.88[ASN][1000 genomes]
rs9296989	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs9464815	0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv428136	chr6:15595640-15781241	Enhancers Genic enhancers Weak transcription Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	esv2755670	chr6:15624762-15736008	Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	esv2607475	chr6:15664805-15717086	Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	esv2757157	chr6:15668867-15725478	Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS	Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	esv2759408	chr6:15668867-15725478	Flanking Active TSS Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:15671800-15674800	Enhancers	Skeletal Muscle Female	skeletal muscle
2	chr6:15672400-15675200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr6:15672600-15674800	Enhancers	Skeletal Muscle Male	skeletal muscle
4	chr6:15672800-15674400	Weak transcription	Psoas Muscle	Psoas
5	chr6:15672800-15674600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr6:15672800-15674800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr6:15672800-15677200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr6:15673200-15674400	Weak transcription	Monocytes-CD14+_RO01746	blood
9	chr6:15673200-15674600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
10	chr6:15673200-15677400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr6:15673400-15673800	Weak transcription	Fetal Muscle Leg	muscle
12	chr6:15673600-15674000	Weak transcription	Primary monocytes fromperipheralblood	blood

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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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