Variant report

Variant	rs34262449
Chromosome Location	chr2:67484635-67484636
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs13008890	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs13015287	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1384743	0.83[AFR][1000 genomes]
rs1384744	0.83[AFR][1000 genomes]
rs17601386	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs17603029	0.83[AFR][1000 genomes]
rs34286589	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs62146349	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62156538	0.83[AFR][1000 genomes]
rs62156540	0.83[AFR][1000 genomes]
rs62156541	0.83[AFR][1000 genomes]
rs62158282	0.83[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1008584	chr2:67168244-67703601	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
2	nsv535775	chr2:67168244-67703601	Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
3	nsv534389	chr2:67388428-68225338	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
4	nsv1001672	chr2:67429146-67498042	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:67474400-67486200	Weak transcription	Rectal Smooth Muscle	rectum
2	chr2:67482400-67488200	Enhancers	Hela-S3	cervix
3	chr2:67482800-67486200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr2:67483600-67486200	Weak transcription	HUVEC	blood vessel
5	chr2:67483600-67486800	Weak transcription	HSMMtube	muscle
6	chr2:67484000-67486200	Weak transcription	NHLF	lung
7	chr2:67484000-67486600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr2:67484000-67486800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr2:67484200-67485800	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr2:67484200-67486000	Weak transcription	NH-A	brain
11	chr2:67484200-67486200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr2:67484200-67486200	Weak transcription	HMEC	breast
13	chr2:67484200-67486200	Weak transcription	NHEK	skin
14	chr2:67484200-67486200	Weak transcription	Osteobl	bone
15	chr2:67484200-67487000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr2:67484400-67485400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr2:67484600-67487600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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