Variant report

Variant	rs6710381
Chromosome Location	chr2:36898363-36898364
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:14)

rs_ID	r²[population]
rs1159961	0.91[AMR][1000 genomes]
rs12618264	0.91[AMR][1000 genomes]
rs1468808	0.90[AMR][1000 genomes]
rs2015020	0.91[AMR][1000 genomes]
rs2110877	0.91[AMR][1000 genomes]
rs2110878	0.91[AMR][1000 genomes]
rs2110880	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2160330	0.91[AMR][1000 genomes]
rs2192890	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4670156	0.91[AMR][1000 genomes]
rs4670583	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4670586	0.91[AMR][1000 genomes]
rs6745098	0.91[AMR][1000 genomes]
rs6752584	0.91[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1010985	chr2:36707157-36942066	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats 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	12 gene(s)	inside rSNPs	diseases
2	nsv535642	chr2:36707157-36942066	Genic enhancers Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS 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 miRNA target site	12 gene(s)	inside rSNPs	diseases
3	nsv1007757	chr2:36838387-37011384	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv535643	chr2:36838387-37011384	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv1004483	chr2:36875235-37356812	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
6	nsv535644	chr2:36875235-37356812	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
7	nsv963871	chr2:36896580-36913813	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 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	chr2:36892000-36900200	Weak transcription	A549	lung
2	chr2:36895800-36903600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr2:36897200-36898400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr2:36897600-36898800	Enhancers	Osteobl	bone
5	chr2:36897800-36898400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr2:36897800-36898600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr2:36897800-36898600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr2:36897800-36898600	Enhancers	HUVEC	blood vessel
9	chr2:36897800-36898800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr2:36897800-36898800	Enhancers	Placenta Amnion	Placenta Amnion
11	chr2:36897800-36899000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr2:36897800-36899200	Enhancers	Muscle Satellite Cultured Cells	--
13	chr2:36898000-36898400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr2:36898000-36898600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr2:36898000-36898600	Enhancers	NH-A	brain
16	chr2:36898000-36899200	Enhancers	HSMM	muscle
17	chr2:36898200-36898600	Enhancers	NHDF-Ad	bronchial
18	chr2:36898200-36898600	Enhancers	NHLF	lung

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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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