Variant report

Variant	rs10106298
Chromosome Location	chr8:103688381-103688382
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1076030	0.89[CEU][hapmap];0.82[EUR][1000 genomes]
rs13275089	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1434281	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1550005	0.92[CEU][hapmap];0.83[EUR][1000 genomes]
rs17773903	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2099408	0.89[CEU][hapmap];0.83[EUR][1000 genomes]
rs2436936	0.82[EUR][1000 genomes]
rs2436940	0.89[CEU][hapmap];0.82[EUR][1000 genomes]
rs3191333	0.92[CEU][hapmap];0.90[CHB][hapmap];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4281092	0.90[CHB][hapmap]
rs4734654	1.00[CEU][hapmap];0.90[CHB][hapmap];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7002992	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv33118	chr8:103358567-104068172	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	145 gene(s)	inside rSNPs	diseases
2	nsv1026755	chr8:103676970-103728556	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv1018625	chr8:103676970-103729197	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:103675400-103698200	Weak transcription	Osteobl	bone
2	chr8:103675600-103692800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr8:103679400-103689400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr8:103679800-103706400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr8:103687000-103688400	Weak transcription	Primary T helper cells PMA-I stimulated	--
6	chr8:103688000-103688800	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chr8:103688000-103688800	Enhancers	Lung	lung
8	chr8:103688200-103688800	Enhancers	Primary T helper cells fromperipheralblood	blood
9	chr8:103688200-103688800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
10	chr8:103688200-103688800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr8:103688200-103689000	Enhancers	Primary T helper memory cells from peripheral blood 1	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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