Variant report

Variant	rs35361206
Chromosome Location	chr8:91515481-91515482
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs1028255	0.81[EUR][1000 genomes]
rs10504894	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12545726	0.84[EUR][1000 genomes]
rs12674903	0.83[EUR][1000 genomes]
rs12678527	0.91[EUR][1000 genomes]
rs13268721	0.84[EUR][1000 genomes]
rs1476427	0.84[EUR][1000 genomes]
rs2105965	0.85[EUR][1000 genomes]
rs2187982	0.84[EUR][1000 genomes]
rs2205151	0.84[EUR][1000 genomes]
rs2205152	0.84[EUR][1000 genomes]
rs2213886	0.84[EUR][1000 genomes]
rs2285231	0.85[EUR][1000 genomes]
rs2879361	0.81[EUR][1000 genomes]
rs35816262	0.86[EUR][1000 genomes]
rs3950221	0.84[EUR][1000 genomes]
rs4735190	0.86[EUR][1000 genomes]
rs4735201	0.90[EUR][1000 genomes]
rs56784954	0.85[EUR][1000 genomes]
rs6471113	0.80[EUR][1000 genomes]
rs6986088	0.85[EUR][1000 genomes]
rs6988302	0.81[EUR][1000 genomes]
rs6988733	0.85[EUR][1000 genomes]
rs6989123	0.84[EUR][1000 genomes]
rs6993715	0.90[EUR][1000 genomes]
rs6995399	0.81[EUR][1000 genomes]
rs7000724	0.87[EUR][1000 genomes]
rs7017295	0.81[EUR][1000 genomes]
rs7017630	0.81[EUR][1000 genomes]
rs7812970	0.85[EUR][1000 genomes]
rs7817954	0.85[EUR][1000 genomes]
rs7824376	0.91[EUR][1000 genomes]
rs7824511	0.91[EUR][1000 genomes]
rs9643298	0.84[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2408826	chr8:91515233-91515898	Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
2	esv3479615	chr8:91515295-91515789	Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
3	esv3497933	chr8:91515312-91515782	Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
4	esv3497935	chr8:91515326-91515791	Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
5	esv3497934	chr8:91515345-91515720	Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
6	esv3479613	chr8:91515351-91515756	Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
7	esv3479612	chr8:91515365-91515711	Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
8	esv3370856	chr8:91515388-91515721	Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
9	esv3479614	chr8:91515400-91515689	Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
10	esv3479616	chr8:91515415-91515701	Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
11	esv3497936	chr8:91515422-91515692	Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:91510000-91516600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:91514200-91516400	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr8:91515400-91516600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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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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