Variant report

Variant	rs910355
Chromosome Location	chr6:73450321-73450322
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs16882791	0.82[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16882804	1.00[EUR][1000 genomes]
rs16882811	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16882816	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2185766	1.00[MEX][hapmap]
rs73753900	1.00[EUR][1000 genomes]
rs7749632	1.00[EUR][1000 genomes]
rs7765507	1.00[EUR][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	nsv1023809	chr6:73157813-73477997	Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv538303	chr6:73157813-73477997	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv830689	chr6:73385557-73544404	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv830690	chr6:73391428-73574304	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv886154	chr6:73442239-73471683	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:73437800-73455200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr6:73438400-73455400	Weak transcription	HMEC	breast
3	chr6:73443200-73455400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr6:73448400-73451800	Enhancers	Primary B cells from peripheral blood	blood
5	chr6:73448800-73450800	Enhancers	Monocytes-CD14+_RO01746	blood
6	chr6:73449000-73450400	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr6:73449600-73451200	Enhancers	Primary B cells from cord blood	blood
8	chr6:73449600-73451200	Flanking Active TSS	GM12878-XiMat	blood
9	chr6:73449600-73451600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr6:73449600-73452600	Enhancers	Psoas Muscle	Psoas
11	chr6:73449800-73450800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr6:73450000-73458400	Weak transcription	Primary hematopoietic stem cells	blood
13	chr6:73450200-73451200	Enhancers	Primary T cells fromperipheralblood	blood
14	chr6:73450200-73451200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
15	chr6:73450200-73451600	Enhancers	Skeletal Muscle Female	skeletal muscle
16	chr6:73450200-73455000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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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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