Variant report

Variant	rs28565131
Chromosome Location	chr1:169610606-169610607
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs3917658	1.00[AMR][1000 genomes]
rs3917772	1.00[AMR][1000 genomes]
rs3917812	1.00[AMR][1000 genomes]
rs3917814	1.00[AMR][1000 genomes]
rs59251103	1.00[AMR][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	esv10418	chr1:169059628-169621268	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription 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	56 gene(s)	inside rSNPs	diseases
2	nsv532586	chr1:169593222-169713184	Weak transcription Transcr. at gene 5' and 3' Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv159209	chr1:169607718-169613389	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:169605200-169617000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr1:169609000-169616400	Weak transcription	Primary T helper cells PMA-I stimulated	--
3	chr1:169609000-169616800	Weak transcription	Primary T helper cells fromperipheralblood	blood
4	chr1:169609800-169611800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr1:169610000-169611600	Enhancers	Primary hematopoietic stem cells	blood
6	chr1:169610000-169612000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr1:169610600-169610800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr1:169610600-169611600	Enhancers	Dnd41	blood
9	chr1:169610600-169611800	Enhancers	Primary B cells from peripheral blood	blood

Quick Search:

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

what's new

Quick links