Variant report

Variant	rs2355106
Chromosome Location	chr7:11874058-11874059
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10224053	0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10228370	0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10232241	0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10241322	0.93[ASN][1000 genomes]
rs11979135	0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2355107	0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2355111	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2883596	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35302727	0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4721016	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6942789	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6966075	0.93[ASN][1000 genomes]
rs6978088	1.00[CEU][hapmap];0.84[CHB][hapmap];1.00[JPT][hapmap];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7458129	0.95[EUR][1000 genomes];0.85[ASN][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	nsv606199	chr7:11506143-12486659	Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv887614	chr7:11778424-12211198	Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
3	nsv830905	chr7:11793513-11941594	Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
4	nsv606203	chr7:11870711-11915630	Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv887615	chr7:11870711-11938060	Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:11872200-11875200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr7:11872400-11874200	Enhancers	Primary hematopoietic stem cells	blood
3	chr7:11873600-11874800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr7:11873600-11876800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr7:11873800-11874200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr7:11873800-11874400	Enhancers	A549	lung
7	chr7:11873800-11875200	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr7:11873800-11875200	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr7:11873800-11875200	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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