Variant report

Variant	rs6581320
Chromosome Location	chr12:60870034-60870035
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10877438	0.85[EUR][1000 genomes]
rs11173485	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11173492	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12310057	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2723742	0.81[AFR][1000 genomes]
rs4297503	0.89[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4372489	0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4622306	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4758865	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7131721	0.89[AFR][1000 genomes];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7131951	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7300335	0.89[AFR][1000 genomes];0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7312791	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[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	nsv1047466	chr12:60702221-61521156	Active TSS Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv832432	chr12:60801619-60968907	Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv899138	chr12:60848962-60966997	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv826399	chr12:60858170-60900139	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv559137	chr12:60858680-60947395	Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:60868600-60870600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
2	chr12:60869000-60870600	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr12:60869000-60870600	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr12:60869200-60870200	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr12:60869200-60870200	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr12:60869400-60870600	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr12:60869600-60870600	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr12:60869800-60870200	Flanking Active TSS	HUES48 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