Variant report

Variant	rs10748311
Chromosome Location	chr12:42113989-42113990
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10506207	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10785283	1.00[ASN][1000 genomes]
rs10880126	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1497181	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2167352	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs287008	0.81[EUR][1000 genomes]
rs287009	0.81[EUR][1000 genomes]
rs287025	0.82[EUR][1000 genomes]
rs3906840	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs3943523	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6582356	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv899040	chr12:41905897-42181706	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv832386	chr12:42017259-42189476	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv899043	chr12:42058138-42313665	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv899044	chr12:42058138-42321161	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:42103000-42118800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr12:42112600-42114400	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr12:42113200-42114000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr12:42113400-42114200	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr12:42113400-42114400	Enhancers	H1 Cell Line	embryonic stem cell
6	chr12:42113800-42114000	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr12:42113800-42114200	Weak transcription	Brain Germinal Matrix	brain
8	chr12:42113800-42114400	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr12:42113800-42114400	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr12:42113800-42114400	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr12:42113800-42114400	Enhancers	iPS-18 Cell Line	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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