Variant report

Variant	rs1212995
Chromosome Location	chr13:95421669-95421670
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 1 )

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

rs_ID	r²[population]
rs1189268	0.98[ASN][1000 genomes]
rs1203222	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12868463	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1408647	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17196401	0.98[ASN][1000 genomes]
rs2209074	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs701606	0.87[JPT][hapmap]
rs701607	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7328165	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7329702	0.88[ASN][1000 genomes]
rs792297	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs792298	0.87[JPT][hapmap]
rs792299	1.00[CEU][hapmap];0.89[YRI][hapmap];0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9590073	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832687	chr13:95412811-95582161	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	esv2763049	chr13:95414554-95445266	Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs1212995	DCT	cis	cerebellum	SCAN

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:95418600-95422200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr13:95420800-95421800	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr13:95421000-95422200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr13:95421000-95422800	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr13:95421200-95422200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr13:95421200-95422400	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr13:95421600-95421800	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr13:95421600-95421800	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr13:95421600-95422000	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr13:95421600-95423000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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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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