Variant report

Variant	rs34226838
Chromosome Location	chr1:210712448-210712449
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs12122837	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12124286	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12130516	0.94[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs12131405	0.91[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs12139453	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12142819	0.83[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs12754753	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17188344	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17188367	0.85[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2357920	0.91[AMR][1000 genomes]
rs34542042	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs4132902	0.88[ASN][1000 genomes]
rs4344331	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][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	nsv873148	chr1:210665583-210994339	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
2	nsv549106	chr1:210698719-210736508	Enhancers Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv1011702	chr1:210706323-210739030	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	esv988198	chr1:210707300-210716552	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:210674400-210719600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr1:210680600-210731000	Weak transcription	HSMM	muscle
3	chr1:210709400-210715200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr1:210709800-210715200	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr1:210710000-210715000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr1:210710000-210715000	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr1:210710000-210715000	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr1:210710000-210715200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr1:210710000-210715200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr1:210710000-210715400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr1:210710200-210715200	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr1:210710200-210715200	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr1:210710200-210715200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr1:210710400-210715200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr1:210710600-210715200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr1:210710800-210719000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr1:210711000-210715000	Weak transcription	HSMMtube	muscle

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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