Variant report

Variant	rs74133655
Chromosome Location	chr1:196254200-196254201
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs11802442	0.94[AFR][1000 genomes]
rs11802997	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11803170	1.00[AFR][1000 genomes]
rs11805373	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11806027	1.00[AFR][1000 genomes]
rs11806585	1.00[AFR][1000 genomes]
rs11809793	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35084486	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55797122	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56287411	0.84[AFR][1000 genomes]
rs57962893	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58760665	0.84[AFR][1000 genomes]
rs60185937	1.00[AFR][1000 genomes]
rs74133630	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74133633	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74133635	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74133636	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74133641	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74133642	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74133644	0.97[AFR][1000 genomes]
rs74133650	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74136503	1.00[AFR][1000 genomes]
rs74136506	1.00[AFR][1000 genomes]
rs74136508	0.91[AFR][1000 genomes]
rs74136511	1.00[AFR][1000 genomes]
rs74136514	1.00[AFR][1000 genomes]
rs74136530	0.97[AFR][1000 genomes]
rs74136531	0.87[AFR][1000 genomes]
rs74136532	0.84[AFR][1000 genomes]
rs74136534	0.84[AFR][1000 genomes]
rs74136536	0.84[AFR][1000 genomes]
rs74136537	0.84[AFR][1000 genomes]
rs74136538	0.84[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv872952	chr1:196174790-196304223	Strong transcription Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv548741	chr1:196186750-196293493	Bivalent Enhancer Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv832237	chr1:196205674-196328500	Enhancers Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:196234800-196255400	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr1:196244600-196272400	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr1:196249200-196281400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr1:196250600-196258400	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr1:196250800-196255400	Weak transcription	Ovary	ovary
6	chr1:196250800-196271600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr1:196251000-196271600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr1:196251800-196255600	Weak transcription	Liver	Liver
9	chr1:196251800-196261400	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr1:196252200-196272200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr1:196253200-196271600	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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