Variant report

Variant	rs6701782
Chromosome Location	chr1:213079941-213079942
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10779596	0.84[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10864024	0.96[ASN][1000 genomes]
rs10864030	0.86[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs11120063	0.93[ASN][1000 genomes]
rs12038555	0.98[ASN][1000 genomes]
rs12040492	0.98[ASN][1000 genomes]
rs12074192	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs12075289	0.93[ASN][1000 genomes]
rs12087098	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12135746	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12405742	0.88[ASN][1000 genomes]
rs12408694	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs12735579	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12760321	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1284851	0.93[ASN][1000 genomes]
rs1284853	0.93[ASN][1000 genomes]
rs1390501	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[ASN][1000 genomes]
rs15903	0.93[ASN][1000 genomes]
rs2359323	0.84[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2359326	0.83[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs2644549	0.98[ASN][1000 genomes]
rs2792562	0.98[ASN][1000 genomes]
rs4951473	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4951650	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4951651	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58128459	0.93[ASN][1000 genomes]
rs6660933	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6663568	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6663574	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6671740	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6674782	0.82[ASN][1000 genomes]
rs6677411	0.81[JPT][hapmap]
rs6679775	0.90[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs6682947	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs6683314	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[ASN][1000 genomes]
rs6697099	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6697126	0.93[ASN][1000 genomes]
rs7528113	0.81[JPT][hapmap]
rs7530057	0.89[ASN][1000 genomes]
rs7553536	0.90[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs9429894	0.93[ASN][1000 genomes]
rs9429895	0.93[ASN][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	nsv1008383	chr1:213025546-213114894	Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
2	nsv1007129	chr1:213037244-213083261	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:213073800-213089000	Weak transcription	Pancreas	Pancrea
2	chr1:213076800-213083600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr1:213078000-213080000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
4	chr1:213079000-213082600	Genic enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr1:213079200-213080000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr1:213079200-213081400	Genic enhancers	HUES64 Cell Line	embryonic stem cell
7	chr1:213079400-213080400	Enhancers	H1 Cell Line	embryonic stem cell
8	chr1:213079400-213080600	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr1:213079400-213081400	Genic enhancers	HUES48 Cell Line	embryonic stem cell
10	chr1:213079600-213080600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr1:213079600-213080600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr1:213079600-213081200	Genic enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr1:213079600-213090000	Weak transcription	Right Atrium	heart
14	chr1:213079800-213080600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr1:213079800-213082400	Genic enhancers	HUES6 Cell Line	embryonic stem cell
16	chr1:213079800-213082400	Enhancers	iPS-15b Cell Line	embryonic stem cell

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