Variant report

Variant	rs34274138
Chromosome Location	chr2:208972790-208972791
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10178641	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10188278	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10188286	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10198963	0.81[EUR][1000 genomes]
rs1020581	0.95[ASN][1000 genomes]
rs10497893	0.99[ASN][1000 genomes]
rs11677829	0.92[ASN][1000 genomes]
rs11684908	0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11690797	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13006347	0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13008550	0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13034094	0.95[ASN][1000 genomes]
rs1806338	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2084872	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34126491	0.90[ASN][1000 genomes]
rs34577840	0.95[ASN][1000 genomes]
rs34589201	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34765959	0.95[ASN][1000 genomes]
rs35934862	0.81[ASN][1000 genomes]
rs35960349	0.96[ASN][1000 genomes]
rs55770589	0.95[ASN][1000 genomes]
rs55999272	0.89[ASN][1000 genomes]
rs60163320	0.95[ASN][1000 genomes]
rs6435407	0.88[ASN][1000 genomes]
rs6435411	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6709879	0.95[ASN][1000 genomes]
rs6716279	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6744189	0.88[ASN][1000 genomes]
rs6745137	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6745370	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6747966	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6751131	0.93[ASN][1000 genomes]
rs6757791	0.87[ASN][1000 genomes]
rs6758319	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6759995	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6761316	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs67900982	0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs732008	0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs732009	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7349197	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7586866	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7586953	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7587397	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7589556	0.82[EUR][1000 genomes]
rs7590593	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7604207	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1010531	chr2:208610639-209176782	Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Genic enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
2	nsv536130	chr2:208610639-209176782	Weak transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Active TSS Genic enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
3	nsv534496	chr2:208814372-209302791	Strong transcription Active TSS Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
4	nsv875744	chr2:208952810-208994045	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv875745	chr2:208969865-208994045	Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv875746	chr2:208971007-208989708	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:208965000-208976600	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr2:208967400-208976800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr2:208969400-208976600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr2:208972000-208973000	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr2:208972000-208973000	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr2:208972000-208973200	Enhancers	H1 Cell Line	embryonic stem cell
7	chr2:208972000-208973200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr2:208972200-208972800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr2:208972600-208976200	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr2:208972600-208976600	Weak transcription	HUES48 Cell Line	embryonic stem cell

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