Variant report

Variant	rs2108153
Chromosome Location	chr7:13820978-13820979
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10950488	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11761278	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11762620	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11766318	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11768005	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11769506	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12670695	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs13224814	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs13237729	0.89[ASN][1000 genomes]
rs17167514	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs34012999	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs34492537	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs35297959	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs35454895	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs35505150	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs36041244	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs36198434	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs36200990	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs41318945	0.94[ASN][1000 genomes]
rs59756537	0.96[ASN][1000 genomes]
rs59760170	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62455263	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs62455264	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs62455265	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62455267	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6974368	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6974390	0.86[EUR][1000 genomes]
rs6974719	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7795241	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9770328	0.84[AMR][1000 genomes]
rs9771428	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830909	chr7:13692329-13868294	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv1019873	chr7:13707148-14133367	Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv1034411	chr7:13743365-13826756	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv433032	chr7:13792450-13911001	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv887696	chr7:13801825-13857235	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv525915	chr7:13819302-13841798	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv519601	chr7:13819968-13857235	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:13813200-13824200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr7:13818800-13824600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr7:13820000-13821800	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr7:13820800-13822000	Enhancers	HUES64 Cell Line	embryonic stem cell

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