Variant report

Variant	rs932919
Chromosome Location	chr1:104634610-104634611
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 70 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10494005	0.87[ASN][1000 genomes]
rs10494006	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11185378	0.87[ASN][1000 genomes]
rs11185379	0.87[ASN][1000 genomes]
rs11588998	0.87[ASN][1000 genomes]
rs11591213	0.86[ASN][1000 genomes]
rs11810951	0.87[ASN][1000 genomes]
rs12026039	0.83[ASN][1000 genomes]
rs12031339	0.83[ASN][1000 genomes]
rs12031508	0.83[ASN][1000 genomes]
rs12046317	0.85[ASN][1000 genomes]
rs12046379	0.87[ASN][1000 genomes]
rs12049463	0.85[ASN][1000 genomes]
rs12730463	0.88[ASN][1000 genomes]
rs12746031	0.88[ASN][1000 genomes]
rs1330395	0.87[ASN][1000 genomes]
rs1330396	0.87[ASN][1000 genomes]
rs1330397	0.87[ASN][1000 genomes]
rs1330398	0.88[ASN][1000 genomes]
rs1411469	0.88[ASN][1000 genomes]
rs1576518	0.88[ASN][1000 genomes]
rs17018271	0.87[ASN][1000 genomes]
rs17018274	0.87[ASN][1000 genomes]
rs1999225	0.87[ASN][1000 genomes]
rs1999227	0.87[ASN][1000 genomes]
rs1999228	0.87[ASN][1000 genomes]
rs2065190	0.88[ASN][1000 genomes]
rs2076824	0.87[ASN][1000 genomes]
rs2316920	0.87[ASN][1000 genomes]
rs2316922	0.87[ASN][1000 genomes]
rs28457806	0.87[ASN][1000 genomes]
rs3811505	0.81[ASN][1000 genomes]
rs3811506	0.81[ASN][1000 genomes]
rs3968403	0.83[ASN][1000 genomes]
rs5005718	0.87[ASN][1000 genomes]
rs5005719	0.87[ASN][1000 genomes]
rs5005720	0.87[ASN][1000 genomes]
rs5005723	0.84[ASN][1000 genomes]
rs5005724	0.84[ASN][1000 genomes]
rs5005725	0.87[ASN][1000 genomes]
rs61788840	0.88[ASN][1000 genomes]
rs6672662	0.87[ASN][1000 genomes]
rs6682812	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs67847517	0.87[ASN][1000 genomes]
rs729106	0.87[ASN][1000 genomes]
rs729107	0.87[ASN][1000 genomes]
rs932920	0.88[ASN][1000 genomes]
rs932921	0.87[ASN][1000 genomes]
rs944229	0.87[ASN][1000 genomes]
rs978288	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs978289	0.86[ASN][1000 genomes]
rs9804093	0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1824711	chr1:103990359-104650457	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv534091	chr1:104092317-104642037	Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
3	nsv1014507	chr1:104307231-104784753	Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1012931	chr1:104322484-104778961	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv872072	chr1:104470622-105076810	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv1010903	chr1:104483363-105468941	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv872073	chr1:104502333-104719055	Enhancers ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv1002973	chr1:104546037-104641567	Enhancers Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
9	nsv1002477	chr1:104546037-104657872	Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
10	nsv1005132	chr1:104546037-104675264	Weak transcription Enhancers Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
11	nsv1014933	chr1:104549412-104657872	Enhancers Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
12	nsv999512	chr1:104550664-104644557	Enhancers Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
13	nsv1006914	chr1:104563498-104657872	Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
14	nsv1000500	chr1:104571819-104657872	Enhancers Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
15	nsv1008275	chr1:104573592-104644557	Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
16	esv1834182	chr1:104576359-104672830	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
17	esv1839044	chr1:104576359-104707906	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
18	nsv482341	chr1:104589525-104731812	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:104634400-104635800	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr1:104634600-104635000	Enhancers	H9 Cell Line	embryonic stem cell
3	chr1:104634600-104635600	Enhancers	H1 Cell Line	embryonic stem cell
4	chr1:104634600-104635800	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr1:104634600-104635800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr1:104634600-104636000	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr1:104634600-104636000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr1:104634600-104636200	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr1:104634600-104636400	Enhancers	iPS-20b Cell Line	embryonic stem cell

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