Variant report

Variant	rs3010415
Chromosome Location	chr9:108609872-108609873
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:108609147..108611784-chr9:109960559..109962300,2	K562	blood:

Extended variants
information (count: 90 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:82)

rs_ID	r²[population]
rs10114077	0.82[CHB][hapmap]
rs10117187	0.82[CHB][hapmap]
rs10118661	0.82[CHB][hapmap]
rs10122308	0.85[CHB][hapmap]
rs10156569	0.82[CHB][hapmap]
rs10156571	0.82[CHB][hapmap]
rs10512340	0.82[CHB][hapmap]
rs10739213	0.81[CHB][hapmap]
rs10739214	0.94[ASN][1000 genomes]
rs10759128	0.82[CHB][hapmap]
rs10759132	0.82[CHB][hapmap]
rs10759133	0.81[CHB][hapmap]
rs10759135	0.82[CHB][hapmap]
rs10759145	0.81[ASN][1000 genomes]
rs10759146	0.82[ASN][1000 genomes]
rs10759147	0.94[ASN][1000 genomes]
rs10816299	0.82[CHB][hapmap]
rs10816300	0.82[CHB][hapmap]
rs10816302	0.82[CHB][hapmap]
rs10816310	0.82[CHB][hapmap]
rs10816313	0.87[CHB][hapmap]
rs10816319	0.82[CHB][hapmap]
rs10816324	0.82[CHB][hapmap]
rs10816349	0.94[ASN][1000 genomes]
rs10816350	0.92[ASN][1000 genomes]
rs10978220	0.82[CHB][hapmap]
rs10978226	0.82[CHB][hapmap]
rs10978230	0.82[CHB][hapmap]
rs10978235	0.82[CHB][hapmap]
rs10978239	0.82[CHB][hapmap]
rs10978240	0.82[CHB][hapmap]
rs10978241	0.85[CHB][hapmap]
rs10978309	0.94[ASN][1000 genomes]
rs10978310	0.94[ASN][1000 genomes]
rs10978311	0.94[ASN][1000 genomes]
rs10978312	0.94[ASN][1000 genomes]
rs10978313	0.92[ASN][1000 genomes]
rs12338851	0.82[CHB][hapmap]
rs12345343	0.82[CHB][hapmap]
rs12347783	0.82[CHB][hapmap]
rs12684672	0.84[CHB][hapmap]
rs13286237	0.82[CHB][hapmap]
rs1806663	0.92[ASN][1000 genomes]
rs1806664	0.92[ASN][1000 genomes]
rs1979992	0.82[CHB][hapmap]
rs1979993	0.82[CHB][hapmap]
rs2175121	0.82[CHB][hapmap]
rs2175122	0.82[CHB][hapmap]
rs2271246	0.82[CHB][hapmap]
rs2417646	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2417647	0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28534814	1.00[ASN][1000 genomes]
rs2997726	0.90[ASN][1000 genomes]
rs2997727	0.89[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs3010964	0.80[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs3105991	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3817141	0.82[CHB][hapmap]
rs6477455	0.82[CHB][hapmap]
rs6477462	0.82[CHB][hapmap]
rs6477463	0.82[CHB][hapmap]
rs7019053	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7020523	0.82[CHB][hapmap]
rs7024988	0.86[CEU][hapmap];0.96[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7026814	0.82[CHB][hapmap]
rs7026968	0.82[CHB][hapmap]
rs7030636	0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7031360	0.81[CHB][hapmap]
rs7031431	0.82[CHB][hapmap]
rs7046212	0.82[CHB][hapmap]
rs7046293	0.82[CHB][hapmap]
rs71501939	0.99[ASN][1000 genomes]
rs7854091	0.94[ASN][1000 genomes]
rs7854144	0.94[ASN][1000 genomes]
rs7862281	0.98[ASN][1000 genomes]
rs7865672	0.95[CHB][hapmap];0.91[JPT][hapmap];0.98[ASN][1000 genomes]
rs7869341	0.94[ASN][1000 genomes]
rs7869461	0.94[ASN][1000 genomes]
rs7873663	0.82[CHB][hapmap]
rs7875434	0.82[CHB][hapmap]
rs9299115	0.91[ASN][1000 genomes]
rs9777628	0.82[CHB][hapmap]
rs9969715	0.82[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv893693	chr9:108427062-108683134	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv893694	chr9:108486533-108854018	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv1041073	chr9:108535813-108731343	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
4	nsv508558	chr9:108536115-108611087	ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region miRNA target site	1 gene(s)	inside rSNPs	n/a
5	nsv1036849	chr9:108582944-108651205	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv1052684	chr9:108582944-108730280	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv615140	chr9:108592589-108725567	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv831679	chr9:108603112-108785347	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:108598400-108615600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr9:108609600-108616000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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