Variant report

Variant	rs6985791
Chromosome Location	chr8:9983078-9983079
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 65 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs10104911	0.85[CHB][hapmap]
rs10107485	0.82[JPT][hapmap]
rs1160369	0.89[JPT][hapmap];0.90[ASN][1000 genomes]
rs11774411	1.00[CEU][hapmap];0.81[CHB][hapmap];0.94[JPT][hapmap];0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11783851	1.00[CEU][hapmap];0.81[CHB][hapmap];0.94[JPT][hapmap];0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11785434	0.82[ASN][1000 genomes]
rs11785454	0.88[ASN][1000 genomes]
rs11990610	0.90[CHB][hapmap]
rs11990614	0.90[CHB][hapmap]
rs12114195	0.83[ASN][1000 genomes]
rs12115063	0.83[ASN][1000 genomes]
rs12542030	0.83[ASN][1000 genomes]
rs12545469	0.86[CHB][hapmap];0.94[JPT][hapmap];0.89[ASN][1000 genomes]
rs12545775	1.00[CEU][hapmap];0.91[CHB][hapmap];0.84[JPT][hapmap];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12545788	1.00[CEU][hapmap];0.91[CHB][hapmap];0.84[JPT][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12547884	0.89[JPT][hapmap];0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12549943	1.00[CEU][hapmap];0.86[CHB][hapmap];0.89[JPT][hapmap];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12674871	1.00[CEU][hapmap];0.85[CHB][hapmap];0.89[JPT][hapmap];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12680389	0.81[CHB][hapmap]
rs13249013	0.84[JPT][hapmap]
rs13256357	1.00[CEU][hapmap];0.86[CHB][hapmap];0.89[JPT][hapmap];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1466555	0.82[JPT][hapmap];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1484645	0.91[CEU][hapmap];0.94[JPT][hapmap];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1564808	0.83[JPT][hapmap];0.84[ASN][1000 genomes]
rs17149332	0.86[CHB][hapmap]
rs17151108	0.85[CHB][hapmap];0.83[ASN][1000 genomes]
rs17151140	0.91[CHB][hapmap]
rs17151142	1.00[CEU][hapmap];0.91[CHB][hapmap];0.89[JPT][hapmap];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17151145	0.90[CHB][hapmap];0.85[ASN][1000 genomes]
rs17151147	0.90[CHB][hapmap];0.85[ASN][1000 genomes]
rs17151188	0.81[CHB][hapmap]
rs17151190	0.89[JPT][hapmap];0.82[ASN][1000 genomes]
rs17151201	0.91[CEU][hapmap];0.94[JPT][hapmap];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs17155393	1.00[CEU][hapmap];0.90[CHB][hapmap];0.84[JPT][hapmap];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1984863	0.86[CHB][hapmap];0.94[JPT][hapmap];0.89[ASN][1000 genomes]
rs1994223	0.85[CHB][hapmap]
rs1994224	0.85[CHB][hapmap]
rs2016221	0.87[ASN][1000 genomes]
rs2046398	0.85[CHB][hapmap]
rs2898242	0.89[JPT][hapmap];0.89[ASN][1000 genomes]
rs4840463	0.90[CHB][hapmap];0.89[JPT][hapmap];0.87[ASN][1000 genomes]
rs4841279	0.81[CHB][hapmap]
rs4841280	0.86[CHB][hapmap]
rs4841283	0.92[CEU][hapmap];0.90[CHB][hapmap];0.94[JPT][hapmap];0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6601417	0.86[CHB][hapmap];0.82[ASN][1000 genomes]
rs66602888	0.88[EUR][1000 genomes]
rs7008407	0.80[CHB][hapmap];0.94[JPT][hapmap];0.90[ASN][1000 genomes]
rs7008695	0.94[ASN][1000 genomes]
rs7012601	0.90[ASN][1000 genomes]
rs7016690	0.90[ASN][1000 genomes]
rs72626643	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7830843	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7843390	0.83[ASN][1000 genomes]
rs7843906	0.85[CHB][hapmap]
rs9329215	0.89[JPT][hapmap];0.90[ASN][1000 genomes]
rs936749	0.85[CHB][hapmap]
rs963593	0.85[CHB][hapmap];0.81[ASN][1000 genomes]
rs9644681	0.85[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][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	nsv916493	chr8:9806580-10029482	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv610263	chr8:9941021-10090149	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv1034343	chr8:9948342-10014155	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv831230	chr8:9953343-10139350	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	nsv1027280	chr8:9958259-10058984	Enhancers Active TSS Genic enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv1021921	chr8:9958259-10212555	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	esv1850829	chr8:9958321-10045451	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:9970600-9995800	Weak transcription	Pancreas	Pancrea
2	chr8:9975600-9987400	Weak transcription	Brain Germinal Matrix	brain
3	chr8:9977000-9988000	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr8:9978200-9988000	Weak transcription	Fetal Brain Female	brain
5	chr8:9980600-9988200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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