Variant report

Variant	rs1359956
Chromosome Location	chr9:16044097-16044098
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 94 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:88)

rs_ID	r²[population]
rs1014307	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10733306	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10733307	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10738419	0.80[TSI][hapmap]
rs10738423	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10738424	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10738425	0.81[AFR][1000 genomes];0.99[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10738426	0.92[CEU][hapmap];0.94[CHB][hapmap];0.89[JPT][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10738427	0.92[CEU][hapmap];0.94[CHB][hapmap];0.89[JPT][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.99[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10738428	0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10738430	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10756720	0.83[TSI][hapmap]
rs10756726	0.80[TSI][hapmap]
rs10756728	0.80[TSI][hapmap]
rs10756729	0.82[TSI][hapmap]
rs10756734	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10756735	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10756736	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10756737	0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10756738	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10756739	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10756741	0.92[CEU][hapmap];0.94[CHB][hapmap];0.89[JPT][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.99[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10756742	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10810461	0.82[TSI][hapmap]
rs10810484	0.83[TSI][hapmap]
rs10810488	0.83[TSI][hapmap]
rs10810502	0.80[TSI][hapmap]
rs10810509	0.80[TSI][hapmap]
rs10810517	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10810518	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10810519	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10810520	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10810521	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10810522	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10810523	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10810524	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10810526	0.92[CEU][hapmap];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10810527	0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10810528	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10962260	0.92[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11788695	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12379466	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1328273	0.82[EUR][1000 genomes]
rs1328274	0.82[EUR][1000 genomes]
rs1328275	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1328276	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1328277	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1328278	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1328279	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1328280	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1328296	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1328298	0.83[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1359954	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1359957	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1410450	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1410451	0.92[CEU][hapmap];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1410452	0.92[CEU][hapmap];0.94[CHB][hapmap];0.89[JPT][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.99[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1410453	0.92[CEU][hapmap];0.94[CHB][hapmap];0.89[JPT][hapmap]
rs1410454	0.92[ASW][hapmap];0.92[CEU][hapmap];0.94[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.89[JPT][hapmap];0.95[MEX][hapmap];0.98[TSI][hapmap];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1410455	0.92[CEU][hapmap];0.94[CHB][hapmap];0.89[JPT][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.99[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1887666	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1887667	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1887668	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1887669	0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1891212	0.85[TSI][hapmap]
rs1984246	0.85[TSI][hapmap]
rs2026661	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2149233	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2382551	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4247294	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4740631	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4740632	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4741557	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4741558	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4741559	0.92[CEU][hapmap];0.94[CHB][hapmap];0.89[JPT][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.99[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4741560	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4741561	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7027202	0.85[TSI][hapmap]
rs7040690	0.92[CEU][hapmap];0.87[CHB][hapmap];0.83[JPT][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.99[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs752489	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs752490	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs769151	0.80[TSI][hapmap]
rs7873925	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs943787	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs943788	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs943789	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9792412	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs997410	0.94[CHB][hapmap];0.89[JPT][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[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	nsv892625	chr9:15326251-16064850	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv892637	chr9:15926508-16060746	Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv949463	chr9:15970668-16377360	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv831521	chr9:15974174-16106565	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv1025555	chr9:16022186-16064158	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	esv2761506	chr9:16040491-16093736	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs1359956	C9orf93	cis	cerebellum	SCAN

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:16030800-16050000	Weak transcription	Aorta	Aorta
2	chr9:16040600-16057600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr9:16041200-16044800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr9:16041200-16049600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr9:16041400-16044600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr9:16041400-16045400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr9:16041400-16046200	Weak transcription	Fetal Intestine Large	intestine
8	chr9:16041400-16048000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr9:16042600-16044600	Weak transcription	Fetal Muscle Trunk	muscle
10	chr9:16043200-16046000	Enhancers	Fetal Stomach	stomach
11	chr9:16043400-16045600	Enhancers	Osteobl	bone
12	chr9:16043400-16045800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr9:16043400-16046000	Enhancers	Fetal Kidney	kidney
14	chr9:16043400-16046400	Enhancers	Muscle Satellite Cultured Cells	--
15	chr9:16043600-16044200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr9:16043600-16045000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr9:16043600-16045400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr9:16043600-16045600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr9:16043600-16045800	Enhancers	Adipose Nuclei	Adipose
20	chr9:16043600-16045800	Enhancers	Hela-S3	cervix
21	chr9:16043800-16044200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr9:16043800-16044200	Enhancers	Right Atrium	heart
23	chr9:16043800-16044200	Enhancers	NHLF	lung
24	chr9:16043800-16044800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr9:16043800-16044800	Enhancers	Fetal Lung	lung
26	chr9:16043800-16045600	Enhancers	Fetal Muscle Leg	muscle
27	chr9:16043800-16045600	Enhancers	HSMM	muscle
28	chr9:16044000-16044800	Enhancers	HUVEC	blood vessel
29	chr9:16044000-16045000	Enhancers	NH-A	brain
30	chr9:16044000-16045400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
31	chr9:16044000-16045600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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