Variant report

Variant	rs73535810
Chromosome Location	chr6:110436868-110436869
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 67 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:62)

rs_ID	r²[population]
rs11153226	0.92[ASN][1000 genomes]
rs11751590	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11757055	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12110744	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12660119	0.85[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12660791	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12662013	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12665849	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12665858	0.94[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1462490	0.88[ASN][1000 genomes]
rs1462492	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1462493	0.84[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs2002630	0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4257894	0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs4299857	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4339500	0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4509164	0.91[ASN][1000 genomes]
rs4945850	0.84[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs4945851	0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs4947048	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4947051	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4947058	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs56122480	0.98[ASN][1000 genomes]
rs56135788	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs56287427	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs57983455	0.92[AFR][1000 genomes];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs60495849	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61020234	0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6568633	0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs6912291	0.82[ASN][1000 genomes]
rs6913554	0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6915379	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6918148	0.93[AFR][1000 genomes];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6925392	0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6926540	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6927667	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6927697	0.84[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs6927722	0.99[AFR][1000 genomes];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6928684	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6938106	0.89[ASN][1000 genomes]
rs6938139	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6938653	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs719849	0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73533834	0.88[ASN][1000 genomes]
rs73535817	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73535821	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73535837	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73535838	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73537927	0.92[ASN][1000 genomes]
rs73537938	0.92[ASN][1000 genomes]
rs73537949	0.93[AFR][1000 genomes];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7744828	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7747842	0.85[ASN][1000 genomes]
rs7766850	0.82[ASN][1000 genomes]
rs9372247	0.84[ASN][1000 genomes]
rs9372248	0.86[ASN][1000 genomes]
rs9374156	0.88[ASN][1000 genomes]
rs9400359	0.88[ASN][1000 genomes]
rs9400360	0.88[ASN][1000 genomes]
rs9481047	0.82[ASN][1000 genomes]
rs9487317	0.82[ASN][1000 genomes]
rs9487318	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv886535	chr6:110377006-110551463	Strong transcription Genic enhancers Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
2	esv2757188	chr6:110389926-110504680	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
3	esv2759462	chr6:110389926-110504680	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
4	esv1792799	chr6:110411065-110566597	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
5	nsv886536	chr6:110426046-110502831	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs73535810	WASF1	cis	Muscle Skeletal	GTEx
rs73535810	WASF1	cis	Artery Tibial	GTEx

Chromatin state (count:57 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:110417200-110438600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr6:110418800-110437200	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr6:110419000-110449600	Weak transcription	Brain Cingulate Gyrus	brain
4	chr6:110419000-110461800	Weak transcription	HSMMtube	muscle
5	chr6:110419200-110449600	Weak transcription	Brain Hippocampus Middle	brain
6	chr6:110423200-110440800	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr6:110423200-110448400	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr6:110423400-110437600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr6:110423400-110439000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr6:110423400-110445000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr6:110423400-110450000	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr6:110423400-110459000	Weak transcription	Fetal Stomach	stomach
13	chr6:110423400-110459200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr6:110423400-110459200	Weak transcription	Aorta	Aorta
15	chr6:110424600-110437800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr6:110424800-110443200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr6:110424800-110443200	Weak transcription	Ovary	ovary
18	chr6:110425000-110456400	Weak transcription	HUVEC	blood vessel
19	chr6:110425400-110440600	Weak transcription	Duodenum Smooth Muscle	Duodenum
20	chr6:110426000-110437200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr6:110426800-110448000	Weak transcription	Pancreas	Pancrea
22	chr6:110427600-110438400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr6:110427600-110459600	Weak transcription	NHEK	skin
24	chr6:110428200-110437200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr6:110428200-110437400	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chr6:110428200-110437600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
27	chr6:110428200-110443200	Weak transcription	Fetal Brain Female	brain
28	chr6:110428200-110450000	Weak transcription	HepG2	liver
29	chr6:110428400-110437400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr6:110428600-110437600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr6:110428800-110443000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr6:110428800-110446000	Weak transcription	Primary B cells from cord blood	blood
33	chr6:110429000-110445200	Weak transcription	Hela-S3	cervix
34	chr6:110429800-110453600	Weak transcription	Liver	Liver
35	chr6:110429800-110459200	Weak transcription	Stomach Smooth Muscle	stomach
36	chr6:110430000-110437600	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr6:110430000-110441400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr6:110430000-110443200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr6:110430000-110443200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr6:110430000-110443200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr6:110430000-110443600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
42	chr6:110430000-110446400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr6:110430000-110449800	Weak transcription	HUES48 Cell Line	embryonic stem cell
44	chr6:110430000-110452200	Weak transcription	Primary hematopoietic stem cells	blood
45	chr6:110430200-110446000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
46	chr6:110430400-110450200	Weak transcription	NHDF-Ad	bronchial
47	chr6:110431400-110459200	Weak transcription	HSMM	muscle
48	chr6:110433200-110443000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr6:110433200-110443200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr6:110433600-110437200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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