Variant report

Variant	rs474800
Chromosome Location	chr5:89861312-89861313
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:89854805..89859362-chr5:89860971..89864483,4	K562	blood:

Extended variants
information (count: 71 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:60)

rs_ID	r²[population]
rs10058765	0.84[ASN][1000 genomes]
rs10060427	0.84[ASN][1000 genomes]
rs10062714	0.84[ASN][1000 genomes]
rs10062924	0.84[ASN][1000 genomes]
rs10072105	0.84[ASN][1000 genomes]
rs10473936	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1047787	0.82[EUR][1000 genomes]
rs10514328	0.88[ASN][1000 genomes]
rs10942597	0.81[EUR][1000 genomes]
rs11741740	0.94[ASN][1000 genomes]
rs12516985	0.84[ASN][1000 genomes]
rs13182165	0.85[EUR][1000 genomes]
rs13185955	0.84[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1673378	0.84[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1673379	0.86[ASN][1000 genomes]
rs16868957	0.84[ASN][1000 genomes]
rs1700510	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1700511	0.88[ASN][1000 genomes]
rs1812737	0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2366773	0.84[ASN][1000 genomes]
rs2366774	0.84[ASN][1000 genomes]
rs2366777	0.80[ASN][1000 genomes]
rs28550273	0.84[ASN][1000 genomes]
rs3087840	0.82[EUR][1000 genomes]
rs4379236	0.84[ASN][1000 genomes]
rs490812	0.88[ASN][1000 genomes]
rs491241	0.91[ASN][1000 genomes]
rs4916681	0.84[ASN][1000 genomes]
rs4916682	0.80[ASN][1000 genomes]
rs4916813	0.80[ASN][1000 genomes]
rs4916814	0.80[ASN][1000 genomes]
rs498491	0.92[ASN][1000 genomes]
rs499148	0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs501640	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs502596	0.89[ASN][1000 genomes]
rs552314	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs558809	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs587818	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs603015	0.84[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs603870	0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs616379	0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs617379	0.90[ASN][1000 genomes]
rs618355	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs623761	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs637442	0.88[ASN][1000 genomes]
rs645652	0.92[ASN][1000 genomes]
rs648430	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs666659	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6878917	0.84[ASN][1000 genomes]
rs6883872	0.84[ASN][1000 genomes]
rs6888355	0.94[ASN][1000 genomes]
rs688956	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs688960	0.92[ASN][1000 genomes]
rs6897910	0.83[EUR][1000 genomes]
rs7716979	0.82[EUR][1000 genomes]
rs7717423	0.84[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7726624	0.87[ASN][1000 genomes]
rs9283788	0.83[ASN][1000 genomes]
rs963866	0.80[ASN][1000 genomes]
rs9790907	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1021142	chr5:89102893-89897826	Active TSS Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
2	nsv537804	chr5:89102893-89897826	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
3	nsv432750	chr5:89410113-90137144	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
4	nsv432751	chr5:89457044-90090444	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
5	nsv529544	chr5:89523963-90412409	Weak transcription Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
6	nsv882365	chr5:89770768-89882618	Flanking Active TSS Genic enhancers Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	13 gene(s)	inside rSNPs	diseases
7	nsv882366	chr5:89826726-89894564	Bivalent/Poised TSS Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
8	nsv933668	chr5:89854253-89999672	Strong transcription Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
9	esv3322073	chr5:89859746-89861794	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
10	esv2582955	chr5:89860131-89861642	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
11	esv3357839	chr5:89860246-89861344	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs474800	LYSMD3	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:89855200-89871000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr5:89859000-89861600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr5:89859400-89864200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr5:89859400-89884200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr5:89859800-89862000	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr5:89860200-89868000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr5:89860400-89862600	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr5:89861000-89861800	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr5:89861000-89862200	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr5:89861200-89861800	Enhancers	iPS-18 Cell Line	embryonic stem cell

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