Variant report

Variant	rs1673381
Chromosome Location	chr5:89908521-89908522
allele	A/C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

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

No.	Distal block	Cell Line	Cell type
1	chr5:89825899..89828736-chr5:89905925..89909224,3	K562	blood:
2	chr5:89824868..89827169-chr5:89907732..89909501,2	K562	blood:
3	chr5:89908105..89911531-chr5:89917925..89920470,3	K562	blood:
4	chr5:89903854..89914063-chr5:89934543..89943749,18	K562	blood:
5	chr5:89908130..89913352-chr5:89914891..89917115,4	K562	blood:
6	chr5:89904971..89912478-chr5:89936195..89941599,10	K562	blood:
7	chr5:89904239..89908604-chr5:89932898..89936068,3	K562	blood:
8	chr5:89908014..89909686-chr5:89928163..89930208,2	K562	blood:
9	chr5:89908142..89911258-chr5:89951635..89955571,4	K562	blood:
10	chr5:89908014..89912492-chr5:89923558..89929663,6	K562	blood:

No data

Variant related genes	Relation type
ENSG00000164199	Chromatin interaction
ENSG00000176018	Chromatin interaction

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10043564	1.00[CEU][hapmap];0.83[JPT][hapmap];0.87[EUR][1000 genomes]
rs10064606	0.84[JPT][hapmap]
rs11958484	0.83[JPT][hapmap]
rs12186867	1.00[CEU][hapmap];0.83[JPT][hapmap];0.88[EUR][1000 genomes]
rs12653924	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1316970	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs1474119	1.00[CEU][hapmap]
rs149321	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs154566	0.94[ASN][1000 genomes]
rs154569	0.86[JPT][hapmap]
rs2366772	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2366775	1.00[CEU][hapmap];0.95[CHB][hapmap];0.96[JPT][hapmap];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs250366	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs250369	0.94[ASN][1000 genomes]
rs250377	0.82[JPT][hapmap]
rs257847	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs27196	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs27197	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs27201	0.81[JPT][hapmap]
rs28480058	0.90[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs3112773	0.99[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs42467	0.86[JPT][hapmap]
rs4588621	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs5028525	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs511393	0.81[JPT][hapmap]
rs567441	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs599432	1.00[JPT][hapmap]
rs649449	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs656679	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs6891287	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs6891840	0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6892132	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs908818	1.00[CEU][hapmap];0.83[JPT][hapmap];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9283789	0.92[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	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
2	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
3	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
4	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
5	nsv531965	chr5:89886550-90145002	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:89892800-89909000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr5:89902600-89917400	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr5:89906400-89908600	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr5:89906400-89908600	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chr5:89907000-89908600	Enhancers	Fetal Brain Male	brain
6	chr5:89907000-89909000	Weak transcription	Fetal Brain Female	brain
7	chr5:89907400-89911000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr5:89907800-89909800	Enhancers	H9 Cell Line	embryonic stem cell
9	chr5:89907800-89910200	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr5:89908000-89908800	Weak transcription	Brain Germinal Matrix	brain
11	chr5:89908200-89908600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr5:89908200-89908600	Enhancers	GM12878-XiMat	blood
13	chr5:89908200-89909400	Enhancers	Brain Cingulate Gyrus	brain
14	chr5:89908200-89910200	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr5:89908200-89910600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr5:89908400-89908600	Enhancers	K562	blood
17	chr5:89908400-89909400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr5:89908400-89909800	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr5:89908400-89910000	Enhancers	ES-I3 Cell Line	embryonic stem cell

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