Variant report

Variant	rs4699770
Chromosome Location	chr4:100985201-100985202
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:100871002..100872693-chr4:100984695..100986300,2	K562	blood:
2	chr4:100985133..100987017-chr4:100990032..100992836,2	K562	blood:

Variant related genes	Relation type
ENSG00000164032	Chromatin interaction
ENSG00000245322	Chromatin interaction

Extended variants
information (count: 28 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10029894	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11729426	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11732283	0.92[CEU][hapmap];0.95[CHB][hapmap];0.94[JPT][hapmap];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12649983	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4128310	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4235442	0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4593140	0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4635824	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4699389	0.95[CHB][hapmap];0.95[CHD][hapmap];0.93[GIH][hapmap];0.89[JPT][hapmap];0.88[LWK][hapmap];0.94[MEX][hapmap];0.87[MKK][hapmap];0.84[TSI][hapmap];0.92[AMR][1000 genomes];0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4699390	0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4699391	0.83[ASN][1000 genomes]
rs4699392	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4699773	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4699774	0.83[CEU][hapmap];0.89[JPT][hapmap]
rs55705206	1.00[ASN][1000 genomes]
rs61294522	0.80[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs62306122	1.00[ASN][1000 genomes]
rs62306150	0.82[EUR][1000 genomes]
rs6532843	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6834862	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6837281	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6840267	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6856293	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7671736	0.88[CEU][hapmap];0.81[CHD][hapmap];0.89[JPT][hapmap];0.80[EUR][1000 genomes]
rs7697932	0.95[ASN][1000 genomes]
rs7698869	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv427689	chr4:100931741-101216531	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv830018	chr4:100977238-101027920	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:5)

SNP	Gene	Cis/trans	Tissue	Source
rs4699770	C4orf37	cis	cerebellum	SCAN
rs4699770	DNAJB14	cis	parietal	SCAN
rs4699770	RAP1GDS1	cis	parietal	SCAN
rs4699770	DDIT4L	cis	lymphoblastoid	seeQTL
rs4699770	MAPKSP1	cis	parietal	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:100983200-100985400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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