Variant report

Variant	rs7253637
Chromosome Location	chr19:52018717-52018718
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:6)
CpG islands
(count:0)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:6 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr19:52018580-52018730	AG09319	gingival:	n/a	n/a
2	CTCF	chr19:52018680-52018830	GM06990	blood:	n/a	n/a
3	CTCF	chr19:52017778-52018755	A549	lung:	n/a	n/a
4	CTCF	chr19:52018065-52018733	SK-N-SH	brain:	n/a	n/a
5	CTCF	chr19:52018599-52018733	Spleen_OC	spleen:	n/a	n/a
6	CTCF	chr19:52018066-52018734	K562	blood:	n/a	n/a

No data

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:51976116..51976755-chr19:52018185..52018795,2	MCF-7	breast:
2	chr19:52016872..52019391-chr19:52020928..52022569,2	K562	blood:
3	chr19:52017645..52019212-chr19:52145235..52147486,2	MCF-7	breast:
4	chr19:51975937..51976795-chr19:52018276..52018797,2	MCF-7	breast:
5	chr19:52017775..52020070-chr19:52020928..52023359,4	K562	blood:

No data

Variant related genes	Relation type
ENSG00000268777	TF binding region
ENSG00000268777	Chromatin interaction

Extended variants
information (count: 35 )
Associated
traits (count: 11 )

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10405214	0.83[CHB][hapmap];0.83[CHD][hapmap];0.82[GIH][hapmap]
rs10407110	0.81[ASW][hapmap]
rs10853836	0.84[CEU][hapmap];0.83[EUR][1000 genomes]
rs1160392	0.81[EUR][1000 genomes]
rs1457098	0.93[ASW][hapmap];0.81[CEU][hapmap]
rs1551556	0.84[CEU][hapmap];0.81[TSI][hapmap];0.81[EUR][1000 genomes]
rs1551559	0.81[CEU][hapmap]
rs2124910	0.87[ASW][hapmap];0.81[CEU][hapmap]
rs2168643	0.84[CEU][hapmap];0.94[GIH][hapmap];0.88[TSI][hapmap];0.85[EUR][1000 genomes]
rs2305772	0.83[CEU][hapmap]
rs2864101	0.81[EUR][1000 genomes]
rs2864102	1.00[CEU][hapmap];0.83[CHB][hapmap];0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2864103	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2864104	1.00[CEU][hapmap];0.83[CHB][hapmap];0.83[CHD][hapmap];0.97[GIH][hapmap];0.97[TSI][hapmap];0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs3810110	0.81[TSI][hapmap]
rs3829658	0.80[CHD][hapmap];0.92[TSI][hapmap];0.85[EUR][1000 genomes]
rs3976745	1.00[CEU][hapmap];0.82[CHB][hapmap];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4146202	0.81[CEU][hapmap]
rs4801873	1.00[CEU][hapmap];0.85[CHB][hapmap];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4801874	0.93[ASW][hapmap];0.94[GIH][hapmap];0.83[MKK][hapmap];0.88[TSI][hapmap];0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4802800	0.81[CEU][hapmap]
rs4802807	0.87[ASW][hapmap];0.81[CEU][hapmap]
rs7255948	0.81[CEU][hapmap];0.81[EUR][1000 genomes]
rs8101241	0.83[ASN][1000 genomes]
rs8102707	0.84[CEU][hapmap];0.81[TSI][hapmap];0.81[EUR][1000 genomes]
rs8182477	0.83[CHB][hapmap];0.81[CHD][hapmap]
rs897783	0.81[CEU][hapmap]
rs9304718	0.84[CEU][hapmap];0.81[TSI][hapmap];0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1066308	chr19:51680133-52103974	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
2	nsv544049	chr19:51680133-52103974	Bivalent Enhancer Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
3	nsv544051	chr19:51944903-52147459	Bivalent Enhancer Strong transcription Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
4	esv2758504	chr19:51991896-52266700	Enhancers Strong transcription Transcr. at gene 5' and 3' Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	542 gene(s)	inside rSNPs	diseases
5	esv2758767	chr19:51991896-52604625	Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	578 gene(s)	inside rSNPs	diseases
6	nsv469584	chr19:52001381-52151821	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
7	nsv482654	chr19:52001381-52151821	Enhancers Strong transcription Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases

mRNA abundance (count:11)

SNP	Gene	Cis/trans	Tissue	Source
rs7253637	PPP1R12C	cis	cerebellum	SCAN
rs7253637	SIGLEC12	cis	Thyroid	GTEx
rs7253637	SIGLEC12	cis	lung	GTEx
rs7253637	SIGLEC12	cis	Artery Aorta	GTEx
rs7253637	SIGLEC12	cis	Adipose Subcutaneous	GTEx
rs7253637	SIGLEC12	cis	multi-tissue	Pritchard
rs7253637	ZNF468	cis	cerebellum	SCAN
rs7253637	ZNF584	cis	parietal	SCAN
rs7253637	SIGLEC12	cis	Skin Sun Exposed Lower leg	GTEx
rs7253637	SIGLEC12	cis	Artery Tibial	GTEx
rs7253637	SIGLEC12	cis	Whole Blood	GTEx

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:52017400-52018800	Enhancers	K562	blood
2	chr19:52018400-52021400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr19:52018600-52021200	Weak transcription	Primary B cells from peripheral blood	blood

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