Variant report

Variant	rs934635
Chromosome Location	chr15:51478777-51478778
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:51453641..51456557-chr15:51478131..51480055,2	MCF-7	breast:
2	chr15:51471485..51476477-chr15:51478352..51482224,6	MCF-7	breast:
3	chr15:51470116..51473601-chr15:51476054..51480269,4	K562	blood:
4	chr15:51477370..51478927-chr15:51479650..51482027,2	K562	blood:
5	chr15:51476822..51479125-chr15:51482052..51484475,2	K562	blood:

Extended variants
information (count: 60 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10152435	0.85[ASN][1000 genomes]
rs10468000	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10468001	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11632323	0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12443032	1.00[JPT][hapmap]
rs12591759	0.85[ASN][1000 genomes]
rs12591785	0.85[ASN][1000 genomes]
rs12592286	0.85[ASN][1000 genomes]
rs12594156	0.85[ASN][1000 genomes]
rs12901289	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12901781	0.85[ASN][1000 genomes]
rs12902020	0.85[ASN][1000 genomes]
rs12902455	0.85[ASN][1000 genomes]
rs12911314	1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs1438920	0.85[ASN][1000 genomes]
rs1438922	0.85[ASN][1000 genomes]
rs1438923	0.85[ASN][1000 genomes]
rs1438924	0.85[ASN][1000 genomes]
rs1550334	1.00[ASN][1000 genomes]
rs1550339	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1595584	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17600530	0.81[CEU][hapmap]
rs1866417	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1898738	0.85[ASN][1000 genomes]
rs2414092	0.84[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];0.91[TSI][hapmap];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2414093	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2619684	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2619685	1.00[CHB][hapmap]
rs28757183	1.00[CHB][hapmap]
rs3803369	1.00[CHB][hapmap];0.92[ASN][1000 genomes]
rs4774582	0.85[ASN][1000 genomes]
rs4775912	1.00[CHB][hapmap]
rs4775917	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4775918	0.91[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4775919	0.91[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4775923	0.85[ASN][1000 genomes]
rs4775926	0.85[ASN][1000 genomes]
rs4775928	0.85[ASN][1000 genomes]
rs6493483	0.85[ASN][1000 genomes]
rs6493484	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7170736	1.00[CHB][hapmap];0.83[CHD][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.87[TSI][hapmap];1.00[ASN][1000 genomes]
rs7181680	0.85[ASN][1000 genomes]
rs720316	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72727146	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs732761	1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs732762	1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs7498099	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8027797	0.85[ASN][1000 genomes]
rs8035909	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs893576	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1047443	chr15:50744781-51647023	Strong transcription Active TSS Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
2	nsv569399	chr15:50874964-51562198	Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
3	nsv569400	chr15:50874964-51767265	ZNF genes & repeats Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
4	nsv904214	chr15:51204364-51535192	Strong transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
5	nsv1049644	chr15:51265447-51560445	Strong transcription Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
6	esv34532	chr15:51276128-51752856	Flanking Active TSS Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
7	esv2758382	chr15:51282257-51830339	Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
8	esv2760031	chr15:51282257-51830339	Weak transcription Enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
9	nsv471243	chr15:51345485-52018096	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
10	esv2757600	chr15:51352249-51783981	Weak transcription Bivalent Enhancer Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	21 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs934635	TRPM7	cis	cerebellum	SCAN
rs934635	FGF7	cis	cerebellum	SCAN

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:51474000-51479000	Weak transcription	Right Ventricle	heart
2	chr15:51474800-51479000	Enhancers	Stomach Mucosa	stomach
3	chr15:51475000-51478800	Enhancers	Duodenum Mucosa	Duodenum
4	chr15:51475000-51478800	Enhancers	Fetal Intestine Large	intestine
5	chr15:51475200-51481000	Enhancers	Fetal Heart	heart
6	chr15:51476400-51483000	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr15:51476600-51480400	Enhancers	Fetal Muscle Leg	muscle
8	chr15:51476600-51485600	Weak transcription	Right Atrium	heart
9	chr15:51476800-51479000	Weak transcription	Fetal Muscle Trunk	muscle
10	chr15:51477000-51479400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
11	chr15:51477000-51482200	Weak transcription	HepG2	liver
12	chr15:51477200-51478800	Weak transcription	HSMMtube	muscle
13	chr15:51477200-51479800	Enhancers	Primary B cells from cord blood	blood
14	chr15:51477200-51480400	Weak transcription	Left Ventricle	heart
15	chr15:51477400-51479400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
16	chr15:51477400-51482200	Weak transcription	Lung	lung
17	chr15:51477600-51479400	Enhancers	Brain Hippocampus Middle	brain
18	chr15:51477800-51478800	Enhancers	Brain Substantia Nigra	brain
19	chr15:51478000-51479000	Enhancers	K562	blood
20	chr15:51478000-51479200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr15:51478200-51479200	Enhancers	Brain Cingulate Gyrus	brain
22	chr15:51478200-51479200	Enhancers	Fetal Brain Male	brain
23	chr15:51478200-51480600	Enhancers	Fetal Thymus	thymus
24	chr15:51478400-51478800	Weak transcription	Brain Angular Gyrus	brain
25	chr15:51478400-51479200	Enhancers	Placenta	Placenta
26	chr15:51478400-51480000	Enhancers	Spleen	Spleen
27	chr15:51478400-51483200	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr15:51478600-51479000	Enhancers	Rectal Mucosa Donor 31	rectum
29	chr15:51478600-51479400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr15:51478600-51483400	Weak transcription	Fetal Intestine Small	intestine

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