Variant report

Variant	rs10419765
Chromosome Location	chr19:52818402-52818403
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	chr19:52799239..52802011-chr19:52817590..52819233,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000198464	Chromatin interaction
ENSG00000269102	Chromatin interaction

Extended variants
information (count: 58 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10404965	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10405321	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10407594	0.84[AFR][1000 genomes];0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10408636	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10411053	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10415728	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11084147	0.84[EUR][1000 genomes]
rs11084148	0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11667008	0.84[EUR][1000 genomes]
rs12462904	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12462953	0.96[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1540745	0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs167707	0.95[JPT][hapmap];0.84[ASN][1000 genomes]
rs167708	0.84[ASN][1000 genomes]
rs170414	0.91[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.91[ASN][1000 genomes]
rs1810006	0.89[ASN][1000 genomes]
rs2115075	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2115076	0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2657933	0.88[ASN][1000 genomes]
rs321902	0.86[ASN][1000 genomes]
rs321919	0.86[CHB][hapmap];0.95[JPT][hapmap];0.84[ASN][1000 genomes]
rs321921	0.91[CEU][hapmap];0.90[CHB][hapmap];0.95[JPT][hapmap];0.92[ASN][1000 genomes]
rs321922	0.91[ASN][1000 genomes]
rs321923	0.92[ASN][1000 genomes]
rs321924	0.89[ASN][1000 genomes]
rs321925	0.91[ASN][1000 genomes]
rs321926	0.95[JPT][hapmap];0.84[ASN][1000 genomes]
rs321928	0.83[ASN][1000 genomes]
rs321930	0.88[YRI][hapmap]
rs321932	0.83[ASN][1000 genomes]
rs321934	0.82[ASN][1000 genomes]
rs321935	0.84[JPT][hapmap];0.83[ASN][1000 genomes]
rs4801912	1.00[CEU][hapmap];0.95[CHB][hapmap];0.82[YRI][hapmap];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4802920	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7247178	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7249338	0.86[ASN][1000 genomes]
rs7249784	0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7256570	0.92[ASN][1000 genomes]
rs7258711	0.90[ASN][1000 genomes]
rs7260178	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs8102373	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8109096	0.95[CEU][hapmap];0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs8109646	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs8112051	0.95[CEU][hapmap];0.82[CHB][hapmap];0.90[JPT][hapmap];0.88[EUR][1000 genomes]
rs8112337	0.91[CEU][hapmap];0.84[EUR][1000 genomes]
rs8113784	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs890842	0.89[JPT][hapmap]
rs890843	0.87[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	nsv1065410	chr19:52103914-52889530	Genic enhancers Enhancers ZNF genes & repeats Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	596 gene(s)	inside rSNPs	diseases
2	esv3366000	chr19:52491073-52842946	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
3	nsv1066015	chr19:52502213-52890308	Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
4	nsv544059	chr19:52502213-52890308	Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
5	nsv833873	chr19:52788939-52937281	Weak transcription Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
6	nsv1066537	chr19:52794424-53044977	Active TSS ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
7	nsv544060	chr19:52794424-53044977	ZNF genes & repeats Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
8	nsv912299	chr19:52795985-52832830	ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	n/a
9	nsv458742	chr19:52808986-52866171	Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	n/a
10	nsv580008	chr19:52808986-52866171	ZNF genes & repeats Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	n/a

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10419765	ZNF480	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:52801800-52827200	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr19:52801800-52829200	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr19:52802000-52826400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr19:52802000-52830000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr19:52802200-52827400	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
6	chr19:52802200-52828400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr19:52802200-52829200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
8	chr19:52802400-52828800	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
9	chr19:52802400-52841800	ZNF genes & repeats	Liver	Liver
10	chr19:52802600-52826800	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
11	chr19:52802600-52827600	ZNF genes & repeats	Dnd41	blood
12	chr19:52803800-52829000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
13	chr19:52803800-52829200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
14	chr19:52804400-52827200	ZNF genes & repeats	Primary B cells from peripheral blood	blood
15	chr19:52805000-52819000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
16	chr19:52805200-52829000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
17	chr19:52805400-52829200	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr19:52805600-52827800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr19:52807400-52824400	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
20	chr19:52807400-52824800	ZNF genes & repeats	Primary Natural Killer cells fromperipheralblood	blood
21	chr19:52807800-52827000	ZNF genes & repeats	Primary hematopoietic stem cells	blood
22	chr19:52808000-52824200	ZNF genes & repeats	Fetal Intestine Small	intestine
23	chr19:52808200-52826200	ZNF genes & repeats	Thymus	Thymus
24	chr19:52808200-52827200	ZNF genes & repeats	Left Ventricle	heart
25	chr19:52808200-52831800	ZNF genes & repeats	Duodenum Mucosa	Duodenum
26	chr19:52808400-52826200	ZNF genes & repeats	Placenta	Placenta
27	chr19:52808400-52826600	ZNF genes & repeats	Fetal Muscle Leg	muscle
28	chr19:52808400-52827200	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr19:52808600-52824400	ZNF genes & repeats	Fetal Stomach	stomach
30	chr19:52808600-52828000	ZNF genes & repeats	Fetal Lung	lung
31	chr19:52809200-52829800	ZNF genes & repeats	Primary T cells from cord blood	blood
32	chr19:52810600-52826400	ZNF genes & repeats	Fetal Intestine Large	intestine
33	chr19:52811000-52826400	ZNF genes & repeats	Primary T cells fromperipheralblood	blood
34	chr19:52813000-52818800	Weak transcription	Brain Anterior Caudate	brain
35	chr19:52813000-52818800	Weak transcription	Brain Cingulate Gyrus	brain
36	chr19:52813000-52819000	Weak transcription	Osteobl	bone
37	chr19:52813000-52819600	Weak transcription	HUVEC	blood vessel
38	chr19:52813200-52818800	Weak transcription	NHDF-Ad	bronchial
39	chr19:52814400-52826200	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon
40	chr19:52814400-52827400	ZNF genes & repeats	Primary B cells from cord blood	blood
41	chr19:52814600-52824200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr19:52814600-52826800	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
43	chr19:52814600-52829400	ZNF genes & repeats	Colon Smooth Muscle	Colon
44	chr19:52814600-52836600	ZNF genes & repeats	Adipose Nuclei	Adipose
45	chr19:52814800-52819600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr19:52814800-52822400	Strong transcription	K562	blood
47	chr19:52814800-52826200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr19:52814800-52826600	ZNF genes & repeats	Primary T killer naive cells fromperipheralblood	blood
49	chr19:52814800-52827800	ZNF genes & repeats	Rectal Mucosa Donor 29	rectum
50	chr19:52814800-52828000	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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