Variant report

Variant	rs10403464
Chromosome Location	chr19:52731572-52731573
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:5)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

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

No.	Distal block	Cell Line	Cell type
1	chr19:52692286..52695844-chr19:52730833..52733280,4	MCF-7	breast:
2	chr19:52709631..52712129-chr19:52729656..52731766,2	K562	blood:
3	chr19:52729294..52731745-chr19:52733728..52736349,4	MCF-7	breast:
4	chr19:52730627..52732883-chr19:52789456..52792184,2	K562	blood:
5	chr19:52731463..52733004-chr19:52746080..52748191,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF836-2	chr19:52731496-52731862	ENSG00000268015.1

No data

Variant related genes	Relation type
ENSG00000268015	Chromatin interaction
ENSG00000105568	Chromatin interaction

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10403202	0.98[EUR][1000 genomes]
rs10403283	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10403311	0.92[EUR][1000 genomes]
rs10407063	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10407502	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10408119	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10411211	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10412110	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10413012	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10413435	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10414083	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10414197	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10414423	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10414536	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10416785	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10417033	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10417253	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10421440	0.98[EUR][1000 genomes]
rs10421589	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10422483	0.98[EUR][1000 genomes]
rs10422838	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10423125	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10426002	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10426786	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16983603	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16983610	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17835942	0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2115074	1.00[EUR][1000 genomes]
rs55751302	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55871532	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57102373	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60063830	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7255058	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7256216	0.98[EUR][1000 genomes]
rs73935053	0.89[EUR][1000 genomes]
rs8100048	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs8100600	0.98[EUR][1000 genomes]
rs8101990	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs8106271	0.98[EUR][1000 genomes]
rs874421	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 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

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:52694600-52732800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr19:52695400-52732200	Strong transcription	Fetal Lung	lung
3	chr19:52695400-52733200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
4	chr19:52696000-52732200	Strong transcription	Monocytes-CD14+_RO01746	blood
5	chr19:52696000-52732400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr19:52696000-52733000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr19:52696200-52732400	Strong transcription	HUES6 Cell Line	embryonic stem cell
8	chr19:52696200-52732400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
9	chr19:52696200-52732400	Strong transcription	Primary B cells from cord blood	blood
10	chr19:52697600-52732400	Strong transcription	Sigmoid Colon	Sigmoid Colon
11	chr19:52697600-52733200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
12	chr19:52697800-52732200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr19:52697800-52732400	Strong transcription	HUES64 Cell Line	embryonic stem cell
14	chr19:52697800-52732400	Strong transcription	Rectal Mucosa Donor 29	rectum
15	chr19:52697800-52732600	Strong transcription	Primary T cells from cord blood	blood
16	chr19:52697800-52733000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr19:52698000-52732200	Strong transcription	Rectal Mucosa Donor 31	rectum
18	chr19:52698000-52732200	Strong transcription	Dnd41	blood
19	chr19:52698200-52732000	Strong transcription	GM12878-XiMat	blood
20	chr19:52698200-52732400	Strong transcription	HUES48 Cell Line	embryonic stem cell
21	chr19:52698200-52732400	Strong transcription	HepG2	liver
22	chr19:52698200-52732600	Strong transcription	Fetal Brain Female	brain
23	chr19:52698400-52732400	Strong transcription	Fetal Thymus	thymus
24	chr19:52698600-52732000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
25	chr19:52698800-52732400	Strong transcription	Liver	Liver
26	chr19:52700800-52732200	Strong transcription	Primary T helper cells fromperipheralblood	blood
27	chr19:52702200-52731800	Strong transcription	Primary B cells from peripheral blood	blood
28	chr19:52702200-52732200	Strong transcription	H1 Cell Line	embryonic stem cell
29	chr19:52702600-52732200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
30	chr19:52703000-52731600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr19:52703000-52732600	Strong transcription	Primary neutrophils fromperipheralblood	blood
32	chr19:52703000-52734600	Strong transcription	Fetal Stomach	stomach
33	chr19:52703200-52732200	Strong transcription	Cortex derived primary cultured neurospheres	brain
34	chr19:52703200-52732400	Strong transcription	H9 Cell Line	embryonic stem cell
35	chr19:52703200-52732400	Strong transcription	Primary monocytes fromperipheralblood	blood
36	chr19:52703200-52732800	Strong transcription	Brain Germinal Matrix	brain
37	chr19:52703200-52733200	Strong transcription	Duodenum Mucosa	Duodenum
38	chr19:52703200-52734000	Strong transcription	Lung	lung
39	chr19:52703600-52733200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr19:52703800-52732200	Strong transcription	NHEK	skin
41	chr19:52703800-52733200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr19:52704000-52732200	Strong transcription	Primary T helper cells PMA-I stimulated	--
43	chr19:52704000-52732400	Strong transcription	Brain Cingulate Gyrus	brain
44	chr19:52704000-52733200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr19:52704200-52731800	Strong transcription	HUVEC	blood vessel
46	chr19:52704200-52732000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr19:52704200-52732400	Strong transcription	NHLF	lung
48	chr19:52704400-52732400	Strong transcription	Muscle Satellite Cultured Cells	--
49	chr19:52704400-52732400	Strong transcription	Adipose Nuclei	Adipose
50	chr19:52704400-52733000	Strong transcription	Colonic Mucosa	Colon

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