Variant report

Variant	rs73068742
Chromosome Location	chr19:53493819-53493820
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:61)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:53493775-53493825	Hela-S3	cervix:	n/a
2	chr19:53493775-53493825	AG10803	skin:	n/a
3	chr19:53493775-53493825	RPTEC	kidney:	n/a
4	chr19:53493775-53493825	PrEC	prostate:	n/a
5	chr19:53493775-53493825	AG04449	skin:	fetal
6	chr19:53493775-53493825	GM12878	blood:	n/a
7	chr19:53493775-53493825	Caco-2	colon:	n/a
8	chr19:53493775-53493825	HNPCEpiC	eye:	n/a
9	chr19:53493775-53493825	U87	brain:	n/a
10	chr19:53493775-53493825	NH-A	brain:	n/a
11	chr19:53493775-53493825	NB4	blood:	n/a
12	chr19:53493775-53493825	IMR90	lung:	fetal
13	chr19:53493775-53493825	T-47D	breast:	n/a
14	chr19:53493775-53493825	NT2-D1	testis:	n/a
15	chr19:53493775-53493825	Hepatocyte	liver:	n/a
16	chr19:53493775-53493825	HCT-116	colon:	n/a
17	chr19:53493775-53493825	PFSK-1	brain:	n/a
18	chr19:53493775-53493825	HRCEpiC	kidney:	n/a
19	chr19:53493775-53493825	HL-60	blood:	n/a
20	chr19:53493775-53493825	MCF-7	breast:	n/a
21	chr19:53493775-53493825	MCF10A-Er-Src	breast:	n/a
22	chr19:53493775-53493825	BJ	skin:	n/a
23	chr19:53493775-53493825	HUVEC	blood vessel:	n/a
24	chr19:53493775-53493825	ProgFib	skin:	n/a
25	chr19:53493775-53493825	HEK293	kidney:	embryo
26	chr19:53493775-53493825	AG04450	lung:	fetal
27	chr19:53493775-53493825	K562	blood:	n/a
28	chr19:53493775-53493825	HCPEpiC	choroid plexus:	n/a
29	chr19:53493775-53493825	LNCaP	prostate:	n/a
30	chr19:53493775-53493825	HEEpiC	esophagus:	n/a
31	chr19:53493775-53493825	GM12891	blood:	n/a
32	chr19:53493775-53493825	A549	lung:	n/a
33	chr19:53493775-53493825	GM06990	blood:	n/a
34	chr19:53493775-53493825	SKMC	muscle:	n/a
35	chr19:53493775-53493825	ECC-1	luminal epithelium:	n/a
36	chr19:53493775-53493825	HCF	heart:	n/a
37	chr19:53493775-53493825	HRPEpiC	eye:	n/a
38	chr19:53493775-53493825	HepG2	liver:	n/a
39	chr19:53493775-53493825	AG09309	skin:	n/a
40	chr19:53493775-53493825	GM19239	blood:	n/a
41	chr19:53493775-53493825	HMEC	breast:	n/a
42	chr19:53493775-53493825	HIPEpiC	eye:	n/a
43	chr19:53493775-53493825	Jurkat	blood:	n/a
44	chr19:53493775-53493825	HPAEpiC	pulmonary alveolar:	n/a
45	chr19:53493775-53493825	HCM	heart:	n/a
46	chr19:53493775-53493825	HRE	kidney:	n/a
47	chr19:53493775-53493825	GM12892	blood:	n/a
48	chr19:53493775-53493825	CMK	blood:	n/a
49	chr19:53493775-53493825	SK-N-SH	brain:	n/a
50	chr19:53493775-53493825	H1-hESC	embryonic stem cell:	embryo

No data

Variant related genes	Relation type
ZNF702P	CpG island

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs11669722	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1583962	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1867054	0.85[ASN][1000 genomes]
rs1867055	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs329695	0.86[EUR][1000 genomes]
rs4803031	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4803032	0.84[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs8102809	0.82[AMR][1000 genomes]
rs8102939	0.82[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1066762	chr19:53112568-53552217	Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	nsv432072	chr19:53144788-53554388	Strong transcription ZNF genes & repeats Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
3	nsv1067280	chr19:53193570-53567287	Active TSS Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
4	nsv544062	chr19:53193570-53567287	ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Bivalent Enhancer Genic enhancers 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	33 gene(s)	inside rSNPs	diseases
5	nsv580030	chr19:53194344-53547394	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
6	nsv530807	chr19:53210488-53695881	Strong transcription Active TSS Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
7	esv3326632	chr19:53371248-53697569	Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
8	esv2758506	chr19:53410459-53652575	ZNF genes & repeats Strong transcription Flanking Active TSS Weak transcription Active TSS Genic enhancers Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
9	esv2758769	chr19:53410459-53652575	Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
10	nsv428370	chr19:53410459-53652575	Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
11	esv2757701	chr19:53470514-53554240	Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
12	esv34546	chr19:53478109-53509688	Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
13	nsv817861	chr19:53484032-53505860	Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
14	nsv458753	chr19:53485090-53552296	Strong transcription Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
15	nsv458754	chr19:53485090-53552296	Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
16	nsv580046	chr19:53485090-53552296	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:53467000-53494600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr19:53467200-53495400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr19:53472800-53495800	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr19:53473600-53495800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
5	chr19:53474000-53495800	Weak transcription	Fetal Lung	lung
6	chr19:53481200-53495400	Weak transcription	Fetal Muscle Trunk	muscle
7	chr19:53488200-53495800	Weak transcription	Brain Hippocampus Middle	brain
8	chr19:53489200-53495800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr19:53489800-53494400	Weak transcription	Osteobl	bone
10	chr19:53489800-53495200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr19:53489800-53495800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr19:53490000-53494600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr19:53490000-53495400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr19:53490000-53495800	Weak transcription	Brain Anterior Caudate	brain
15	chr19:53490200-53495200	Weak transcription	Colonic Mucosa	Colon
16	chr19:53490200-53495200	Weak transcription	Gastric	stomach
17	chr19:53490200-53495400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
18	chr19:53490200-53495400	Weak transcription	Fetal Stomach	stomach
19	chr19:53490200-53495400	Weak transcription	Pancreas	Pancrea
20	chr19:53490200-53495400	Weak transcription	Spleen	Spleen
21	chr19:53490200-53495800	Weak transcription	Pancreatic Islets	Pancreatic Islet
22	chr19:53490600-53495200	Weak transcription	Placenta Amnion	Placenta Amnion
23	chr19:53490800-53494600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr19:53490800-53495200	Weak transcription	Colon Smooth Muscle	Colon
25	chr19:53490800-53495200	Weak transcription	Duodenum Mucosa	Duodenum
26	chr19:53490800-53495200	Weak transcription	Stomach Smooth Muscle	stomach
27	chr19:53490800-53495400	Weak transcription	Fetal Intestine Small	intestine
28	chr19:53490800-53495800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr19:53490800-53495800	Weak transcription	Dnd41	blood
30	chr19:53491000-53494400	Weak transcription	NHEK	skin
31	chr19:53491000-53494800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr19:53491000-53495200	Weak transcription	HUES6 Cell Line	embryonic stem cell
33	chr19:53491000-53495200	Weak transcription	Rectal Smooth Muscle	rectum
34	chr19:53491000-53495200	Weak transcription	Right Ventricle	heart
35	chr19:53491000-53495400	Weak transcription	Adipose Nuclei	Adipose
36	chr19:53492200-53495400	Weak transcription	Primary T helper cells fromperipheralblood	blood
37	chr19:53492400-53495400	Weak transcription	Left Ventricle	heart
38	chr19:53492400-53495800	Weak transcription	Primary T helper cells PMA-I stimulated	--
39	chr19:53492600-53494400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr19:53492600-53495200	Weak transcription	Rectal Mucosa Donor 31	rectum
41	chr19:53492800-53494200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr19:53493000-53494600	Weak transcription	Lung	lung
43	chr19:53493000-53495200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr19:53493000-53495400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr19:53493000-53495400	Weak transcription	Ovary	ovary
46	chr19:53493000-53495800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr19:53493000-53495800	Weak transcription	Aorta	Aorta
48	chr19:53493000-53495800	Weak transcription	Fetal Intestine Large	intestine
49	chr19:53493000-53495800	Weak transcription	Sigmoid Colon	Sigmoid Colon
50	chr19:53493200-53494000	Weak transcription	Placenta	Placenta

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