Variant report

Variant	nsv1066026
Chromosome Location	chr19:36878441-36947928
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr19:36927570-36927771	K562	blood:	n/a	n/a
2	ATF3	chr19:36911828-36912112	K562	blood:	n/a	n/a
3	BACH1	chr19:36909044-36909727	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL3	chr19:36908971-36909895	A549	lung:	n/a	chr19:36909719-36909732 chr19:36909735-36909748
5	BHLHE40	chr19:36909284-36909624	GM12878	blood:	n/a	n/a
6	BHLHE40	chr19:36909422-36909440	K562	blood:	n/a	n/a
7	BHLHE40	chr19:36908676-36908833	K562	blood:	n/a	n/a
8	BHLHE40	chr19:36908569-36908892	GM12878	blood:	n/a	n/a
9	CCNT2	chr19:36909379-36909794	K562	blood:	n/a	n/a
10	CEBPB	chr19:36889252-36889260	A549	lung:	n/a	n/a
11	CEBPB	chr19:36883893-36883897	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr19:36911378-36911546	HepG2	liver:	n/a	chr19:36911403-36911414
13	CEBPD	chr19:36909390-36909667	HepG2	liver:	n/a	n/a
14	CHD1	chr19:36909072-36909157	GM12878	blood:	n/a	n/a
15	CHD2	chr19:36909336-36909689	Hela-S3	cervix:	n/a	n/a
16	CREB1	chr19:36908996-36909752	GM12878	blood:	n/a	n/a
17	CREB1	chr19:36927539-36927776	HepG2	liver:	n/a	n/a
18	CREB1	chr19:36908976-36909834	HepG2	liver:	n/a	n/a
19	CREB1	chr19:36909025-36909766	A549	lung:	n/a	n/a
20	CREB1	chr19:36927452-36927753	H1-hESC	embryonic stem cell:	n/a	n/a
21	CREB1	chr19:36927503-36927869	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr19:36912220-36912370	BJ	skin:	n/a	chr19:36912334-36912352 chr19:36912337-36912346 chr19:36912339-36912349
23	CTCF	chr19:36909700-36909850	GM12864	blood:	n/a	n/a
24	CTCF	chr19:36905140-36905290	A549	lung:	n/a	n/a
25	CTCF	chr19:36909815-36909854	GM12878	blood:	n/a	n/a
26	CTCF	chr19:36909756-36909769	Fibrobl	skin:	n/a	n/a
27	CTCF	chr19:36909786-36909862	GM19238	blood:	n/a	n/a
28	CTCF	chr19:36912240-36912390	HRE	kidney:	n/a	chr19:36912334-36912352 chr19:36912337-36912346 chr19:36912339-36912349
29	CTCF	chr19:36909900-36910050	A549	lung:	n/a	n/a
30	CTCF	chr19:36912280-36912430	HCFaa	heart:	n/a	chr19:36912334-36912352 chr19:36912337-36912346 chr19:36912339-36912349
31	CTCF	chr19:36912300-36912450	HBMEC	blood vessel:	n/a	chr19:36912334-36912352 chr19:36912337-36912346 chr19:36912339-36912349
32	CTCF	chr19:36909100-36909250	HCPEpiC	choroid plexus:	n/a	n/a
33	CTCF	chr19:36909760-36909910	HEK293	kidney:	n/a	n/a
34	CTCF	chr19:36909680-36909830	GM12873	blood:	n/a	n/a
35	CTCF	chr19:36909720-36909870	AG09319	gingival:	n/a	n/a
36	CTCF	chr19:36912220-36912370	HRPEpiC	eye:	n/a	chr19:36912334-36912352 chr19:36912337-36912346 chr19:36912339-36912349
37	CTCF	chr19:36909760-36909910	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr19:36912760-36912848	MCF-7	breast:	n/a	n/a
39	CTCF	chr19:36927520-36927670	Caco-2	colon:	n/a	n/a
40	CTCF	chr19:36912140-36912290	HRE	kidney:	n/a	n/a
41	CTCF	chr19:36912200-36912350	HVMF	connective:	n/a	chr19:36912337-36912346 chr19:36912339-36912349
42	CTCF	chr19:36912180-36912330	HA-sp	spinal cord:	n/a	n/a
43	CTCF	chr19:36909767-36909884	GM12891	blood:	n/a	n/a
44	CTCF	chr19:36912260-36912410	AG09319	gingival:	n/a	chr19:36912334-36912352 chr19:36912337-36912346 chr19:36912339-36912349
45	CTCF	chr19:36912220-36912370	HPF	lung:	n/a	chr19:36912334-36912352 chr19:36912337-36912346 chr19:36912339-36912349
46	CTCF	chr19:36912260-36912410	BJ	skin:	n/a	chr19:36912334-36912352 chr19:36912337-36912346 chr19:36912339-36912349
47	CTCF	chr19:36909680-36909830	NHLF	lung:	n/a	n/a
48	CTCF	chr19:36912289-36912429	H1-hESC	embryonic stem cell:	n/a	chr19:36912334-36912352 chr19:36912337-36912346 chr19:36912339-36912349
49	CTCF	chr19:36912240-36912390	HCPEpiC	choroid plexus:	n/a	chr19:36912334-36912352 chr19:36912337-36912346 chr19:36912339-36912349
50	CTCF	chr19:36909720-36909870	GM12865	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:36909418-36909468	ovcar-3	ovarian:	n/a
2	chr19:36909418-36909468	ovcar-3	ovarian:	n/a
3	chr19:36913451-36913501	HCT-116	colon:	n/a
4	chr19:36912880-36912930	IMR90	lung:	fetal
5	chr19:36909418-36909468	AG10803	skin:	n/a
6	chr19:36910144-36910194	BJ	skin:	n/a
7	chr19:36912702-36912752	T-47D	breast:	n/a
8	chr19:36909831-36909881	U87	brain:	n/a
9	chr19:36913451-36913501	HEK293	kidney:	embryo
10	chr19:36912880-36912930	HEK293	kidney:	embryo
11	chr19:36937832-36937882	HEEpiC	esophagus:	n/a
12	chr19:36912702-36912752	GM19239	blood:	n/a
13	chr19:36912880-36912930	HRCEpiC	kidney:	n/a
14	chr19:36906819-36906869	ECC-1	luminal epithelium:	n/a
15	chr19:36912702-36912752	MCF10A-Er-Src	breast:	n/a
16	chr19:36909913-36909963	SKMC	muscle:	n/a
17	chr19:36913451-36913501	MCF10A-Er-Src	breast:	n/a
18	chr19:36937832-36937882	HCPEpiC	choroid plexus:	n/a
19	chr19:36911014-36911064	HCF	heart:	n/a
20	chr19:36909418-36909468	Hepatocyte	liver:	n/a
21	chr19:36909418-36909468	SK-N-MC	brain:	n/a
22	chr19:36909913-36909963	HCT-116	colon:	n/a
23	chr19:36909326-36909376	IMR90	lung:	fetal
24	chr19:36910144-36910194	NHDF-neo	bronchial:	n/a
25	chr19:36910144-36910194	GM06990	blood:	n/a
26	chr19:36909606-36909656	NHBE	bronchial:	n/a
27	chr19:36883389-36883439	HMEC	breast:	n/a
28	chr19:36915447-36915497	AG04449	skin:	fetal
29	chr19:36909831-36909881	GM12892	blood:	n/a
30	chr19:36891345-36891395	ovcar-3	ovarian:	n/a
31	chr19:36937832-36937882	NT2-D1	testis:	n/a
32	chr19:36911014-36911064	SAEC	small airway:	n/a
33	chr19:36915447-36915497	NT2-D1	testis:	n/a
34	chr19:36909913-36909963	MCF-7	breast:	n/a
35	chr19:36910144-36910194	HL-60	blood:	n/a
36	chr19:36906819-36906869	Hepatocyte	liver:	n/a
37	chr19:36913451-36913501	AoSMC	blood vessel:	n/a
38	chr19:36913451-36913501	HPAEpiC	pulmonary alveolar:	n/a
39	chr19:36891345-36891395	AG09319	gingival:	n/a
40	chr19:36906819-36906869	Hela-S3	cervix:	n/a
41	chr19:36910116-36910166	AG04450	lung:	fetal
42	chr19:36915447-36915497	SK-N-MC	brain:	n/a
43	chr19:36912880-36912930	HMEC	breast:	n/a
44	chr19:36883389-36883439	T-47D	breast:	n/a
45	chr19:36891345-36891395	HCPEpiC	choroid plexus:	n/a
46	chr19:36913451-36913501	Jurkat	blood:	n/a
47	chr19:36909913-36909963	HAEpiC	amniotic membrane:	n/a
48	chr19:36906819-36906869	SK-N-SH	brain:	n/a
49	chr19:36915447-36915497	LNCaP	prostate:	n/a
50	chr19:36891345-36891395	MCF-7	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:36884346..36886585-chr19:36904076..36906046,2	MCF-7	breast:
2	chr19:36884346..36886585-chr19:36904076..36906046,2	MCF-7	breast:
3	chr19:36944101..36946636-chr19:36951837..36953729,2	K562	blood:
4	chr19:36921260..36923762-chr19:37063794..37066625,2	K562	blood:
5	chr19:36940091..36943076-chr19:37061156..37065481,3	K562	blood:
6	chr19:36895506..36897062-chr19:36899280..36901611,2	K562	blood:
7	chr19:36924487..36927399-chr19:37259800..37262103,2	K562	blood:
8	chr19:36869440..36871564-chr19:36878209..36879781,2	MCF-7	breast:
9	chr19:36909374..36910931-chr19:36934594..36936776,2	K562	blood:

Variant related genes	Relation type
ZNF566	TF binding region
ENSG00000267142	TF binding region
ZFP82	TF binding region
ZNF566	CpG island
ENSG00000267142	CpG island
ZFP82	CpG island
ENSG00000142065	chromatin interactions
ENSG00000186020	chromatin interactions
ENSG00000181007	chromatin interactions
ENSG00000233527	chromatin interactions

Extended variants
information (count: 2020 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:2020 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370103952	chr19:36878463-36878464	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs536185276	chr19:36878476-36878477	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs542641678	chr19:36878479-36878480	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs554566397	chr19:36878480-36878481	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs2967514	chr19:36878517-36878518	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs2945959	chr19:36878564-36878565	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs147129498	chr19:36878582-36878583	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs565333949	chr19:36878665-36878666	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs532643169	chr19:36878666-36878667	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs541601298	chr19:36878707-36878708	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs4425007	chr19:36878763-36878764	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs371020532	chr19:36878902-36878903	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs530394029	chr19:36878911-36878912	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs548870470	chr19:36878914-36878915	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs567282025	chr19:36878916-36878917	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs531287607	chr19:36879072-36879073	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs566307668	chr19:36879104-36879105	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs144277606	chr19:36879141-36879142	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs189898409	chr19:36879146-36879147	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs182535750	chr19:36879152-36879153	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs188396642	chr19:36879173-36879174	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs374301809	chr19:36879270-36879271	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs553910659	chr19:36879503-36879504	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs540049551	chr19:36879504-36879505	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs549365735	chr19:36879532-36879533	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs191087388	chr19:36879589-36879590	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs183139926	chr19:36879655-36879656	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs554400933	chr19:36879658-36879659	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs187545506	chr19:36879670-36879671	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs576030219	chr19:36879685-36879686	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs57098713	chr19:36879701-36879702	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs558337038	chr19:36879746-36879747	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs191968523	chr19:36879769-36879770	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs577250473	chr19:36879830-36879831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs576324362	chr19:36879895-36879896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs541290646	chr19:36879937-36879938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs34929021	chr19:36879946-36879947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs397859200	chr19:36879960-36879961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs78377900	chr19:36879961-36879962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs560007970	chr19:36879973-36879974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs575048550	chr19:36880003-36880004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs542545785	chr19:36880045-36880046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs12975337	chr19:36880087-36880088	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs531250997	chr19:36880127-36880128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs549736096	chr19:36880209-36880210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs537398637	chr19:36880232-36880233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs141036317	chr19:36880309-36880310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs556171557	chr19:36880331-36880332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs199771474	chr19:36880400-36880401	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs185101823	chr19:36880408-36880409	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21858162	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
renal disease	20603712	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Ovarian cancer	21397856	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Ovarian cancer	20844748	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cancer	21183584	CNVD
Honadal dysgenesis	21048976	CNVD
Neurodevelopmental disorder	22521361	CNVD
Endometrial cancer	23636398	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Invasive pancreatic ductal carcinoma	18765526	CNVD
Rhabdomyosarcoma	16790082	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Glioma	17123091	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:2003 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:36870600-36880400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr19:36870600-36880600	Weak transcription	Ovary	ovary
3	chr19:36870800-36882400	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr19:36877000-36883000	Weak transcription	Brain Angular Gyrus	brain
5	chr19:36878200-36880400	Weak transcription	Dnd41	blood
6	chr19:36878200-36882800	Weak transcription	Fetal Heart	heart
7	chr19:36878400-36880400	Weak transcription	Brain Germinal Matrix	brain
8	chr19:36878400-36880600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr19:36878600-36883000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr19:36880200-36880400	Weak transcription	Fetal Brain Male	brain
11	chr19:36880400-36881000	ZNF genes & repeats	Fetal Brain Male	brain
12	chr19:36880400-36881200	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr19:36880400-36881200	ZNF genes & repeats	Dnd41	blood
14	chr19:36880400-36887400	ZNF genes & repeats	Brain Germinal Matrix	brain
15	chr19:36880400-36892800	ZNF genes & repeats	Liver	Liver
16	chr19:36880400-36893200	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr19:36880400-36904600	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr19:36880600-36881000	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr19:36880600-36881200	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr19:36880600-36881200	ZNF genes & repeats	Duodenum Mucosa	Duodenum
21	chr19:36880600-36882800	Weak transcription	Brain Substantia Nigra	brain
22	chr19:36880600-36886600	ZNF genes & repeats	Adipose Nuclei	Adipose
23	chr19:36880600-36889000	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
24	chr19:36880600-36893000	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood
25	chr19:36880600-36893200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr19:36880800-36881200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr19:36880800-36881200	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon
28	chr19:36880800-36886600	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
29	chr19:36880800-36888400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr19:36881000-36881200	ZNF genes & repeats	Primary T killer naive cells fromperipheralblood	blood
31	chr19:36881000-36883000	Weak transcription	Fetal Brain Male	brain
32	chr19:36881000-36886600	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
33	chr19:36881200-36882400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr19:36881200-36882400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr19:36881200-36882400	Weak transcription	Dnd41	blood
36	chr19:36881200-36882800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr19:36881200-36883000	Weak transcription	Placenta Amnion	Placenta Amnion
38	chr19:36881400-36892800	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr19:36882000-36887400	ZNF genes & repeats	A549	lung
40	chr19:36882000-36891800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
41	chr19:36882200-36883400	ZNF genes & repeats	Fetal Stomach	stomach
42	chr19:36882200-36886200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr19:36882200-36886600	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
44	chr19:36882200-36886600	ZNF genes & repeats	Psoas Muscle	Psoas
45	chr19:36882200-36886800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
46	chr19:36882200-36888800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
47	chr19:36882200-36890400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
48	chr19:36882200-36892800	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
49	chr19:36882200-36908800	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr19:36882400-36883000	Strong transcription	Dnd41	blood

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