Variant report

Variant	nsv902056
Chromosome Location	chr14:67261821-67308900
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	BACH1	chr14:67305949-67305970	K562	blood:	n/a	n/a
2	BRCA1	chr14:67288110-67288222	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr14:67290366-67290605	A549	lung:	n/a	n/a
4	CEBPB	chr14:67280301-67280681	K562	blood:	n/a	chr14:67280486-67280497
5	CEBPB	chr14:67280308-67280682	HepG2	liver:	n/a	chr14:67280486-67280497
6	CEBPB	chr14:67280297-67280677	A549	lung:	n/a	chr14:67280486-67280497
7	CEBPB	chr14:67280214-67280811	MCF-7	breast:	n/a	chr14:67280486-67280497
8	CEBPB	chr14:67280360-67280549	HepG2	liver:	n/a	chr14:67280486-67280497
9	CEBPB	chr14:67280307-67280679	Hela-S3	cervix:	n/a	chr14:67280486-67280497
10	CEBPB	chr14:67280306-67280665	H1-hESC	embryonic stem cell:	n/a	chr14:67280486-67280497
11	CEBPB	chr14:67280292-67280682	HepG2	liver:	n/a	chr14:67280486-67280497
12	CEBPB	chr14:67280182-67280792	A549	lung:	n/a	chr14:67280486-67280497
13	CEBPB	chr14:67280298-67280687	IMR90	lung:	n/a	chr14:67280486-67280497
14	CEBPB	chr14:67280291-67280680	ECC-1	luminal epithelium:	n/a	chr14:67280486-67280497
15	CEBPB	chr14:67280194-67280806	MCF-7	breast:	n/a	chr14:67280486-67280497
16	CEBPB	chr14:67290364-67290658	IMR90	lung:	n/a	n/a
17	CEBPB	chr14:67280318-67280671	ECC-1	luminal epithelium:	n/a	chr14:67280486-67280497
18	CEBPB	chr14:67280261-67280604	HepG2	liver:	n/a	chr14:67280486-67280497
19	CEBPB	chr14:67280274-67280662	A549	lung:	n/a	chr14:67280486-67280497
20	CTCF	chr14:67268780-67268930	HepG2	liver:	n/a	n/a
21	CTCF	chr14:67291160-67291310	HEEpiC	esophagus:	n/a	n/a
22	CTCF	chr14:67298860-67299010	HCFaa	heart:	n/a	n/a
23	CTCF	chr14:67268755-67268820	GM20000	blood:	n/a	n/a
24	CTCF	chr14:67295888-67295970	GM13976	blood:	n/a	n/a
25	CTCF	chr14:67291163-67291337	HUVEC	blood vessel:	n/a	n/a
26	CTCF	chr14:67280631-67280687	MCF-7	breast:	n/a	n/a
27	E2F4	chr14:67283065-67283200	MCF10A-Er-Src	breast:	n/a	n/a
28	EBF1	chr14:67294101-67294102	GM12878	blood:	n/a	n/a
29	FOSL2	chr14:67297114-67297382	SK-N-SH	brain:	n/a	n/a
30	GATA3	chr14:67297018-67297613	SK-N-SH	brain:	n/a	n/a
31	GATA3	chr14:67276404-67276599	SH-SY5Y	brain:	n/a	n/a
32	GATA3	chr14:67307457-67307609	SH-SY5Y	brain:	n/a	n/a
33	GATA3	chr14:67296926-67297586	SK-N-SH	brain:	n/a	n/a
34	KAP1	chr14:67282395-67282884	HEK293	kidney:	n/a	n/a
35	MAFF	chr14:67298011-67298231	HepG2	liver:	n/a	chr14:67298093-67298107 chr14:67298087-67298105
36	MAFF	chr14:67298069-67298198	K562	blood:	n/a	chr14:67298093-67298107 chr14:67298087-67298105
37	MAFK	chr14:67297973-67298218	IMR90	lung:	n/a	chr14:67298090-67298110 chr14:67298089-67298104 chr14:67298092-67298108 chr14:67298089-67298105 chr14:67298088-67298102
38	MAFK	chr14:67298014-67298122	K562	blood:	n/a	chr14:67298090-67298110 chr14:67298089-67298104 chr14:67298092-67298108 chr14:67298089-67298105 chr14:67298088-67298102
39	MAFK	chr14:67298006-67298212	HepG2	liver:	n/a	chr14:67298090-67298110 chr14:67298089-67298104 chr14:67298092-67298108 chr14:67298089-67298105 chr14:67298088-67298102
40	MAFK	chr14:67297939-67298258	HepG2	liver:	n/a	chr14:67298090-67298110 chr14:67298089-67298104 chr14:67298092-67298108 chr14:67298089-67298105 chr14:67298088-67298102
41	MAFK	chr14:67297961-67298247	Hela-S3	cervix:	n/a	chr14:67298090-67298110 chr14:67298089-67298104 chr14:67298092-67298108 chr14:67298089-67298105 chr14:67298088-67298102
42	MYC	chr14:67268412-67268448	MCF-7	breast:	n/a	n/a
43	MYC	chr14:67280789-67280817	MCF-7	breast:	n/a	n/a
44	MYC	chr14:67280814-67280884	MCF-7	breast:	n/a	n/a
45	MYC	chr14:67269945-67269995	MCF-7	breast:	n/a	n/a
46	MYC	chr14:67268550-67268570	MCF-7	breast:	n/a	n/a
47	MYC	chr14:67280798-67280803	MCF-7	breast:	n/a	n/a
48	MYC	chr14:67280654-67280775	MCF-7	breast:	n/a	n/a
49	MYC	chr14:67268467-67268547	MCF-7	breast:	n/a	n/a
50	MYC	chr14:67280630-67280781	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:67292488-67292538	BJ	skin:	n/a
2	chr14:67292488-67292538	HCT-116	colon:	n/a
3	chr14:67292488-67292538	NH-A	brain:	n/a
4	chr14:67292488-67292538	HUVEC	blood vessel:	n/a
5	chr14:67292488-67292538	H1-hESC	embryonic stem cell:	embryo
6	chr14:67292488-67292538	AoSMC	blood vessel:	n/a
7	chr14:67292488-67292538	NT2-D1	testis:	n/a
8	chr14:67292488-67292538	IMR90	lung:	fetal
9	chr14:67292488-67292538	SK-N-SH	brain:	n/a
10	chr14:67292488-67292538	BE2_C	brain:	n/a
11	chr14:67292488-67292538	GM06990	blood:	n/a
12	chr14:67292488-67292538	SK-N-SH_RA	brain:	n/a
13	chr14:67292488-67292538	SKMC	muscle:	n/a
14	chr14:67292488-67292538	RPTEC	kidney:	n/a
15	chr14:67292488-67292538	SAEC	small airway:	n/a
16	chr14:67292488-67292538	AG04449	skin:	fetal
17	chr14:67292488-67292538	NB4	blood:	n/a
18	chr14:67292488-67292538	HRPEpiC	eye:	n/a
19	chr14:67292488-67292538	Hela-S3	cervix:	n/a
20	chr14:67292488-67292538	U87	brain:	n/a
21	chr14:67292488-67292538	HCPEpiC	choroid plexus:	n/a
22	chr14:67292488-67292538	AG10803	skin:	n/a
23	chr14:67292488-67292538	HEK293	kidney:	embryo
24	chr14:67292488-67292538	AG09319	gingival:	n/a
25	chr14:67292488-67292538	SK-N-MC	brain:	n/a
26	chr14:67292488-67292538	Hepatocyte	liver:	n/a
27	chr14:67292488-67292538	HMEC	breast:	n/a
28	chr14:67292488-67292538	CMK	blood:	n/a
29	chr14:67292488-67292538	MCF-7	breast:	n/a
30	chr14:67292488-67292538	HepG2	liver:	n/a
31	chr14:67292488-67292538	NHBE	bronchial:	n/a
32	chr14:67292488-67292538	AG04450	lung:	fetal
33	chr14:67292488-67292538	HCM	heart:	n/a
34	chr14:67292488-67292538	GM12891	blood:	n/a
35	chr14:67292488-67292538	PANC-1	pancreas:	n/a
36	chr14:67292488-67292538	PrEC	prostate:	n/a
37	chr14:67292488-67292538	HL-60	blood:	n/a
38	chr14:67292488-67292538	HPAEpiC	pulmonary alveolar:	n/a
39	chr14:67292488-67292538	HCF	heart:	n/a
40	chr14:67292488-67292538	GM12892	blood:	n/a
41	chr14:67292488-67292538	LNCaP	prostate:	n/a
42	chr14:67292488-67292538	HNPCEpiC	eye:	n/a
43	chr14:67292488-67292538	A549	lung:	n/a
44	chr14:67292488-67292538	PFSK-1	brain:	n/a
45	chr14:67292488-67292538	HEEpiC	esophagus:	n/a
46	chr14:67292488-67292538	NHDF-neo	bronchial:	n/a
47	chr14:67292488-67292538	HRE	kidney:	n/a
48	chr14:67292488-67292538	HRCEpiC	kidney:	n/a
49	chr14:67292488-67292538	Caco-2	colon:	n/a
50	chr14:67292488-67292538	ovcar-3	ovarian:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:67297492..67297992-chr6:10786994..10787529,2	MCF-7	breast:
2	chr14:67292902..67294544-chr14:67295956..67298374,2	MCF-7	breast:
3	chr14:67292902..67294544-chr14:67295956..67298374,2	MCF-7	breast:
4	chr14:67273370..67275073-chr14:67291638..67294473,2	K562	blood:
5	chr14:67273370..67275073-chr14:67291638..67294473,2	K562	blood:
6	chr14:67290864..67292814-chr14:67296432..67298009,2	MCF-7	breast:

Variant related genes	Relation type
GPHN	TF binding region
GPHN	CpG island
ENSG00000171723	chromatin interactions

Extended variants
information (count: 1717 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:1717 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10149760	chr14:67261821-67261822	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs531969909	chr14:67261828-67261829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs140690135	chr14:67261983-67261984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs150490285	chr14:67261994-67261995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs183696568	chr14:67262023-67262024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs116614618	chr14:67262097-67262098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs543623412	chr14:67262262-67262263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs112439594	chr14:67262282-67262283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs561944955	chr14:67262323-67262324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs138339985	chr14:67262325-67262326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs548389339	chr14:67262355-67262356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs144059499	chr14:67262360-67262361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs188678406	chr14:67262386-67262387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs541751594	chr14:67262432-67262433	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs191426041	chr14:67262477-67262478	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs551411806	chr14:67262489-67262490	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs569807992	chr14:67262513-67262514	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs564439802	chr14:67262515-67262516	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs112080965	chr14:67262520-67262521	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs80008165	chr14:67262523-67262524	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs534973544	chr14:67262538-67262539	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs187175527	chr14:67262563-67262564	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs572016345	chr14:67262569-67262570	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs566713605	chr14:67262578-67262579	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs534077727	chr14:67262644-67262645	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs191537906	chr14:67262675-67262676	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs183727470	chr14:67262679-67262680	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs72728652	chr14:67262763-67262764	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs570863036	chr14:67262852-67262853	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs147301998	chr14:67262939-67262940	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs555235600	chr14:67263022-67263023	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs8008606	chr14:67263024-67263025	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs540923540	chr14:67263028-67263029	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs537818102	chr14:67263038-67263039	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs139197972	chr14:67263142-67263143	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs533402725	chr14:67263157-67263158	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs75622716	chr14:67263159-67263160	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs544986231	chr14:67263162-67263163	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs8008773	chr14:67263163-67263164	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs114661770	chr14:67263202-67263203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs186662683	chr14:67263221-67263222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs561277659	chr14:67263329-67263330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs192590156	chr14:67263445-67263446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs535591070	chr14:67263452-67263453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs9671368	chr14:67263455-67263456	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs143160010	chr14:67263460-67263461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs116212547	chr14:67263552-67263553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs551365297	chr14:67263556-67263557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs144728937	chr14:67263566-67263567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs536705246	chr14:67263579-67263580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian cancer	21720365	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Acute myeloid leukemia	21251322	CNVD
cataract	16735990	CNVD
Neuroblastoma	20406844	CNVD
Autism	22495309	CNVD
Breast cancer	21611746	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:265 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:67250800-67266400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr14:67255600-67280000	Weak transcription	Gastric	stomach
3	chr14:67256600-67262400	Weak transcription	Liver	Liver
4	chr14:67256600-67272600	Weak transcription	Ovary	ovary
5	chr14:67257600-67282000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr14:67259800-67263800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr14:67261000-67280000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr14:67261200-67268400	Weak transcription	Pancreas	Pancrea
9	chr14:67262400-67263200	Strong transcription	Liver	Liver
10	chr14:67263200-67272400	Weak transcription	Liver	Liver
11	chr14:67267200-67280000	Weak transcription	Stomach Smooth Muscle	stomach
12	chr14:67267400-67280000	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr14:67268000-67268200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr14:67268200-67268400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
15	chr14:67268200-67270200	ZNF genes & repeats	Fetal Intestine Small	intestine
16	chr14:67268200-67272200	Weak transcription	Duodenum Smooth Muscle	Duodenum
17	chr14:67268400-67268600	ZNF genes & repeats	Aorta	Aorta
18	chr14:67268400-67268600	Enhancers	Right Ventricle	heart
19	chr14:67268400-67268800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr14:67268400-67268800	ZNF genes & repeats	Pancreas	Pancrea
21	chr14:67268400-67269000	ZNF genes & repeats	Esophagus	oesophagus
22	chr14:67268400-67269200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr14:67268400-67271600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr14:67268600-67268800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr14:67268600-67280000	Weak transcription	Aorta	Aorta
26	chr14:67268600-67280000	Weak transcription	Right Ventricle	heart
27	chr14:67268800-67269000	ZNF genes & repeats	Fetal Stomach	stomach
28	chr14:67268800-67280000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr14:67268800-67280000	Weak transcription	Pancreas	Pancrea
30	chr14:67269000-67269400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr14:67269000-67272400	Weak transcription	Fetal Stomach	stomach
32	chr14:67269400-67280000	Weak transcription	Rectal Mucosa Donor 31	rectum
33	chr14:67269600-67269800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr14:67269600-67270000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr14:67269800-67270000	Enhancers	HepG2	liver
36	chr14:67269800-67271200	Enhancers	Primary hematopoietic stem cells short term culture	blood
37	chr14:67269800-67272400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr14:67270000-67274800	Weak transcription	HepG2	liver
39	chr14:67270000-67280000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr14:67270200-67271800	Weak transcription	Fetal Intestine Small	intestine
41	chr14:67270800-67271400	Enhancers	HUVEC	blood vessel
42	chr14:67270800-67272600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr14:67271600-67272200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
44	chr14:67271800-67272800	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr14:67271800-67273200	ZNF genes & repeats	Fetal Intestine Small	intestine
46	chr14:67271800-67280200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr14:67272200-67273400	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
48	chr14:67272400-67273000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr14:67272400-67273000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr14:67272400-67273000	ZNF genes & repeats	Liver	Liver

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