Variant report

Variant	nsv520814
Chromosome Location	chr14:20305431-20466824
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	ARID3A	chr14:20387153-20387455	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:20346227-20346537	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:20346241-20346527	K562	blood:	n/a	n/a
4	ATF1	chr14:20374096-20374405	K562	blood:	n/a	n/a
5	ATF1	chr14:20388271-20388560	K562	blood:	n/a	n/a
6	ATF1	chr14:20319622-20319703	K562	blood:	n/a	n/a
7	ATF1	chr14:20325048-20325100	K562	blood:	n/a	n/a
8	BACH1	chr14:20348120-20348235	K562	blood:	n/a	n/a
9	CBX3	chr14:20450329-20450560	K562	blood:	n/a	n/a
10	CEBPB	chr14:20370579-20370921	A549	lung:	n/a	chr14:20370744-20370755 chr14:20370732-20370743
11	CEBPB	chr14:20370643-20370895	Hela-S3	cervix:	n/a	chr14:20370744-20370755 chr14:20370732-20370743
12	CEBPB	chr14:20388060-20388537	A549	lung:	n/a	chr14:20388129-20388140
13	CEBPB	chr14:20370568-20370914	HepG2	liver:	n/a	chr14:20370744-20370755 chr14:20370732-20370743
14	CEBPB	chr14:20370645-20370888	K562	blood:	n/a	chr14:20370744-20370755 chr14:20370732-20370743
15	CEBPB	chr14:20439841-20439948	K562	blood:	n/a	chr14:20439867-20439880 chr14:20439867-20439878 chr14:20439867-20439880 chr14:20439868-20439879
16	CEBPB	chr14:20387030-20387353	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr14:20365988-20366164	HepG2	liver:	n/a	n/a
18	CEBPB	chr14:20439856-20439879	HepG2	liver:	n/a	chr14:20439867-20439878 chr14:20439868-20439879
19	CEBPB	chr14:20347421-20347704	K562	blood:	n/a	n/a
20	CEBPB	chr14:20386989-20387500	A549	lung:	n/a	n/a
21	CEBPB	chr14:20353081-20353403	A549	lung:	n/a	n/a
22	CEBPB	chr14:20386850-20387355	A549	lung:	n/a	n/a
23	CEBPB	chr14:20386291-20386625	HepG2	liver:	n/a	n/a
24	CEBPB	chr14:20439827-20439886	Hela-S3	cervix:	n/a	chr14:20439867-20439880 chr14:20439867-20439878 chr14:20439867-20439880 chr14:20439868-20439879
25	CEBPB	chr14:20439826-20440010	IMR90	lung:	n/a	chr14:20439990-20440001 chr14:20439867-20439880 chr14:20439867-20439878 chr14:20439867-20439880 chr14:20439868-20439879
26	CEBPB	chr14:20420582-20420802	HepG2	liver:	n/a	chr14:20420660-20420671
27	CEBPB	chr14:20388043-20388243	HepG2	liver:	n/a	chr14:20388129-20388140
28	CEBPB	chr14:20390412-20390477	HepG2	liver:	n/a	n/a
29	CEBPB	chr14:20346421-20346658	HepG2	liver:	n/a	chr14:20346574-20346585
30	CEBPB	chr14:20321015-20321026	K562	blood:	n/a	n/a
31	CEBPB	chr14:20353121-20353345	HepG2	liver:	n/a	n/a
32	CEBPB	chr14:20337012-20337281	K562	blood:	n/a	n/a
33	CEBPB	chr14:20420501-20420787	A549	lung:	n/a	chr14:20420660-20420671
34	CEBPB	chr14:20387024-20387360	HepG2	liver:	n/a	n/a
35	CEBPB	chr14:20386146-20386742	MCF-7	breast:	n/a	n/a
36	CEBPB	chr14:20374900-20375169	HepG2	liver:	n/a	chr14:20375036-20375045 chr14:20375036-20375047 chr14:20375036-20375045 chr14:20375034-20375045 chr14:20375036-20375045 chr14:20375034-20375047 chr14:20375036-20375047 chr14:20375036-20375045 chr14:20375034-20375047
37	CEBPB	chr14:20374855-20375196	IMR90	lung:	n/a	chr14:20375036-20375045 chr14:20375036-20375047 chr14:20375036-20375045 chr14:20375034-20375045 chr14:20375036-20375045 chr14:20375034-20375047 chr14:20375036-20375047 chr14:20375036-20375045 chr14:20375034-20375047
38	CEBPB	chr14:20374862-20375189	A549	lung:	n/a	chr14:20375036-20375045 chr14:20375036-20375047 chr14:20375036-20375045 chr14:20375034-20375045 chr14:20375036-20375045 chr14:20375034-20375047 chr14:20375036-20375047 chr14:20375036-20375045 chr14:20375034-20375047
39	CEBPB	chr14:20370608-20370903	IMR90	lung:	n/a	chr14:20370744-20370755 chr14:20370732-20370743
40	CEBPB	chr14:20387999-20388479	K562	blood:	n/a	chr14:20388129-20388140
41	CEBPB	chr14:20374865-20375205	K562	blood:	n/a	chr14:20375036-20375045 chr14:20375036-20375047 chr14:20375036-20375045 chr14:20375034-20375045 chr14:20375036-20375045 chr14:20375034-20375047 chr14:20375036-20375047 chr14:20375036-20375045 chr14:20375034-20375047
42	CEBPB	chr14:20434386-20434443	K562	blood:	n/a	n/a
43	CEBPB	chr14:20353091-20353443	IMR90	lung:	n/a	n/a
44	CEBPB	chr14:20386088-20387344	MCF-7	breast:	n/a	n/a
45	CEBPB	chr14:20413462-20413846	A549	lung:	n/a	n/a
46	CEBPB	chr14:20394073-20394339	HepG2	liver:	n/a	chr14:20394191-20394202
47	CEBPB	chr14:20434694-20434707	K562	blood:	n/a	n/a
48	CEBPB	chr14:20415039-20415202	HepG2	liver:	n/a	chr14:20415154-20415165
49	CEBPB	chr14:20439816-20439966	A549	lung:	n/a	chr14:20439867-20439880 chr14:20439867-20439878 chr14:20439867-20439880 chr14:20439868-20439879
50	CTCF	chr14:20386320-20386470	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:20344394-20344444	HEK293	kidney:	embryo
2	chr14:20389177-20389227	HRPEpiC	eye:	n/a
3	chr14:20344920-20344970	SK-N-MC	brain:	n/a
4	chr14:20404281-20404331	HRE	kidney:	n/a
5	chr14:20444164-20444214	PFSK-1	brain:	n/a
6	chr14:20403239-20403289	CMK	blood:	n/a
7	chr14:20387292-20387342	HEEpiC	esophagus:	n/a
8	chr14:20403239-20403289	SK-N-MC	brain:	n/a
9	chr14:20403845-20403895	HEK293	kidney:	embryo
10	chr14:20387292-20387342	AG09309	skin:	n/a
11	chr14:20389177-20389227	MCF-7	breast:	n/a
12	chr14:20344083-20344133	GM19239	blood:	n/a
13	chr14:20389177-20389227	BJ	skin:	n/a
14	chr14:20344394-20344444	RPTEC	kidney:	n/a
15	chr14:20344920-20344970	PANC-1	pancreas:	n/a
16	chr14:20444164-20444214	SKMC	muscle:	n/a
17	chr14:20344083-20344133	AG04449	skin:	fetal
18	chr14:20403845-20403895	HRE	kidney:	n/a
19	chr14:20344394-20344444	SAEC	small airway:	n/a
20	chr14:20403845-20403895	SAEC	small airway:	n/a
21	chr14:20404281-20404331	ovcar-3	ovarian:	n/a
22	chr14:20389177-20389227	Hela-S3	cervix:	n/a
23	chr14:20403845-20403895	GM12891	blood:	n/a
24	chr14:20404281-20404331	ProgFib	skin:	n/a
25	chr14:20404281-20404331	PrEC	prostate:	n/a
26	chr14:20403239-20403289	SK-N-SH	brain:	n/a
27	chr14:20387292-20387342	HCT-116	colon:	n/a
28	chr14:20444164-20444214	Jurkat	blood:	n/a
29	chr14:20389177-20389227	HRE	kidney:	n/a
30	chr14:20403845-20403895	RPTEC	kidney:	n/a
31	chr14:20344394-20344444	ProgFib	skin:	n/a
32	chr14:20404281-20404331	RPTEC	kidney:	n/a
33	chr14:20403845-20403895	GM12878	blood:	n/a
34	chr14:20344920-20344970	SK-N-SH_RA	brain:	n/a
35	chr14:20403239-20403289	HEEpiC	esophagus:	n/a
36	chr14:20403239-20403289	LNCaP	prostate:	n/a
37	chr14:20344083-20344133	NHDF-neo	bronchial:	n/a
38	chr14:20344083-20344133	NH-A	brain:	n/a
39	chr14:20389177-20389227	AG09319	gingival:	n/a
40	chr14:20389177-20389227	AG10803	skin:	n/a
41	chr14:20344920-20344970	RPTEC	kidney:	n/a
42	chr14:20444164-20444214	IMR90	lung:	fetal
43	chr14:20403845-20403895	MCF-7	breast:	n/a
44	chr14:20344920-20344970	ProgFib	skin:	n/a
45	chr14:20344083-20344133	AG09319	gingival:	n/a
46	chr14:20444164-20444214	HCM	heart:	n/a
47	chr14:20444164-20444214	HCPEpiC	choroid plexus:	n/a
48	chr14:20387292-20387342	HUVEC	blood vessel:	n/a
49	chr14:20389177-20389227	SKMC	muscle:	n/a
50	chr14:20444164-20444214	Hepatocyte	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:20421291..20423829-chr14:20424473..20427279,2	MCF-7	breast:
2	chr14:20453392..20455779-chr14:20560575..20562246,2	K562	blood:
3	chr14:20382435..20385861-chr14:20389212..20390807,3	K562	blood:
4	chr14:20330082..20332945-chr14:20336237..20338891,2	K562	blood:
5	chr14:20382435..20385861-chr14:20389212..20390807,3	K562	blood:
6	chr14:20378405..20379102-chr22:33621834..33622612,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR4K14-1	chr14:20376255-20376808	NONHSAT035546

Variant related genes	Relation type
ENSG00000259016	TF binding region
OR4K5	TF binding region
OR4K15	TF binding region
OR4Q2	TF binding region
OR4K4P	TF binding region
OR4K3	TF binding region
OR4K6P	TF binding region
OR4K16P	TF binding region
OR4K1	TF binding region
OR4K2	TF binding region
ENSG00000259016	CpG island
OR4K5	CpG island
OR4K15	CpG island
OR4Q2	CpG island
OR4K4P	CpG island
OR4K3	CpG island
OR4K6P	CpG island
OR4K16P	CpG island
OR4K1	CpG island
OR4K2	CpG island
ENSG00000258822	chromatin interactions
ENSG00000258641	chromatin interactions
ENSG00000176290	chromatin interactions

Extended variants
information (count: 3765 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:3765 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551068005	chr14:20306422-20306423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs569450647	chr14:20306471-20306472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs537144444	chr14:20306525-20306526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs548226972	chr14:20306539-20306540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs556516575	chr14:20306564-20306565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs188304387	chr14:20306568-20306569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs569651257	chr14:20306625-20306626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs537019189	chr14:20306631-20306632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs535797549	chr14:20306666-20306667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs554401343	chr14:20306680-20306681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs572480501	chr14:20306685-20306686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs58583292	chr14:20306696-20306697	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs558180776	chr14:20306726-20306727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs368972261	chr14:20306730-20306731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs370252616	chr14:20306761-20306762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs201752341	chr14:20306763-20306764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs372373541	chr14:20306764-20306765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs199761313	chr14:20306791-20306792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs200691865	chr14:20306792-20306793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs71108561	chr14:20306795-20306796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs2318529	chr14:20306796-20306797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs554388784	chr14:20306799-20306800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs76884003	chr14:20306800-20306801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs201442691	chr14:20306801-20306802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs2318528	chr14:20306806-20306807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs149887475	chr14:20306812-20306813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs2873716	chr14:20306814-20306815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs2873715	chr14:20306816-20306817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs146527221	chr14:20306823-20306824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs111229568	chr14:20306832-20306833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs71108562	chr14:20306836-20306837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs543881469	chr14:20306859-20306860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs180876985	chr14:20306885-20306886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs376176606	chr14:20306974-20306975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs529053831	chr14:20306983-20306984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs540968389	chr14:20307034-20307035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs559181207	chr14:20307070-20307071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs533047170	chr14:20307100-20307101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs370764084	chr14:20307108-20307109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs377040100	chr14:20307150-20307151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs551008523	chr14:20307171-20307172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs145053760	chr14:20307191-20307192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs551769950	chr14:20307246-20307247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs562921247	chr14:20307275-20307276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs541510341	chr14:20307297-20307298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs35964660	chr14:20307332-20307333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs61976686	chr14:20307337-20307338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs186517392	chr14:20307351-20307352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs138978768	chr14:20307419-20307420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs568564561	chr14:20307434-20307435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Cancer	20164920	CNVD
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
Cone-rod dystrophy	18421352	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	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
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	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
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Alzheimer''s disease	21482944	CNVD
Mental retardation	19951919	CNVD
Neuroblastoma	21899760	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Esophageal cancer	20955586	CNVD
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17440070	CNVD
Breast cancer	16272173	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
Breast cancer	21509527	CNVD
Autism	20531469	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:101 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:20306400-20308200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr14:20308400-20308800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr14:20308800-20312400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr14:20312400-20313000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr14:20324200-20328800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
6	chr14:20329200-20330800	Enhancers	Pancreatic Islets	Pancreatic Islet
7	chr14:20330600-20331400	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
8	chr14:20341000-20341600	Active TSS	ES-I3 Cell Line	embryonic stem cell
9	chr14:20341000-20341600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
10	chr14:20341200-20341400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr14:20341200-20341400	Active TSS	Adipose Nuclei	Adipose
12	chr14:20341200-20341400	Bivalent/Poised TSS	Brain Angular Gyrus	brain
13	chr14:20341200-20341400	Flanking Active TSS	A549	lung
14	chr14:20341200-20341600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr14:20341200-20341600	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
16	chr14:20341200-20341600	Active TSS	K562	blood
17	chr14:20341400-20341600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr14:20341400-20341600	Flanking Active TSS	Adipose Nuclei	Adipose
19	chr14:20341400-20341600	Bivalent Enhancer	Brain Angular Gyrus	brain
20	chr14:20341400-20341800	Active TSS	A549	lung
21	chr14:20341600-20341800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr14:20341600-20341800	Enhancers	Adipose Nuclei	Adipose
23	chr14:20341600-20341800	Bivalent Enhancer	Stomach Smooth Muscle	stomach
24	chr14:20342800-20343400	Enhancers	HepG2	liver
25	chr14:20343200-20352400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
26	chr14:20350200-20350400	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
27	chr14:20351200-20351600	ZNF genes & repeats	Fetal Brain Male	brain
28	chr14:20351200-20352200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
29	chr14:20351200-20354200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr14:20355400-20356200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
31	chr14:20355800-20358400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
32	chr14:20359000-20366000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr14:20360400-20363800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
34	chr14:20360600-20364000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
35	chr14:20361800-20364200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr14:20362000-20363200	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
37	chr14:20362400-20364800	ZNF genes & repeats	Adipose Nuclei	Adipose
38	chr14:20368800-20370800	Enhancers	Adipose Nuclei	Adipose
39	chr14:20369000-20379600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
40	chr14:20370200-20372000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
41	chr14:20373800-20374600	ZNF genes & repeats	Fetal Brain Male	brain
42	chr14:20374200-20374600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr14:20378200-20379400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
44	chr14:20383200-20385000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
45	chr14:20386400-20386800	Enhancers	Pancreatic Islets	Pancreatic Islet
46	chr14:20386800-20389000	Weak transcription	Pancreatic Islets	Pancreatic Islet
47	chr14:20388200-20391000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr14:20389000-20389200	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
49	chr14:20389000-20389600	Active TSS	Brain Substantia Nigra	brain
50	chr14:20389200-20390000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell

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