Variant report

Variant	esv1825293
Chromosome Location	chr14:70020620-70039587
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	chr14:70036661-70036871	HepG2	liver:	n/a	n/a
2	CEBPB	chr14:70036736-70036894	HepG2	liver:	n/a	n/a
3	CHD2	chr14:70039330-70039421	H1-hESC	embryonic stem cell:	n/a	n/a
4	CHD2	chr14:70038693-70038959	H1-hESC	embryonic stem cell:	n/a	n/a
5	CTCF	chr14:70036800-70036950	HRE	kidney:	n/a	chr14:70036896-70036914
6	CTCF	chr14:70039069-70039170	LNCaP	prostate:	n/a	n/a
7	CTCF	chr14:70039246-70039254	LNCaP	prostate:	n/a	n/a
8	CTCF	chr14:70039180-70039330	AG04449	skin:	n/a	chr14:70039271-70039284 chr14:70039283-70039296
9	CTCF	chr14:70022166-70022239	Hela-S3	cervix:	n/a	n/a
10	CTCF	chr14:70024140-70024290	AG09309	skin:	n/a	n/a
11	CTCF	chr14:70023440-70023590	BE2_C	brain:	n/a	n/a
12	CTCF	chr14:70039177-70039191	LNCaP	prostate:	n/a	n/a
13	CTCF	chr14:70022060-70022210	MCF-7	breast:	n/a	n/a
14	CTCF	chr14:70036882-70036905	Hela-S3	cervix:	n/a	n/a
15	CTCF	chr14:70038520-70038670	NHEK	skin:	n/a	chr14:70038578-70038591
16	CTCF	chr14:70039238-70039245	LNCaP	prostate:	n/a	n/a
17	CTCF	chr14:70036720-70036870	MCF-7	breast:	n/a	n/a
18	CTCF	chr14:70021340-70021490	SK-N-SH_RA	brain:	n/a	n/a
19	E2F4	chr14:70037758-70037817	MCF10A-Er-Src	breast:	n/a	n/a
20	E2F6	chr14:70038047-70039768	H1-hESC	embryonic stem cell:	n/a	chr14:70039052-70039062 chr14:70039095-70039104 chr14:70039088-70039098 chr14:70038869-70038880 chr14:70039085-70039095
21	E2F6	chr14:70038912-70039341	K562	blood:	n/a	chr14:70039052-70039062 chr14:70039095-70039104 chr14:70039088-70039098 chr14:70039085-70039095
22	E2F6	chr14:70037838-70041874	H1-hESC	embryonic stem cell:	n/a	chr14:70039917-70039926 chr14:70040055-70040065 chr14:70039052-70039062 chr14:70039095-70039104 chr14:70039088-70039098 chr14:70039907-70039917 chr14:70038869-70038880 chr14:70041273-70041288 chr14:70041340-70041349 chr14:70039085-70039095
23	E2F6	chr14:70038151-70039756	A549	lung:	n/a	chr14:70039052-70039062 chr14:70039095-70039104 chr14:70039088-70039098 chr14:70038869-70038880 chr14:70039085-70039095
24	E2F6	chr14:70038338-70039010	A549	lung:	n/a	chr14:70038869-70038880
25	EP300	chr14:70038439-70039405	ECC-1	luminal epithelium:	n/a	chr14:70039010-70039026 chr14:70039001-70039017 chr14:70039088-70039097 chr14:70038671-70038687
26	FOS	chr14:70038872-70039291	HUVEC	blood vessel:	n/a	n/a
27	GABPA	chr14:70038497-70039215	H1-hESC	embryonic stem cell:	n/a	chr14:70039008-70039017
28	GABPA	chr14:70039041-70039653	H1-hESC	embryonic stem cell:	n/a	n/a
29	GABPA	chr14:70038534-70039003	H1-hESC	embryonic stem cell:	n/a	n/a
30	GTF2F1	chr14:70038370-70039388	H1-hESC	embryonic stem cell:	n/a	n/a
31	HA-E2F1	chr14:70038587-70039423	MCF-7	breast:	n/a	chr14:70039052-70039062 chr14:70039095-70039104 chr14:70039088-70039098 chr14:70038869-70038880 chr14:70039085-70039095
32	HDAC2	chr14:70038857-70039186	HepG2	liver:	n/a	n/a
33	HEY1	chr14:70020420-70020659	K562	blood:	n/a	n/a
34	HNF4A	chr14:70036597-70036855	HepG2	liver:	n/a	n/a
35	IRF1	chr14:70020712-70020718	K562	blood:	n/a	n/a
36	KAP1	chr14:70038694-70039403	HEK293	kidney:	n/a	n/a
37	MAFF	chr14:70027668-70027833	HepG2	liver:	n/a	n/a
38	MAFF	chr14:70027716-70027768	K562	blood:	n/a	n/a
39	MAFK	chr14:70027645-70027815	HepG2	liver:	n/a	n/a
40	MAFK	chr14:70027620-70027858	IMR90	lung:	n/a	n/a
41	MAFK	chr14:70027587-70027911	HepG2	liver:	n/a	n/a
42	MAX	chr14:70038631-70039065	A549	lung:	n/a	n/a
43	MAX	chr14:70038147-70039969	A549	lung:	n/a	chr14:70038494-70038503 chr14:70039385-70039392 chr14:70039384-70039393 chr14:70039728-70039737 chr14:70038304-70038313 chr14:70038305-70038312
44	MAX	chr14:70038011-70039766	ECC-1	luminal epithelium:	n/a	chr14:70038494-70038503 chr14:70039385-70039392 chr14:70039384-70039393 chr14:70039728-70039737 chr14:70038304-70038313 chr14:70038305-70038312
45	MAX	chr14:70038664-70039422	HepG2	liver:	n/a	chr14:70039385-70039392 chr14:70039384-70039393
46	MAX	chr14:70038551-70039533	MCF-7	breast:	n/a	chr14:70039385-70039392 chr14:70039384-70039393
47	MAX	chr14:70039164-70039569	HUVEC	blood vessel:	n/a	chr14:70039385-70039392 chr14:70039384-70039393
48	MAX	chr14:70038645-70039534	MCF-7	breast:	n/a	chr14:70039385-70039392 chr14:70039384-70039393
49	MAX	chr14:70038221-70039565	A549	lung:	n/a	chr14:70038494-70038503 chr14:70039385-70039392 chr14:70039384-70039393 chr14:70038304-70038313 chr14:70038305-70038312
50	MAX	chr14:70039009-70039308	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:70037728-70037778	GM12878	blood:	n/a
2	chr14:70039262-70039312	AoSMC	blood vessel:	n/a
3	chr14:70037728-70037778	GM12878	blood:	n/a
4	chr14:70039262-70039312	AoSMC	blood vessel:	n/a
5	chr14:70038925-70038975	NB4	blood:	n/a
6	chr14:70037728-70037778	SK-N-MC	brain:	n/a
7	chr14:70037728-70037778	HCT-116	colon:	n/a
8	chr14:70038949-70038999	SK-N-MC	brain:	n/a
9	chr14:70038949-70038999	NB4	blood:	n/a
10	chr14:70037728-70037778	HMEC	breast:	n/a
11	chr14:70034401-70034451	HRCEpiC	kidney:	n/a
12	chr14:70034401-70034451	NHBE	bronchial:	n/a
13	chr14:70039262-70039312	K562	blood:	n/a
14	chr14:70037973-70038023	HCT-116	colon:	n/a
15	chr14:70038717-70038767	IMR90	lung:	fetal
16	chr14:70038925-70038975	CMK	blood:	n/a
17	chr14:70034401-70034451	SK-N-MC	brain:	n/a
18	chr14:70039262-70039312	T-47D	breast:	n/a
19	chr14:70037728-70037778	SKMC	muscle:	n/a
20	chr14:70038925-70038975	HRE	kidney:	n/a
21	chr14:70038949-70038999	PANC-1	pancreas:	n/a
22	chr14:70039262-70039312	AG04450	lung:	fetal
23	chr14:70038236-70038286	AG04450	lung:	fetal
24	chr14:70038717-70038767	AoSMC	blood vessel:	n/a
25	chr14:70038073-70038123	ECC-1	luminal epithelium:	n/a
26	chr14:70038884-70038934	HAEpiC	amniotic membrane:	n/a
27	chr14:70038884-70038934	HIPEpiC	eye:	n/a
28	chr14:70038949-70038999	HIPEpiC	eye:	n/a
29	chr14:70037973-70038023	AoSMC	blood vessel:	n/a
30	chr14:70034401-70034451	GM12892	blood:	n/a
31	chr14:70038073-70038123	T-47D	breast:	n/a
32	chr14:70038505-70038555	U87	brain:	n/a
33	chr14:70038717-70038767	Jurkat	blood:	n/a
34	chr14:70038236-70038286	ovcar-3	ovarian:	n/a
35	chr14:70038925-70038975	ECC-1	luminal epithelium:	n/a
36	chr14:70038884-70038934	SK-N-SH_RA	brain:	n/a
37	chr14:70037973-70038023	MCF10A-Er-Src	breast:	n/a
38	chr14:70034401-70034451	HMEC	breast:	n/a
39	chr14:70038717-70038767	SK-N-SH	brain:	n/a
40	chr14:70038925-70038975	HL-60	blood:	n/a
41	chr14:70038505-70038555	Jurkat	blood:	n/a
42	chr14:70034401-70034451	RPTEC	kidney:	n/a
43	chr14:70038236-70038286	MCF10A-Er-Src	breast:	n/a
44	chr14:70039262-70039312	AG09309	skin:	n/a
45	chr14:70038717-70038767	HRCEpiC	kidney:	n/a
46	chr14:70037728-70037778	NHDF-neo	bronchial:	n/a
47	chr14:70038236-70038286	GM06990	blood:	n/a
48	chr14:70038505-70038555	GM06990	blood:	n/a
49	chr14:70038717-70038767	PANC-1	pancreas:	n/a
50	chr14:70038717-70038767	AG09319	gingival:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:70026545..70029008-chr14:70036347..70037973,2	K562	blood:
2	chr14:70031632..70033934-chr14:70036224..70037978,2	MCF-7	breast:
3	chr14:70017252..70019408-chr14:70020667..70022465,2	MCF-7	breast:
4	chr14:70037278..70041103-chr14:70232570..70234461,4	MCF-7	breast:
5	chr14:70030422..70032723-chr14:70038343..70040590,3	MCF-7	breast:
6	chr14:69949714..69952374-chr14:70039182..70041131,3	MCF-7	breast:
7	chr14:70030912..70032771-chr14:70037845..70040313,2	K562	blood:
8	chr14:70019966..70021611-chr14:70026583..70029344,2	K562	blood:
9	chr14:70036912..70038706-chr14:70040330..70041890,2	MCF-7	breast:
10	chr14:70013357..70015397-chr14:70020516..70022458,2	K562	blood:
11	chr14:70001853..70002635-chr14:70034399..70035068,2	MCF-7	breast:
12	chr14:70031632..70033934-chr14:70036224..70037978,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PLEKHD1-2	chr14:70031849-70032228	NONHSAT037531
2	lnc-C14orf162-2	chr14:70027736-70028187	NONHSAT037530
3	lnc-C14orf162-1	chr14:70036532-70037918	NONHSAT037533
4	lnc-PLEKHD1-2	chr14:70033206-70033228	NONHSAT037531

Variant related genes	Relation type
ENSG00000244237	TF binding region
CCDC177	TF binding region
ENSG00000244237	CpG island
CCDC177	CpG island
ENSG00000267909	chromatin interactions
ENSG00000255994	chromatin interactions
ENSG00000100650	chromatin interactions
ENSG00000175985	chromatin interactions
ENSG00000244237	chromatin interactions

Extended variants
information (count: 696 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:696 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547619795	chr14:70020635-70020636	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs562684304	chr14:70020660-70020661	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs566022215	chr14:70020661-70020662	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs371486553	chr14:70020669-70020670	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs548966491	chr14:70020690-70020691	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs199683255	chr14:70020691-70020692	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs186078126	chr14:70020754-70020755	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs145138950	chr14:70020771-70020772	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs114609377	chr14:70020781-70020782	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs564550308	chr14:70020785-70020786	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs546611883	chr14:70020794-70020795	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs144665600	chr14:70020824-70020825	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs146709628	chr14:70020856-70020857	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs550683269	chr14:70020943-70020944	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs183312632	chr14:70020944-70020945	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs34519327	chr14:70020955-70020956	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs568979776	chr14:70020960-70020961	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs34124235	chr14:70020987-70020988	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs373405429	chr14:70020988-70020989	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs74061850	chr14:70020989-70020990	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs71446394	chr14:70020997-70020998	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs570036373	chr14:70021001-70021002	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs548226034	chr14:70021036-70021037	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs547029465	chr14:70021084-70021085	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs563110391	chr14:70021110-70021111	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs192374759	chr14:70021141-70021142	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs372624435	chr14:70021149-70021150	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs182441162	chr14:70021178-70021179	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs187914860	chr14:70021187-70021188	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs192543305	chr14:70021189-70021190	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs538059746	chr14:70021201-70021202	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs117500218	chr14:70021210-70021211	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs182708491	chr14:70021241-70021242	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs200616825	chr14:70021255-70021256	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs369489843	chr14:70021290-70021291	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs397809766	chr14:70021291-70021292	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs374668502	chr14:70021293-70021294	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs187341057	chr14:70021294-70021295	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs541787527	chr14:70021336-70021337	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs560521951	chr14:70021343-70021344	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs11851273	chr14:70021348-70021349	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs540516262	chr14:70021367-70021368	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs565072014	chr14:70021417-70021418	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs532291181	chr14:70021448-70021449	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs192240562	chr14:70021465-70021466	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs562538662	chr14:70021483-70021484	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs9630396	chr14:70021562-70021563	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs553558208	chr14:70021591-70021592	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs143568648	chr14:70021611-70021612	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs566461207	chr14:70021680-70021681	Weak transcription Enhancers	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
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
cataract	16735990	CNVD
Neuroblastoma	20406844	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	20067559	CNVD

Chromatin state (count:333 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:70015000-70026200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr14:70015200-70026000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr14:70016600-70026000	Weak transcription	Fetal Brain Female	brain
4	chr14:70019200-70021400	Enhancers	Hela-S3	cervix
5	chr14:70020400-70025800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr14:70020600-70025800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr14:70021200-70021800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
8	chr14:70021400-70021800	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr14:70021400-70021800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr14:70021600-70021800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
11	chr14:70022600-70022800	Enhancers	Brain Germinal Matrix	brain
12	chr14:70022800-70026200	Weak transcription	Brain Germinal Matrix	brain
13	chr14:70025400-70029800	Enhancers	Cortex derived primary cultured neurospheres	brain
14	chr14:70025800-70026200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr14:70025800-70026200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr14:70025800-70028000	Enhancers	Fetal Brain Male	brain
17	chr14:70025800-70028200	Enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr14:70025800-70028400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr14:70026000-70026200	Enhancers	Fetal Brain Female	brain
20	chr14:70026000-70026600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
21	chr14:70026000-70026800	Bivalent Enhancer	Fetal Stomach	stomach
22	chr14:70026000-70027000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr14:70026000-70027000	Enhancers	Brain Angular Gyrus	brain
24	chr14:70026000-70027000	Enhancers	Brain Cingulate Gyrus	brain
25	chr14:70026000-70028200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr14:70026200-70026400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr14:70026200-70026400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr14:70026200-70026400	Bivalent Enhancer	Placenta	Placenta
29	chr14:70026200-70026600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr14:70026200-70026600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr14:70026200-70026600	Flanking Active TSS	Fetal Brain Female	brain
32	chr14:70026200-70026600	Bivalent Enhancer	Fetal Muscle Leg	muscle
33	chr14:70026200-70026600	Bivalent Enhancer	Fetal Thymus	thymus
34	chr14:70026200-70026800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr14:70026200-70026800	Enhancers	HMEC	breast
36	chr14:70026200-70027000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr14:70026200-70027000	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr14:70026200-70027000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr14:70026200-70027000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr14:70026200-70027000	Enhancers	Brain Substantia Nigra	brain
41	chr14:70026200-70027200	Enhancers	Brain Anterior Caudate	brain
42	chr14:70026200-70027200	Enhancers	Brain Hippocampus Middle	brain
43	chr14:70026200-70027200	Enhancers	Brain Inferior Temporal Lobe	brain
44	chr14:70026200-70027400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
45	chr14:70026200-70027800	Enhancers	Brain Germinal Matrix	brain
46	chr14:70026400-70026800	Bivalent Enhancer	NHEK	skin
47	chr14:70026400-70028600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr14:70026600-70026800	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr14:70026600-70028000	Enhancers	Fetal Brain Female	brain
50	chr14:70026800-70027000	Enhancers	HUES64 Cell Line	embryonic stem cell

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