Variant report

Variant	nsv565004
Chromosome Location	chr14:70035500-70041363
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	chr14:70041259-70041667	H1-hESC	embryonic stem cell:	n/a	n/a
5	CHD2	chr14:70038693-70038959	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTCF	chr14:70041271-70042031	HCT-116	colon:	n/a	chr14:70041613-70041626 chr14:70041612-70041628 chr14:70041613-70041626 chr14:70041611-70041629
7	CTCF	chr14:70040977-70042126	A549	lung:	n/a	chr14:70041613-70041626 chr14:70041141-70041154 chr14:70041612-70041628 chr14:70041613-70041626 chr14:70041611-70041629
8	CTCF	chr14:70041243-70041738	T-47D	breast:	n/a	chr14:70041613-70041626 chr14:70041612-70041628 chr14:70041613-70041626 chr14:70041611-70041629
9	CTCF	chr14:70041160-70041310	SAEC	small airway:	n/a	n/a
10	CTCF	chr14:70041200-70041350	AG04449	skin:	n/a	n/a
11	CTCF	chr14:70039180-70039330	AG04449	skin:	n/a	chr14:70039271-70039284 chr14:70039283-70039296
12	CTCF	chr14:70040900-70041050	HCM	heart:	n/a	n/a
13	CTCF	chr14:70041331-70041393	Lung_OC	lung:	n/a	n/a
14	CTCF	chr14:70036720-70036870	MCF-7	breast:	n/a	n/a
15	CTCF	chr14:70041262-70041885	HCT-116	colon:	n/a	chr14:70041613-70041626 chr14:70041612-70041628 chr14:70041613-70041626 chr14:70041611-70041629
16	CTCF	chr14:70036800-70036950	HRE	kidney:	n/a	chr14:70036896-70036914
17	CTCF	chr14:70041356-70041827	T-47D	breast:	n/a	chr14:70041613-70041626 chr14:70041612-70041628 chr14:70041613-70041626 chr14:70041611-70041629
18	CTCF	chr14:70039177-70039191	LNCaP	prostate:	n/a	n/a
19	CTCF	chr14:70041180-70041330	GM12874	blood:	n/a	n/a
20	CTCF	chr14:70036882-70036905	Hela-S3	cervix:	n/a	n/a
21	CTCF	chr14:70041160-70041310	HCM	heart:	n/a	n/a
22	CTCF	chr14:70041235-70041971	MCF-7	breast:	n/a	chr14:70041613-70041626 chr14:70041612-70041628 chr14:70041613-70041626 chr14:70041611-70041629
23	CTCF	chr14:70039246-70039254	LNCaP	prostate:	n/a	n/a
24	CTCF	chr14:70038520-70038670	NHEK	skin:	n/a	chr14:70038578-70038591
25	CTCF	chr14:70039069-70039170	LNCaP	prostate:	n/a	n/a
26	CTCF	chr14:70041070-70042069	SK-N-SH	brain:	n/a	chr14:70041613-70041626 chr14:70041141-70041154 chr14:70041612-70041628 chr14:70041613-70041626 chr14:70041611-70041629
27	CTCF	chr14:70039238-70039245	LNCaP	prostate:	n/a	n/a
28	CTCF	chr14:70041100-70041250	AG04450	lung:	n/a	chr14:70041141-70041154
29	CTCF	chr14:70041323-70041711	K562	blood:	n/a	chr14:70041613-70041626 chr14:70041612-70041628 chr14:70041613-70041626 chr14:70041611-70041629
30	E2F4	chr14:70037758-70037817	MCF10A-Er-Src	breast:	n/a	n/a
31	E2F6	chr14:70038912-70039341	K562	blood:	n/a	chr14:70039052-70039062 chr14:70039095-70039104 chr14:70039088-70039098 chr14:70039085-70039095
32	E2F6	chr14:70038338-70039010	A549	lung:	n/a	chr14:70038869-70038880
33	E2F6	chr14:70041152-70041792	H1-hESC	embryonic stem cell:	n/a	chr14:70041273-70041288 chr14:70041340-70041349
34	E2F6	chr14:70038151-70039756	A549	lung:	n/a	chr14:70039052-70039062 chr14:70039095-70039104 chr14:70039088-70039098 chr14:70038869-70038880 chr14:70039085-70039095
35	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
36	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
37	EP300	chr14:70038439-70039405	ECC-1	luminal epithelium:	n/a	chr14:70039010-70039026 chr14:70039001-70039017 chr14:70039088-70039097 chr14:70038671-70038687
38	FOS	chr14:70038872-70039291	HUVEC	blood vessel:	n/a	n/a
39	GABPA	chr14:70040363-70040890	H1-hESC	embryonic stem cell:	n/a	n/a
40	GABPA	chr14:70038497-70039215	H1-hESC	embryonic stem cell:	n/a	chr14:70039008-70039017
41	GABPA	chr14:70038534-70039003	H1-hESC	embryonic stem cell:	n/a	n/a
42	GABPA	chr14:70039041-70039653	H1-hESC	embryonic stem cell:	n/a	n/a
43	GABPA	chr14:70041085-70041683	H1-hESC	embryonic stem cell:	n/a	chr14:70041334-70041348
44	GTF2F1	chr14:70040637-70040762	H1-hESC	embryonic stem cell:	n/a	n/a
45	GTF2F1	chr14:70038370-70039388	H1-hESC	embryonic stem cell:	n/a	n/a
46	GTF2F1	chr14:70041293-70041684	H1-hESC	embryonic stem cell:	n/a	n/a
47	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
48	HDAC2	chr14:70038857-70039186	HepG2	liver:	n/a	n/a
49	HNF4A	chr14:70036597-70036855	HepG2	liver:	n/a	n/a
50	KAP1	chr14:70038694-70039403	HEK293	kidney:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:70041214-70041264	PrEC	prostate:	n/a
2	chr14:70041214-70041264	PrEC	prostate:	n/a
3	chr14:70041214-70041264	T-47D	breast:	n/a
4	chr14:70038925-70038975	HEEpiC	esophagus:	n/a
5	chr14:70041283-70041333	NB4	blood:	n/a
6	chr14:70039262-70039312	RPTEC	kidney:	n/a
7	chr14:70038925-70038975	MCF10A-Er-Src	breast:	n/a
8	chr14:70037728-70037778	ovcar-3	ovarian:	n/a
9	chr14:70041214-70041264	Jurkat	blood:	n/a
10	chr14:70041283-70041333	SKMC	muscle:	n/a
11	chr14:70038073-70038123	GM06990	blood:	n/a
12	chr14:70041214-70041264	HCF	heart:	n/a
13	chr14:70041283-70041333	A549	lung:	n/a
14	chr14:70038073-70038123	U87	brain:	n/a
15	chr14:70041283-70041333	PANC-1	pancreas:	n/a
16	chr14:70039915-70039965	AG09309	skin:	n/a
17	chr14:70037973-70038023	SK-N-SH	brain:	n/a
18	chr14:70041283-70041333	Hela-S3	cervix:	n/a
19	chr14:70038884-70038934	HCPEpiC	choroid plexus:	n/a
20	chr14:70038949-70038999	K562	blood:	n/a
21	chr14:70040899-70040949	H1-hESC	embryonic stem cell:	embryo
22	chr14:70039262-70039312	GM06990	blood:	n/a
23	chr14:70040899-70040949	HEEpiC	esophagus:	n/a
24	chr14:70038236-70038286	GM12891	blood:	n/a
25	chr14:70038925-70038975	U87	brain:	n/a
26	chr14:70039915-70039965	SK-N-SH	brain:	n/a
27	chr14:70037973-70038023	AG04449	skin:	fetal
28	chr14:70041214-70041264	Hepatocyte	liver:	n/a
29	chr14:70041283-70041333	ovcar-3	ovarian:	n/a
30	chr14:70038925-70038975	SK-N-SH	brain:	n/a
31	chr14:70040391-70040441	SK-N-SH_RA	brain:	n/a
32	chr14:70041283-70041333	PFSK-1	brain:	n/a
33	chr14:70037973-70038023	GM12892	blood:	n/a
34	chr14:70039915-70039965	AG10803	skin:	n/a
35	chr14:70038505-70038555	NHDF-neo	bronchial:	n/a
36	chr14:70038505-70038555	AG09319	gingival:	n/a
37	chr14:70039262-70039312	NT2-D1	testis:	n/a
38	chr14:70041214-70041264	GM06990	blood:	n/a
39	chr14:70037973-70038023	HEEpiC	esophagus:	n/a
40	chr14:70038236-70038286	NB4	blood:	n/a
41	chr14:70038884-70038934	BJ	skin:	n/a
42	chr14:70039915-70039965	HCM	heart:	n/a
43	chr14:70038717-70038767	HIPEpiC	eye:	n/a
44	chr14:70037728-70037778	NHDF-neo	bronchial:	n/a
45	chr14:70038505-70038555	GM12878	blood:	n/a
46	chr14:70040391-70040441	ProgFib	skin:	n/a
47	chr14:70040391-70040441	SK-N-MC	brain:	n/a
48	chr14:70037728-70037778	SK-N-SH	brain:	n/a
49	chr14:70038884-70038934	HRE	kidney:	n/a
50	chr14:70038236-70038286	T-47D	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:69949714..69952374-chr14:70039182..70041131,3	MCF-7	breast:
2	chr14:69970362..69971107-chr14:70041144..70041646,2	K562	blood:
3	chr14:69709466..69710008-chr14:70041288..70042008,2	MCF-7	breast:
4	chr14:70001682..70002652-chr14:70041139..70042080,9	MCF-7	breast:
5	chr14:69970369..69971161-chr14:70041166..70042114,4	MCF-7	breast:
6	chr14:70036912..70038706-chr14:70040330..70041890,2	MCF-7	breast:
7	chr14:70036912..70038706-chr14:70040330..70041890,2	MCF-7	breast:
8	chr14:70037278..70041103-chr14:70232570..70234461,4	MCF-7	breast:
9	chr14:70031632..70033934-chr14:70036224..70037978,2	MCF-7	breast:
10	chr14:70041091..70041642-chr14:70193316..70193928,2	MCF-7	breast:
11	chr14:70026545..70029008-chr14:70036347..70037973,2	K562	blood:
12	chr14:70001699..70002644-chr14:70040741..70042019,6	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C14orf162-1	chr14:70036532-70037918	NONHSAT037533

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

Extended variants
information (count: 193 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:193 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8008869	chr14:70035500-70035501	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs377551318	chr14:70035502-70035503	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs141585877	chr14:70035529-70035530	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs186767301	chr14:70035579-70035580	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs571215993	chr14:70035593-70035594	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs115151052	chr14:70035622-70035623	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs116309505	chr14:70035625-70035626	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs557285610	chr14:70035693-70035694	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs575659113	chr14:70035707-70035708	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs374552577	chr14:70035734-70035735	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs78150489	chr14:70035737-70035738	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs531939778	chr14:70035756-70035757	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs535641788	chr14:70035832-70035833	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs376332569	chr14:70035840-70035841	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs549958655	chr14:70035869-70035870	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs568560122	chr14:70035875-70035876	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs565484009	chr14:70035893-70035894	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs74606156	chr14:70035907-70035908	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs547795942	chr14:70035921-70035922	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs140302309	chr14:70035941-70035942	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs534075887	chr14:70035962-70035963	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs112868794	chr14:70035980-70035981	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs1957370	chr14:70036009-70036010	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs192788682	chr14:70036012-70036013	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs374801488	chr14:70036017-70036018	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs147389385	chr14:70036050-70036051	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs554504435	chr14:70036151-70036152	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs534300994	chr14:70036152-70036153	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs182899658	chr14:70036183-70036184	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs573011919	chr14:70036212-70036213	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs35371371	chr14:70036224-70036225	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs139663355	chr14:70036234-70036235	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs374692840	chr14:70036255-70036256	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs375126780	chr14:70036415-70036416	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs571751661	chr14:70036418-70036419	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs79720751	chr14:70036427-70036428	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs149938595	chr14:70036459-70036460	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs531781533	chr14:70036487-70036488	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs565038692	chr14:70036545-70036546	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
40	rs367854892	chr14:70036554-70036555	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
41	rs113429861	chr14:70036576-70036577	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
42	rs58198153	chr14:70036577-70036578	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
43	rs552649742	chr14:70036578-70036579	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
44	rs397965613	chr14:70036588-70036589	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
45	rs61980689	chr14:70036590-70036591	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
46	rs544007703	chr14:70036596-70036597	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
47	rs145076280	chr14:70036603-70036604	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
48	rs192739261	chr14:70036705-70036706	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
49	rs547957922	chr14:70036819-70036820	Enhancers Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
50	rs114783194	chr14:70036880-70036881	Enhancers Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	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:527 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:70027800-70036800	Weak transcription	Brain Germinal Matrix	brain
2	chr14:70029000-70036800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr14:70029000-70036800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr14:70029400-70035800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr14:70029600-70036600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr14:70034400-70036800	Weak transcription	Hela-S3	cervix
7	chr14:70034800-70036000	Enhancers	Fetal Brain Male	brain
8	chr14:70035200-70035600	Genic enhancers	Fetal Brain Female	brain
9	chr14:70035600-70036800	Strong transcription	Fetal Brain Female	brain
10	chr14:70035800-70036600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr14:70036000-70037800	Weak transcription	Fetal Brain Male	brain
12	chr14:70036600-70037400	Genic enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr14:70036600-70037400	Bivalent Enhancer	HepG2	liver
14	chr14:70036600-70039600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr14:70036600-70040200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
16	chr14:70036800-70037000	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr14:70036800-70037000	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr14:70036800-70037000	Bivalent Enhancer	Liver	Liver
19	chr14:70036800-70037200	Genic enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr14:70036800-70037400	Bivalent Enhancer	Placenta	Placenta
21	chr14:70036800-70037600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr14:70036800-70037600	Genic enhancers	Fetal Brain Female	brain
23	chr14:70036800-70037800	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr14:70036800-70038000	Enhancers	Hela-S3	cervix
25	chr14:70036800-70038400	Strong transcription	Brain Germinal Matrix	brain
26	chr14:70037000-70038200	Weak transcription	Gastric	stomach
27	chr14:70037200-70037600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr14:70037200-70039600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
29	chr14:70037400-70039600	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr14:70037400-70040200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
31	chr14:70037600-70038000	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr14:70037600-70038000	Strong transcription	Fetal Brain Female	brain
33	chr14:70037600-70039000	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr14:70037600-70039600	Bivalent Enhancer	Placenta	Placenta
35	chr14:70037800-70038000	Bivalent Enhancer	Fetal Intestine Large	intestine
36	chr14:70037800-70038200	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
37	chr14:70037800-70038200	Bivalent Enhancer	Colonic Mucosa	Colon
38	chr14:70037800-70038200	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
39	chr14:70037800-70038200	Bivalent Enhancer	Stomach Smooth Muscle	stomach
40	chr14:70037800-70038600	Bivalent Enhancer	Fetal Muscle Leg	muscle
41	chr14:70037800-70039600	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr14:70037800-70040200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
43	chr14:70037800-70040400	Enhancers	Fetal Brain Male	brain
44	chr14:70038000-70038200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr14:70038000-70038200	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr14:70038000-70038200	Bivalent Enhancer	Fetal Stomach	stomach
47	chr14:70038000-70038200	Bivalent Enhancer	Ovary	ovary
48	chr14:70038000-70038200	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
49	chr14:70038000-70038400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr14:70038000-70038400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin

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