Variant report

Variant	nsv566190
Chromosome Location	chr14:105773028-105780983
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	ATF3	chr14:105780701-105780901	K562	blood:	n/a	n/a
2	BHLHE40	chr14:105780749-105780943	GM12878	blood:	n/a	n/a
3	CCNT2	chr14:105780628-105781015	K562	blood:	n/a	n/a
4	CEBPB	chr14:105773598-105773756	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPD	chr14:105780640-105780906	HepG2	liver:	n/a	n/a
6	CHD2	chr14:105780643-105780936	GM12878	blood:	n/a	n/a
7	CHD2	chr14:105780621-105781022	Hela-S3	cervix:	n/a	n/a
8	CHD2	chr14:105780426-105780462	H1-hESC	embryonic stem cell:	n/a	n/a
9	CHD2	chr14:105778308-105778412	H1-hESC	embryonic stem cell:	n/a	n/a
10	CREB1	chr14:105780289-105781183	HepG2	liver:	n/a	n/a
11	CREB1	chr14:105780630-105781137	A549	lung:	n/a	n/a
12	CTCF	chr14:105775740-105775890	NHEK	skin:	n/a	chr14:105775880-105775888
13	CTCF	chr14:105780341-105780524	GM12892	blood:	n/a	n/a
14	CTCF	chr14:105775700-105775850	MCF-7	breast:	n/a	n/a
15	CTCF	chr14:105780482-105780493	GM19240	blood:	n/a	n/a
16	CTCF	chr14:105780474-105780478	GM19240	blood:	n/a	n/a
17	CTCF	chr14:105775720-105775870	SAEC	small airway:	n/a	n/a
18	CTCF	chr14:105780300-105780450	HepG2	liver:	n/a	n/a
19	CTCF	chr14:105780280-105780430	GM12878	blood:	n/a	n/a
20	CTCF	chr14:105780240-105780390	AG10803	skin:	n/a	n/a
21	CTCF	chr14:105780360-105780510	GM12871	blood:	n/a	n/a
22	CTCF	chr14:105780360-105780510	GM12869	blood:	n/a	n/a
23	CTCF	chr14:105775768-105775825	MCF-7	breast:	n/a	n/a
24	CTCF	chr14:105775740-105775890	HMEC	breast:	n/a	chr14:105775880-105775888
25	CTCF	chr14:105780360-105780510	GM12873	blood:	n/a	n/a
26	CTCF	chr14:105780340-105780490	GM12871	blood:	n/a	n/a
27	CTCF	chr14:105780320-105780470	SK-N-SH_RA	brain:	n/a	n/a
28	CTCF	chr14:105780340-105780490	GM06990	blood:	n/a	n/a
29	CTCF	chr14:105780375-105780470	Spleen_OC	spleen:	n/a	n/a
30	CTCF	chr14:105780380-105780530	AG04449	skin:	n/a	n/a
31	CTCF	chr14:105780420-105780570	GM12872	blood:	n/a	n/a
32	CTCF	chr14:105780440-105780590	HMEC	breast:	n/a	n/a
33	CTCF	chr14:105775780-105775857	MCF-7	breast:	n/a	n/a
34	CTCF	chr14:105780320-105780470	Caco-2	colon:	n/a	n/a
35	CTCF	chr14:105775700-105775850	HMEC	breast:	n/a	n/a
36	CTCF	chr14:105780340-105780481	GM12891	blood:	n/a	n/a
37	CTCF	chr14:105780480-105780630	GM12867	blood:	n/a	n/a
38	CTCF	chr14:105780359-105780463	GM19240	blood:	n/a	n/a
39	CTCF	chr14:105780340-105780490	GM12864	blood:	n/a	n/a
40	E2F1	chr14:105780689-105781446	Hela-S3	cervix:	n/a	chr14:105780863-105780872 chr14:105780896-105780910 chr14:105780962-105780972 chr14:105780829-105780838
41	E2F4	chr14:105780066-105780256	MCF10A-Er-Src	breast:	n/a	n/a
42	E2F4	chr14:105780701-105781027	MCF10A-Er-Src	breast:	n/a	chr14:105780863-105780872 chr14:105780896-105780910 chr14:105780962-105780972 chr14:105780829-105780838
43	E2F6	chr14:105780249-105780974	A549	lung:	n/a	chr14:105780612-105780621 chr14:105780863-105780872 chr14:105780647-105780654 chr14:105780644-105780655 chr14:105780647-105780654 chr14:105780896-105780910 chr14:105780962-105780972 chr14:105780612-105780624 chr14:105780647-105780654 chr14:105780643-105780655 chr14:105780426-105780436 chr14:105780829-105780838
44	E2F6	chr14:105780475-105780974	K562	blood:	n/a	chr14:105780612-105780621 chr14:105780863-105780872 chr14:105780647-105780654 chr14:105780644-105780655 chr14:105780647-105780654 chr14:105780896-105780910 chr14:105780962-105780972 chr14:105780612-105780624 chr14:105780647-105780654 chr14:105780643-105780655 chr14:105780829-105780838
45	E2F6	chr14:105780446-105780876	H1-hESC	embryonic stem cell:	n/a	chr14:105780612-105780621 chr14:105780863-105780872 chr14:105780647-105780654 chr14:105780644-105780655 chr14:105780647-105780654 chr14:105780612-105780624 chr14:105780647-105780654 chr14:105780643-105780655 chr14:105780829-105780838
46	E2F6	chr14:105780299-105781235	K562	blood:	n/a	chr14:105780612-105780621 chr14:105780863-105780872 chr14:105780647-105780654 chr14:105780644-105780655 chr14:105780647-105780654 chr14:105780896-105780910 chr14:105780962-105780972 chr14:105780612-105780624 chr14:105780647-105780654 chr14:105780643-105780655 chr14:105780426-105780436 chr14:105780829-105780838
47	E2F6	chr14:105780276-105780842	A549	lung:	n/a	chr14:105780612-105780621 chr14:105780647-105780654 chr14:105780644-105780655 chr14:105780647-105780654 chr14:105780612-105780624 chr14:105780647-105780654 chr14:105780643-105780655 chr14:105780426-105780436 chr14:105780829-105780838
48	E2F6	chr14:105780295-105781012	K562	blood:	n/a	chr14:105780612-105780621 chr14:105780863-105780872 chr14:105780647-105780654 chr14:105780644-105780655 chr14:105780647-105780654 chr14:105780896-105780910 chr14:105780962-105780972 chr14:105780612-105780624 chr14:105780647-105780654 chr14:105780643-105780655 chr14:105780426-105780436 chr14:105780829-105780838
49	E2F6	chr14:105780202-105780932	H1-hESC	embryonic stem cell:	n/a	chr14:105780612-105780621 chr14:105780863-105780872 chr14:105780647-105780654 chr14:105780644-105780655 chr14:105780647-105780654 chr14:105780896-105780910 chr14:105780612-105780624 chr14:105780647-105780654 chr14:105780643-105780655 chr14:105780426-105780436 chr14:105780829-105780838
50	ELF1	chr14:105780627-105780985	GM12878	blood:	n/a	chr14:105780933-105780942 chr14:105780928-105780940

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:105780137-105780187	AG09309	skin:	n/a
2	chr14:105780137-105780187	AG09309	skin:	n/a
3	chr14:105779826-105779876	GM12891	blood:	n/a
4	chr14:105780431-105780481	ECC-1	luminal epithelium:	n/a
5	chr14:105779952-105780002	HPAEpiC	pulmonary alveolar:	n/a
6	chr14:105779794-105779844	HCPEpiC	choroid plexus:	n/a
7	chr14:105779952-105780002	GM12892	blood:	n/a
8	chr14:105778041-105778091	HNPCEpiC	eye:	n/a
9	chr14:105779952-105780002	NH-A	brain:	n/a
10	chr14:105779952-105780002	SAEC	small airway:	n/a
11	chr14:105780695-105780745	BJ	skin:	n/a
12	chr14:105780695-105780745	HRE	kidney:	n/a
13	chr14:105779826-105779876	HNPCEpiC	eye:	n/a
14	chr14:105779826-105779876	IMR90	lung:	fetal
15	chr14:105779794-105779844	Caco-2	colon:	n/a
16	chr14:105779532-105779582	AG09309	skin:	n/a
17	chr14:105779532-105779582	Jurkat	blood:	n/a
18	chr14:105779952-105780002	HCPEpiC	choroid plexus:	n/a
19	chr14:105779826-105779876	SK-N-SH_RA	brain:	n/a
20	chr14:105780695-105780745	AG09319	gingival:	n/a
21	chr14:105778041-105778091	SKMC	muscle:	n/a
22	chr14:105780340-105780390	MCF-7	breast:	n/a
23	chr14:105780137-105780187	HRPEpiC	eye:	n/a
24	chr14:105780431-105780481	U87	brain:	n/a
25	chr14:105780695-105780745	HL-60	blood:	n/a
26	chr14:105779532-105779582	HUVEC	blood vessel:	n/a
27	chr14:105779826-105779876	RPTEC	kidney:	n/a
28	chr14:105779532-105779582	SK-N-MC	brain:	n/a
29	chr14:105779952-105780002	SK-N-MC	brain:	n/a
30	chr14:105780340-105780390	AG10803	skin:	n/a
31	chr14:105779952-105780002	HRE	kidney:	n/a
32	chr14:105780431-105780481	PrEC	prostate:	n/a
33	chr14:105780340-105780390	IMR90	lung:	fetal
34	chr14:105778041-105778091	SK-N-SH	brain:	n/a
35	chr14:105780340-105780390	Hela-S3	cervix:	n/a
36	chr14:105778041-105778091	PrEC	prostate:	n/a
37	chr14:105779532-105779582	MCF10A-Er-Src	breast:	n/a
38	chr14:105780420-105780470	CMK	blood:	n/a
39	chr14:105780431-105780481	BE2_C	brain:	n/a
40	chr14:105779952-105780002	BE2_C	brain:	n/a
41	chr14:105779794-105779844	HEK293	kidney:	embryo
42	chr14:105778041-105778091	GM12892	blood:	n/a
43	chr14:105779826-105779876	PANC-1	pancreas:	n/a
44	chr14:105780695-105780745	RPTEC	kidney:	n/a
45	chr14:105779952-105780002	GM19239	blood:	n/a
46	chr14:105779826-105779876	HEK293	kidney:	embryo
47	chr14:105779826-105779876	GM12892	blood:	n/a
48	chr14:105779794-105779844	HRE	kidney:	n/a
49	chr14:105779826-105779876	AG10803	skin:	n/a
50	chr14:105779910-105779960	HIPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:105778405..105782273-chr14:105864844..105868439,3	K562	blood:
2	chr14:105772029..105773588-chr14:105805773..105807669,2	MCF-7	breast:
3	chr14:105765347..105769450-chr14:105769470..105773842,3	K562	blood:
4	chr14:105647226..105648734-chr14:105780236..105782314,2	MCF-7	breast:
5	chr14:105764803..105767774-chr14:105775791..105777351,2	K562	blood:
6	chr14:105776327..105778746-chr14:105779695..105781652,2	K562	blood:
7	chr14:105765347..105769263-chr14:105769470..105773685,4	K562	blood:
8	chr14:105632643..105634203-chr14:105776322..105778030,2	K562	blood:
9	chr14:105772730..105775550-chr14:105777915..105781526,4	K562	blood:
10	chr14:105765307..105769571-chr14:105774220..105784135,13	K562	blood:
11	chr14:105765282..105769482-chr14:105778355..105784135,18	K562	blood:
12	chr14:105647019..105649589-chr14:105780411..105782070,2	MCF-7	breast:
13	chr14:105779526..105781902-chr14:105955293..105957927,2	MCF-7	breast:

Variant related genes	Relation type
PACS2	TF binding region
PACS2	CpG island
ENSG00000226174	chromatin interactions
ENSG00000179364	chromatin interactions
ENSG00000185024	chromatin interactions
ENSG00000185347	chromatin interactions
ENSG00000183828	chromatin interactions
ENSG00000257622	chromatin interactions

Extended variants
information (count: 240 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:240 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10147674	chr14:105773028-105773029	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs181547967	chr14:105773035-105773036	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs587649623	chr14:105773096-105773097	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs587713062	chr14:105773100-105773101	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs587608406	chr14:105773245-105773246	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs139551764	chr14:105773285-105773286	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs149702340	chr14:105773286-105773287	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs587617470	chr14:105773371-105773372	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs201039478	chr14:105773374-105773375	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs186206083	chr14:105773450-105773451	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs587692951	chr14:105773453-105773454	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs371938874	chr14:105773513-105773514	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs116565256	chr14:105773536-105773537	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs587628197	chr14:105773537-105773538	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs587680996	chr14:105773607-105773608	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs587737383	chr14:105773608-105773609	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs190139152	chr14:105773641-105773642	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs587694059	chr14:105773661-105773662	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs145502200	chr14:105773721-105773722	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs115795916	chr14:105773823-105773824	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs587700673	chr14:105773831-105773832	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs367552236	chr14:105773834-105773835	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs587652689	chr14:105773842-105773843	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs587709684	chr14:105773876-105773877	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs587612248	chr14:105773986-105773987	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs587666106	chr14:105774035-105774036	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs145021392	chr14:105774069-105774070	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs147552484	chr14:105774074-105774075	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs587692636	chr14:105774126-105774127	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs587727098	chr14:105774177-105774178	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs141859169	chr14:105774204-105774205	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs373674611	chr14:105774289-105774290	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs147106300	chr14:105774392-105774393	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs587616454	chr14:105774434-105774435	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs587673421	chr14:105774435-105774436	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs587746950	chr14:105774453-105774454	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs114256868	chr14:105774501-105774502	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs587719898	chr14:105774517-105774518	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs587693371	chr14:105774522-105774523	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs587754973	chr14:105774523-105774524	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs151093452	chr14:105774554-105774555	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs4983601	chr14:105774563-105774564	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs183320554	chr14:105774674-105774675	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs150226195	chr14:105774676-105774677	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs28814629	chr14:105774724-105774725	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs587737856	chr14:105774727-105774728	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs587770799	chr14:105774732-105774733	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs187456801	chr14:105774761-105774762	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs375257652	chr14:105774799-105774800	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs587703639	chr14:105774804-105774805	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	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
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Cancer	20164920	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Biliary cancer	19435499	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	20139093	CNVD
Hepatocellular carcinoma	16750200	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Glioblastoma multiforme	21922591	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian cancer	22174824	CNVD
Non-small cell lung cancer	18320023	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Congenital heart defect	22367666	CNVD
Developmental delay	22367666	CNVD
Genitourinary abnormalities	22367666	CNVD
Intellectual disability	22367666	CNVD
Microcephaly	22367666	CNVD
Muscularhypotonia	22367666	CNVD
Ocular coloboma	22367666	CNVD
Teratozoospermia	22367666	CNVD
Cervical cancer	21062161	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	21990379	CNVD
Breast cancer	16417655	CNVD
22q11 deletion syndrome	22511897	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Schizophrenia	21399695	CNVD
Intracranial ependymoma	16609018	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
14q deletion syndrome	22511897	CNVD
Epilepsy	22083797	CNVD
Ovarian cancer	21720365	CNVD
Cancer	17440070	CNVD
Neurocytoma	17123091	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Central neurocytomas	17123091	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Lung cancer	17086460	CNVD
Mortal	21835882	CNVD
small cell lung cancer	17426248	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Williams Syndrome	20824207	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Schizophrenia	23813976	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Recurrent pregnancy loss	19789632	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Breast cancer	20369283	CNVD

Chromatin state (count:471 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105768200-105775200	Weak transcription	HMEC	breast
2	chr14:105768200-105775400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr14:105768200-105775600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr14:105768200-105775600	Weak transcription	NHEK	skin
5	chr14:105768200-105777600	Weak transcription	Brain Cingulate Gyrus	brain
6	chr14:105768200-105778000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr14:105768200-105778000	Weak transcription	Brain Anterior Caudate	brain
8	chr14:105768200-105778000	Weak transcription	Brain Substantia Nigra	brain
9	chr14:105768200-105778000	Weak transcription	Fetal Stomach	stomach
10	chr14:105768200-105778000	Weak transcription	Right Ventricle	heart
11	chr14:105768200-105778000	Weak transcription	Stomach Smooth Muscle	stomach
12	chr14:105768200-105778800	Weak transcription	Fetal Lung	lung
13	chr14:105768200-105779400	Weak transcription	Colonic Mucosa	Colon
14	chr14:105768200-105779400	Weak transcription	Thymus	Thymus
15	chr14:105768200-105779600	Weak transcription	GM12878-XiMat	blood
16	chr14:105768200-105779800	Weak transcription	NHLF	lung
17	chr14:105768200-105780000	Weak transcription	NHDF-Ad	bronchial
18	chr14:105768200-105780200	Weak transcription	Gastric	stomach
19	chr14:105768200-105780200	Weak transcription	Right Atrium	heart
20	chr14:105768400-105773400	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr14:105768400-105777600	Weak transcription	Brain Hippocampus Middle	brain
22	chr14:105768400-105777800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr14:105768400-105778000	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr14:105768400-105779200	Weak transcription	Skeletal Muscle Female	skeletal muscle
25	chr14:105768400-105779400	Weak transcription	Skeletal Muscle Male	skeletal muscle
26	chr14:105768400-105779800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr14:105768400-105779800	Weak transcription	Lung	lung
28	chr14:105768400-105780200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr14:105770600-105775800	Weak transcription	Pancreas	Pancrea
30	chr14:105770800-105779600	Weak transcription	Rectal Mucosa Donor 29	rectum
31	chr14:105771400-105780200	Weak transcription	Sigmoid Colon	Sigmoid Colon
32	chr14:105771600-105780000	Weak transcription	K562	blood
33	chr14:105772000-105774200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr14:105772200-105773600	Weak transcription	Rectal Mucosa Donor 31	rectum
35	chr14:105772200-105774200	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr14:105772200-105778200	Weak transcription	Fetal Muscle Trunk	muscle
37	chr14:105772200-105779800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
38	chr14:105772200-105780000	Weak transcription	Primary T cells from cord blood	blood
39	chr14:105772400-105778200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr14:105772400-105779400	Weak transcription	Spleen	Spleen
41	chr14:105772400-105779800	Weak transcription	Primary T cells fromperipheralblood	blood
42	chr14:105772400-105779800	Weak transcription	Primary T helper cells fromperipheralblood	blood
43	chr14:105772600-105773600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr14:105772600-105773600	Weak transcription	Fetal Intestine Small	intestine
45	chr14:105772600-105778200	Weak transcription	Fetal Muscle Leg	muscle
46	chr14:105772600-105779400	Weak transcription	Fetal Thymus	thymus
47	chr14:105772800-105774200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr14:105773000-105773600	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr14:105773000-105774200	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr14:105773200-105774000	Enhancers	HUES64 Cell Line	embryonic stem cell

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