Variant report

Variant	nsv566188
Chromosome Location	chr14:105771428-105780920
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	chr14:105780621-105781022	Hela-S3	cervix:	n/a	n/a
7	CHD2	chr14:105780643-105780936	GM12878	blood:	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	chr14:105780630-105781137	A549	lung:	n/a	n/a
11	CREB1	chr14:105780289-105781183	HepG2	liver:	n/a	n/a
12	CTCF	chr14:105780340-105780490	GM06990	blood:	n/a	n/a
13	CTCF	chr14:105775700-105775850	HMEC	breast:	n/a	n/a
14	CTCF	chr14:105780360-105780510	GM12871	blood:	n/a	n/a
15	CTCF	chr14:105780360-105780510	GM12869	blood:	n/a	n/a
16	CTCF	chr14:105780320-105780470	SK-N-SH_RA	brain:	n/a	n/a
17	CTCF	chr14:105780341-105780524	GM12892	blood:	n/a	n/a
18	CTCF	chr14:105780340-105780490	GM12871	blood:	n/a	n/a
19	CTCF	chr14:105780480-105780630	GM12867	blood:	n/a	n/a
20	CTCF	chr14:105780375-105780470	Spleen_OC	spleen:	n/a	n/a
21	CTCF	chr14:105775780-105775857	MCF-7	breast:	n/a	n/a
22	CTCF	chr14:105780340-105780481	GM12891	blood:	n/a	n/a
23	CTCF	chr14:105780300-105780450	HepG2	liver:	n/a	n/a
24	CTCF	chr14:105780359-105780463	GM19240	blood:	n/a	n/a
25	CTCF	chr14:105780240-105780390	AG10803	skin:	n/a	n/a
26	CTCF	chr14:105780360-105780510	GM12873	blood:	n/a	n/a
27	CTCF	chr14:105780482-105780493	GM19240	blood:	n/a	n/a
28	CTCF	chr14:105780474-105780478	GM19240	blood:	n/a	n/a
29	CTCF	chr14:105780440-105780590	HMEC	breast:	n/a	n/a
30	CTCF	chr14:105780320-105780470	Caco-2	colon:	n/a	n/a
31	CTCF	chr14:105775768-105775825	MCF-7	breast:	n/a	n/a
32	CTCF	chr14:105780280-105780430	GM12878	blood:	n/a	n/a
33	CTCF	chr14:105780420-105780570	GM12872	blood:	n/a	n/a
34	CTCF	chr14:105775740-105775890	NHEK	skin:	n/a	chr14:105775880-105775888
35	CTCF	chr14:105775700-105775850	MCF-7	breast:	n/a	n/a
36	CTCF	chr14:105775740-105775890	HMEC	breast:	n/a	chr14:105775880-105775888
37	CTCF	chr14:105780340-105780490	GM12864	blood:	n/a	n/a
38	CTCF	chr14:105775720-105775870	SAEC	small airway:	n/a	n/a
39	CTCF	chr14:105780380-105780530	AG04449	skin:	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	chr14:105780446-105780876	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
44	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
45	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
46	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
47	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
48	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
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	chr14:105780591-105780995	K562	blood:	n/a	chr14:105780933-105780942 chr14:105780928-105780940

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:105780431-105780481	HPAEpiC	pulmonary alveolar:	n/a
2	chr14:105780431-105780481	HPAEpiC	pulmonary alveolar:	n/a
3	chr14:105780431-105780481	GM12878	blood:	n/a
4	chr14:105780420-105780470	HCM	heart:	n/a
5	chr14:105780695-105780745	NB4	blood:	n/a
6	chr14:105779532-105779582	T-47D	breast:	n/a
7	chr14:105779952-105780002	SAEC	small airway:	n/a
8	chr14:105779794-105779844	Jurkat	blood:	n/a
9	chr14:105780420-105780470	MCF10A-Er-Src	breast:	n/a
10	chr14:105780340-105780390	U87	brain:	n/a
11	chr14:105771879-105771929	U87	brain:	n/a
12	chr14:105778041-105778091	IMR90	lung:	fetal
13	chr14:105779826-105779876	HNPCEpiC	eye:	n/a
14	chr14:105780420-105780470	Hepatocyte	liver:	n/a
15	chr14:105779826-105779876	GM12892	blood:	n/a
16	chr14:105780431-105780481	HEEpiC	esophagus:	n/a
17	chr14:105771879-105771929	Jurkat	blood:	n/a
18	chr14:105779910-105779960	HIPEpiC	eye:	n/a
19	chr14:105780137-105780187	HRPEpiC	eye:	n/a
20	chr14:105780340-105780390	HRPEpiC	eye:	n/a
21	chr14:105771879-105771929	GM12892	blood:	n/a
22	chr14:105780695-105780745	HCPEpiC	choroid plexus:	n/a
23	chr14:105780420-105780470	K562	blood:	n/a
24	chr14:105771879-105771929	ProgFib	skin:	n/a
25	chr14:105779794-105779844	K562	blood:	n/a
26	chr14:105780137-105780187	ECC-1	luminal epithelium:	n/a
27	chr14:105780431-105780481	Hela-S3	cervix:	n/a
28	chr14:105780137-105780187	K562	blood:	n/a
29	chr14:105780340-105780390	PFSK-1	brain:	n/a
30	chr14:105780431-105780481	SK-N-SH_RA	brain:	n/a
31	chr14:105779794-105779844	Hepatocyte	liver:	n/a
32	chr14:105779794-105779844	HPAEpiC	pulmonary alveolar:	n/a
33	chr14:105780695-105780745	HRPEpiC	eye:	n/a
34	chr14:105771879-105771929	GM12878	blood:	n/a
35	chr14:105779532-105779582	HMEC	breast:	n/a
36	chr14:105779952-105780002	SKMC	muscle:	n/a
37	chr14:105771879-105771929	NHBE	bronchial:	n/a
38	chr14:105778041-105778091	PrEC	prostate:	n/a
39	chr14:105780431-105780481	ProgFib	skin:	n/a
40	chr14:105778041-105778091	GM06990	blood:	n/a
41	chr14:105779952-105780002	Hela-S3	cervix:	n/a
42	chr14:105779952-105780002	SK-N-SH_RA	brain:	n/a
43	chr14:105779952-105780002	LNCaP	prostate:	n/a
44	chr14:105779532-105779582	HPAEpiC	pulmonary alveolar:	n/a
45	chr14:105780431-105780481	A549	lung:	n/a
46	chr14:105780137-105780187	AG09319	gingival:	n/a
47	chr14:105780340-105780390	T-47D	breast:	n/a
48	chr14:105779952-105780002	ProgFib	skin:	n/a
49	chr14:105771879-105771929	T-47D	breast:	n/a
50	chr14:105778041-105778091	HCT-116	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:105765282..105769482-chr14:105778355..105784135,18	K562	blood:
2	chr14:105765347..105769450-chr14:105769470..105773842,3	K562	blood:
3	chr14:105647226..105648734-chr14:105780236..105782314,2	MCF-7	breast:
4	chr14:105778405..105782273-chr14:105864844..105868439,3	K562	blood:
5	chr14:105779526..105781902-chr14:105955293..105957927,2	MCF-7	breast:
6	chr14:105770409..105772942-chr14:105807785..105809717,2	MCF-7	breast:
7	chr14:105647019..105649589-chr14:105780411..105782070,2	MCF-7	breast:
8	chr14:105632643..105634203-chr14:105776322..105778030,2	K562	blood:
9	chr14:105764803..105767774-chr14:105775791..105777351,2	K562	blood:
10	chr14:105772730..105775550-chr14:105777915..105781526,4	K562	blood:
11	chr14:105772029..105773588-chr14:105805773..105807669,2	MCF-7	breast:
12	chr14:105776327..105778746-chr14:105779695..105781652,2	K562	blood:
13	chr14:105765307..105769571-chr14:105774220..105784135,13	K562	blood:
14	chr14:105765347..105769263-chr14:105769470..105773685,4	K562	blood:

Variant related genes	Relation type
BRF1	TF binding region
PACS2	TF binding region
BRF1	CpG island
PACS2	CpG island
ENSG00000183828	chromatin interactions
ENSG00000179364	chromatin interactions
ENSG00000185347	chromatin interactions
ENSG00000185024	chromatin interactions
ENSG00000257622	chromatin interactions
ENSG00000226174	chromatin interactions

Extended variants
information (count: 298 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:298 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12100543	chr14:105771428-105771429	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs375783035	chr14:105771513-105771514	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs587756943	chr14:105771530-105771531	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs587615749	chr14:105771543-105771544	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs114011668	chr14:105771566-105771567	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs61996224	chr14:105771649-105771650	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs375621901	chr14:105771677-105771678	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs375096770	chr14:105771718-105771719	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs77997443	chr14:105771753-105771754	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs142914488	chr14:105771763-105771764	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs587747906	chr14:105771829-105771830	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs192069864	chr14:105771864-105771865	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs587647247	chr14:105771967-105771968	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs149593780	chr14:105771976-105771977	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs587605493	chr14:105771983-105771984	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs184467310	chr14:105772022-105772023	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs188475767	chr14:105772041-105772042	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs75264897	chr14:105772055-105772056	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs587675486	chr14:105772066-105772067	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs76732584	chr14:105772219-105772220	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs587625796	chr14:105772246-105772247	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs148307625	chr14:105772247-105772248	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs181500835	chr14:105772248-105772249	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs113705671	chr14:105772268-105772269	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs141402842	chr14:105772283-105772284	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs587776065	chr14:105772301-105772302	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs370454499	chr14:105772308-105772309	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs587643872	chr14:105772329-105772330	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs370896869	chr14:105772330-105772331	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs146286629	chr14:105772331-105772332	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs185825134	chr14:105772412-105772413	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs139400564	chr14:105772468-105772469	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs74515425	chr14:105772564-105772565	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs587763461	chr14:105772567-105772568	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs181934432	chr14:105772593-105772594	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs587720663	chr14:105772602-105772603	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs587735956	chr14:105772624-105772625	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs368099287	chr14:105772625-105772626	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs587668472	chr14:105772629-105772630	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs587671379	chr14:105772699-105772700	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs587706165	chr14:105772709-105772710	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs187384797	chr14:105772739-105772740	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs587677954	chr14:105772749-105772750	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs142617367	chr14:105772765-105772766	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs191197153	chr14:105772802-105772803	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs587688985	chr14:105772823-105772824	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs75265595	chr14:105772840-105772841	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs587764542	chr14:105772862-105772863	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs10135289	chr14:105772875-105772876	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs587721339	chr14:105772952-105772953	Weak transcription Enhancers	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:533 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105768200-105771600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr14:105768200-105771600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
3	chr14:105768200-105771800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr14:105768200-105771800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
5	chr14:105768200-105771800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr14:105768200-105771800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr14:105768200-105775200	Weak transcription	HMEC	breast
8	chr14:105768200-105775400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr14:105768200-105775600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr14:105768200-105775600	Weak transcription	NHEK	skin
11	chr14:105768200-105777600	Weak transcription	Brain Cingulate Gyrus	brain
12	chr14:105768200-105778000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr14:105768200-105778000	Weak transcription	Brain Anterior Caudate	brain
14	chr14:105768200-105778000	Weak transcription	Brain Substantia Nigra	brain
15	chr14:105768200-105778000	Weak transcription	Fetal Stomach	stomach
16	chr14:105768200-105778000	Weak transcription	Right Ventricle	heart
17	chr14:105768200-105778000	Weak transcription	Stomach Smooth Muscle	stomach
18	chr14:105768200-105778800	Weak transcription	Fetal Lung	lung
19	chr14:105768200-105779400	Weak transcription	Colonic Mucosa	Colon
20	chr14:105768200-105779400	Weak transcription	Thymus	Thymus
21	chr14:105768200-105779600	Weak transcription	GM12878-XiMat	blood
22	chr14:105768200-105779800	Weak transcription	NHLF	lung
23	chr14:105768200-105780000	Weak transcription	NHDF-Ad	bronchial
24	chr14:105768200-105780200	Weak transcription	Gastric	stomach
25	chr14:105768200-105780200	Weak transcription	Right Atrium	heart
26	chr14:105768400-105771600	Weak transcription	Primary hematopoietic stem cells	blood
27	chr14:105768400-105771600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
28	chr14:105768400-105771800	Weak transcription	Fetal Intestine Large	intestine
29	chr14:105768400-105771800	Weak transcription	Fetal Intestine Small	intestine
30	chr14:105768400-105771800	Weak transcription	Spleen	Spleen
31	chr14:105768400-105772000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr14:105768400-105772000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr14:105768400-105772000	Weak transcription	Fetal Muscle Leg	muscle
34	chr14:105768400-105772200	Weak transcription	Dnd41	blood
35	chr14:105768400-105773400	Weak transcription	H1 Cell Line	embryonic stem cell
36	chr14:105768400-105777600	Weak transcription	Brain Hippocampus Middle	brain
37	chr14:105768400-105777800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
38	chr14:105768400-105778000	Weak transcription	Brain Inferior Temporal Lobe	brain
39	chr14:105768400-105779200	Weak transcription	Skeletal Muscle Female	skeletal muscle
40	chr14:105768400-105779400	Weak transcription	Skeletal Muscle Male	skeletal muscle
41	chr14:105768400-105779800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
42	chr14:105768400-105779800	Weak transcription	Lung	lung
43	chr14:105768400-105780200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr14:105769000-105771800	Weak transcription	HepG2	liver
45	chr14:105769200-105772000	Weak transcription	Fetal Muscle Trunk	muscle
46	chr14:105769400-105771600	Weak transcription	Primary monocytes fromperipheralblood	blood
47	chr14:105769400-105771600	Weak transcription	Monocytes-CD14+_RO01746	blood
48	chr14:105770000-105771600	Enhancers	K562	blood
49	chr14:105770600-105771800	Weak transcription	HUES6 Cell Line	embryonic stem cell
50	chr14:105770600-105772000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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