Variant report

Variant	nsv832886
Chromosome Location	chr14:105571958-105606663
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:170)
CpG islands
(count:672)
Chromatin interactive
region (count:32)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:170 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr14:105597533-105598007	HCT-116	colon:	n/a	n/a
2	CBX3	chr14:105606276-105606713	K562	blood:	n/a	n/a
3	CBX3	chr14:105597490-105598063	HCT-116	colon:	n/a	n/a
4	CBX3	chr14:105606324-105606692	K562	blood:	n/a	n/a
5	CEBPB	chr14:105571686-105571988	A549	lung:	n/a	chr14:105571827-105571838
6	CEBPB	chr14:105584857-105585623	MCF-7	breast:	n/a	n/a
7	CEBPB	chr14:105585152-105585236	HepG2	liver:	n/a	n/a
8	CEBPB	chr14:105585012-105585717	MCF-7	breast:	n/a	n/a
9	CEBPB	chr14:105571665-105571991	HepG2	liver:	n/a	chr14:105571827-105571838
10	CEBPB	chr14:105574819-105575115	HepG2	liver:	n/a	chr14:105574978-105574989
11	CEBPB	chr14:105602020-105602475	A549	lung:	n/a	chr14:105602218-105602229
12	CEBPB	chr14:105602202-105602233	H1-hESC	embryonic stem cell:	n/a	chr14:105602218-105602229
13	CEBPB	chr14:105602051-105602404	K562	blood:	n/a	chr14:105602218-105602229
14	CEBPB	chr14:105571629-105572041	A549	lung:	n/a	chr14:105571827-105571838
15	CEBPB	chr14:105574845-105575152	A549	lung:	n/a	chr14:105574978-105574989
16	CEBPB	chr14:105602145-105602475	MCF-7	breast:	n/a	chr14:105602218-105602229
17	CEBPB	chr14:105602053-105602402	A549	lung:	n/a	chr14:105602218-105602229
18	CEBPB	chr14:105602070-105602404	HepG2	liver:	n/a	chr14:105602218-105602229
19	CEBPB	chr14:105571670-105572007	IMR90	lung:	n/a	chr14:105571827-105571838
20	CEBPB	chr14:105602082-105602324	Hela-S3	cervix:	n/a	chr14:105602218-105602229
21	CEBPB	chr14:105574958-105575149	H1-hESC	embryonic stem cell:	n/a	chr14:105574978-105574989
22	CEBPB	chr14:105602049-105602403	IMR90	lung:	n/a	chr14:105602218-105602229
23	CREB1	chr14:105603330-105603686	K562	blood:	n/a	n/a
24	CTCF	chr14:105586180-105586330	GM06990	blood:	n/a	n/a
25	CTCF	chr14:105584340-105584490	GM12874	blood:	n/a	n/a
26	CTCF	chr14:105586120-105586270	MCF-7	breast:	n/a	chr14:105586136-105586145
27	CTCF	chr14:105586020-105586170	NHEK	skin:	n/a	chr14:105586136-105586145 chr14:105586102-105586115
28	CTCF	chr14:105574340-105574490	GM12873	blood:	n/a	n/a
29	CTCF	chr14:105585508-105585646	MCF-7	breast:	n/a	n/a
30	CTCF	chr14:105574360-105574510	MCF-7	breast:	n/a	n/a
31	CTCF	chr14:105585980-105586130	SAEC	small airway:	n/a	chr14:105586102-105586115
32	CTCF	chr14:105585500-105585650	HMEC	breast:	n/a	n/a
33	CTCF	chr14:105585510-105585652	MCF-7	breast:	n/a	n/a
34	CTCF	chr14:105585547-105585607	LNCaP	prostate:	n/a	n/a
35	CTCF	chr14:105574454-105574475	LNCaP	prostate:	n/a	n/a
36	CTCF	chr14:105585520-105585670	HEEpiC	esophagus:	n/a	n/a
37	CTCF	chr14:105574520-105574670	HFF	foreskin:	n/a	n/a
38	CTCF	chr14:105574380-105574530	A549	lung:	n/a	n/a
39	CTCF	chr14:105586100-105586250	GM12871	blood:	n/a	chr14:105586136-105586145 chr14:105586102-105586115
40	CTCF	chr14:105586120-105586163	NHEK	skin:	n/a	chr14:105586136-105586145
41	CTCF	chr14:105574440-105574590	HMF	breast:	n/a	n/a
42	CTCF	chr14:105603903-105604018	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr14:105592700-105592850	NHEK	skin:	n/a	chr14:105592711-105592724
44	CTCF	chr14:105603849-105604026	HepG2	liver:	n/a	n/a
45	CTCF	chr14:105603960-105604110	HepG2	liver:	n/a	chr14:105604072-105604085
46	CTCF	chr14:105585502-105585658	NHEK	skin:	n/a	n/a
47	CTCF	chr14:105585560-105585710	MCF-7	breast:	n/a	n/a
48	CTCF	chr14:105585500-105585650	NHEK	skin:	n/a	n/a
49	CTCF	chr14:105574340-105574490	HPF	lung:	n/a	n/a
50	CTCF	chr14:105585534-105585613	MCF-7	breast:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:105582624-105582674	Hela-S3	cervix:	n/a
2	chr14:105582624-105582674	Hela-S3	cervix:	n/a
3	chr14:105581043-105581093	BJ	skin:	n/a
4	chr14:105603986-105604036	MCF10A-Er-Src	breast:	n/a
5	chr14:105582624-105582674	NHBE	bronchial:	n/a
6	chr14:105576362-105576412	HEK293	kidney:	embryo
7	chr14:105581043-105581093	HUVEC	blood vessel:	n/a
8	chr14:105605750-105605800	GM19239	blood:	n/a
9	chr14:105576362-105576412	HEEpiC	esophagus:	n/a
10	chr14:105603153-105603203	NT2-D1	testis:	n/a
11	chr14:105603986-105604036	MCF-7	breast:	n/a
12	chr14:105603460-105603510	PFSK-1	brain:	n/a
13	chr14:105605750-105605800	ECC-1	luminal epithelium:	n/a
14	chr14:105576362-105576412	HepG2	liver:	n/a
15	chr14:105600994-105601044	BE2_C	brain:	n/a
16	chr14:105581043-105581093	U87	brain:	n/a
17	chr14:105603389-105603439	H1-hESC	embryonic stem cell:	embryo
18	chr14:105581043-105581093	PrEC	prostate:	n/a
19	chr14:105605750-105605800	GM12891	blood:	n/a
20	chr14:105603389-105603439	SAEC	small airway:	n/a
21	chr14:105603460-105603510	MCF10A-Er-Src	breast:	n/a
22	chr14:105600994-105601044	SAEC	small airway:	n/a
23	chr14:105600994-105601044	AG09309	skin:	n/a
24	chr14:105605750-105605800	K562	blood:	n/a
25	chr14:105582624-105582674	LNCaP	prostate:	n/a
26	chr14:105605750-105605800	PFSK-1	brain:	n/a
27	chr14:105605750-105605800	NHBE	bronchial:	n/a
28	chr14:105603460-105603510	GM12891	blood:	n/a
29	chr14:105600994-105601044	HPAEpiC	pulmonary alveolar:	n/a
30	chr14:105603460-105603510	K562	blood:	n/a
31	chr14:105603153-105603203	T-47D	breast:	n/a
32	chr14:105603153-105603203	AG09309	skin:	n/a
33	chr14:105603389-105603439	GM06990	blood:	n/a
34	chr14:105603460-105603510	BE2_C	brain:	n/a
35	chr14:105584224-105584274	HAEpiC	amniotic membrane:	n/a
36	chr14:105603460-105603510	T-47D	breast:	n/a
37	chr14:105584462-105584512	NH-A	brain:	n/a
38	chr14:105582624-105582674	Jurkat	blood:	n/a
39	chr14:105603389-105603439	CMK	blood:	n/a
40	chr14:105603153-105603203	MCF-7	breast:	n/a
41	chr14:105603389-105603439	IMR90	lung:	fetal
42	chr14:105584224-105584274	GM12892	blood:	n/a
43	chr14:105584462-105584512	LNCaP	prostate:	n/a
44	chr14:105584224-105584274	Hepatocyte	liver:	n/a
45	chr14:105600994-105601044	HRCEpiC	kidney:	n/a
46	chr14:105603389-105603439	T-47D	breast:	n/a
47	chr14:105600994-105601044	AoSMC	blood vessel:	n/a
48	chr14:105584462-105584512	GM12892	blood:	n/a
49	chr14:105582624-105582674	SK-N-SH_RA	brain:	n/a
50	chr14:105603460-105603510	Jurkat	blood:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:105567323..105568937-chr14:105583984..105585803,2	MCF-7	breast:
2	chr14:105567398..105568987-chr14:105582432..105584780,2	MCF-7	breast:
3	chr14:105567450..105569151-chr14:105572022..105574911,2	K562	blood:
4	chr14:105602588..105606045-chr14:105617930..105622124,4	MCF-7	breast:
5	chr14:105605892..105608252-chr14:105621955..105625449,3	K562	blood:
6	chr14:105553187..105555561-chr14:105589136..105591325,2	MCF-7	breast:
7	chr14:105601373..105604174-chr14:105610785..105613135,3	MCF-7	breast:
8	chr14:105586207..105587794-chr14:105595383..105596914,2	MCF-7	breast:
9	chr14:105581813..105588921-chr14:105589522..105595491,7	MCF-7	breast:
10	chr14:105556660..105559437-chr14:105588253..105590015,2	MCF-7	breast:
11	chr14:105584495..105586972-chr14:105646028..105648252,2	MCF-7	breast:
12	chr14:105599383..105601359-chr14:105605338..105607216,2	MCF-7	breast:
13	chr14:105556860..105558487-chr14:105603973..105605818,2	K562	blood:
14	chr14:105605939..105608674-chr14:105628049..105630309,2	K562	blood:
15	chr14:105581813..105588921-chr14:105589522..105595491,7	MCF-7	breast:
16	chr14:105571300..105574874-chr14:105580786..105584672,4	MCF-7	breast:
17	chr14:105583616..105585913-chr14:105629918..105634007,5	MCF-7	breast:
18	chr14:105605014..105607392-chr14:105623375..105626287,2	K562	blood:
19	chr14:105557976..105560807-chr14:105572239..105574036,2	MCF-7	breast:
20	chr14:105597394..105599153-chr14:105603205..105605036,2	K562	blood:
21	chr14:105603768..105606019-chr14:105630363..105631971,2	K562	blood:
22	chr14:105448909..105450840-chr14:105583708..105586505,2	MCF-7	breast:
23	chr14:105606160..105607990-chr14:105612669..105614397,2	MCF-7	breast:
24	chr14:105603827..105606395-chr14:105610368..105612251,2	MCF-7	breast:
25	chr14:105597394..105599153-chr14:105603205..105605036,2	K562	blood:
26	chr14:105584234..105586859-chr14:105605626..105608481,2	MCF-7	breast:
27	chr14:105584234..105586859-chr14:105605626..105608481,2	MCF-7	breast:
28	chr14:105585474..105587655-chr14:105643859..105645608,2	MCF-7	breast:
29	chr14:105586207..105587794-chr14:105595383..105596914,2	MCF-7	breast:
30	chr14:105563166..105566144-chr14:105593732..105596034,2	MCF-7	breast:
31	chr14:105599383..105601359-chr14:105605338..105607216,2	MCF-7	breast:
32	chr14:105571300..105574874-chr14:105580786..105584672,4	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000258154	TF binding region
ENSG00000258154	CpG island
ENSG00000257622	chromatin interactions
ENSG00000183828	chromatin interactions
ENSG00000257556	chromatin interactions
ENSG00000184916	chromatin interactions

Extended variants
information (count: 1184 )
Associated
traits (count: 112 )

Variant overlapped rSNPs/rCNVs (count:1184 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs115650375	chr14:105572269-105572270	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs375616469	chr14:105572307-105572308	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs55723653	chr14:105572340-105572341	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs587604316	chr14:105572418-105572419	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs57824859	chr14:105572440-105572441	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs587739411	chr14:105572496-105572497	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs367932568	chr14:105572506-105572507	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs4983583	chr14:105572539-105572540	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs182290585	chr14:105572564-105572565	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs587649766	chr14:105572619-105572620	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs587686176	chr14:105572654-105572655	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs373824153	chr14:105572697-105572698	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs28893237	chr14:105572705-105572706	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs374595109	chr14:105572712-105572713	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs8018607	chr14:105572749-105572750	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs185016314	chr14:105572759-105572760	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs587757098	chr14:105572874-105572875	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs149706268	chr14:105572913-105572914	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs191573238	chr14:105572982-105572983	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs145516453	chr14:105573024-105573025	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs111540838	chr14:105573156-105573157	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs587646998	chr14:105573166-105573167	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs148425949	chr14:105573167-105573168	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs199648535	chr14:105573190-105573191	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs201566614	chr14:105573191-105573192	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs10566597	chr14:105573192-105573193	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs76849565	chr14:105573195-105573196	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs587660536	chr14:105573223-105573224	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs77540655	chr14:105573297-105573298	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs587596782	chr14:105573446-105573447	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs587693124	chr14:105573497-105573498	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs117582307	chr14:105573504-105573505	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs587649835	chr14:105573578-105573579	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs10129625	chr14:105573654-105573655	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs587743589	chr14:105573672-105573673	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs182971410	chr14:105573759-105573760	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs150925437	chr14:105573858-105573859	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs112209824	chr14:105573859-105573860	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs188069881	chr14:105573863-105573864	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs587634554	chr14:105573870-105573871	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs117324349	chr14:105573877-105573878	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs192917408	chr14:105573934-105573935	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs8004326	chr14:105573973-105573974	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs587699445	chr14:105574001-105574002	Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs587763149	chr14:105574006-105574007	Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs144522314	chr14:105574010-105574011	Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs8003024	chr14:105574020-105574021	Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs587615111	chr14:105574024-105574025	Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs587695115	chr14:105574027-105574028	Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs587731494	chr14:105574063-105574064	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:112)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Recurrent pregnancy loss	19789632	CNVD
Aortic dissecting aneurysms	22263138	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD
Breast cancer	22522925	CNVD
Oligozoospermia	20877625	CNVD
Sertoli-cell only syndrome	20877625	CNVD
Ovarian clear cell carcinoma	21343371	CNVD

Chromatin state (count:151 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105574000-105574200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
2	chr14:105574000-105576800	Weak transcription	Right Atrium	heart
3	chr14:105574600-105575000	Enhancers	A549	lung
4	chr14:105576200-105576400	Enhancers	Esophagus	oesophagus
5	chr14:105576400-105581200	Weak transcription	Esophagus	oesophagus
6	chr14:105578400-105578800	Active TSS	HSMM	muscle
7	chr14:105581000-105581800	Enhancers	NHEK	skin
8	chr14:105581200-105582200	Enhancers	Esophagus	oesophagus
9	chr14:105581400-105581800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr14:105581800-105584600	Weak transcription	NHEK	skin
11	chr14:105581800-105584800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr14:105582200-105584400	Weak transcription	Esophagus	oesophagus
13	chr14:105582400-105582600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr14:105583200-105588000	Enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr14:105584400-105585200	Enhancers	Esophagus	oesophagus
16	chr14:105584400-105586800	Enhancers	HMEC	breast
17	chr14:105584600-105585200	Enhancers	Placenta Amnion	Placenta Amnion
18	chr14:105584600-105585600	Enhancers	NHEK	skin
19	chr14:105584600-105586800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr14:105584800-105586400	Enhancers	Placenta	Placenta
21	chr14:105584800-105586400	Enhancers	Fetal Thymus	thymus
22	chr14:105584800-105586800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr14:105584800-105586800	Enhancers	Pancreas	Pancrea
24	chr14:105584800-105587000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr14:105585000-105585800	Enhancers	Primary hematopoietic stem cells	blood
26	chr14:105585000-105586000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr14:105585000-105586200	Enhancers	Gastric	stomach
28	chr14:105585200-105585600	Weak transcription	Placenta Amnion	Placenta Amnion
29	chr14:105585200-105585800	Weak transcription	Esophagus	oesophagus
30	chr14:105585200-105586200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr14:105585200-105586200	Enhancers	Stomach Mucosa	stomach
32	chr14:105585400-105586400	Bivalent Enhancer	Fetal Muscle Leg	muscle
33	chr14:105585600-105585800	Bivalent Enhancer	Colonic Mucosa	Colon
34	chr14:105585600-105586000	Flanking Active TSS	NHEK	skin
35	chr14:105585600-105586200	Bivalent/Poised TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr14:105585600-105586400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
37	chr14:105585600-105586600	Enhancers	Placenta Amnion	Placenta Amnion
38	chr14:105585800-105586800	Enhancers	Esophagus	oesophagus
39	chr14:105586000-105586200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr14:105586000-105587000	Enhancers	NHEK	skin
41	chr14:105586800-105587800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr14:105587800-105588200	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr14:105588000-105592800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
44	chr14:105589000-105590400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr14:105589200-105590400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr14:105589400-105590000	Enhancers	Duodenum Mucosa	Duodenum
47	chr14:105589800-105590800	Enhancers	Fetal Brain Male	brain
48	chr14:105590000-105590400	Enhancers	Rectal Mucosa Donor 29	rectum
49	chr14:105590000-105590800	Flanking Active TSS	Duodenum Mucosa	Duodenum
50	chr14:105590200-105590600	Enhancers	Brain Inferior Temporal Lobe	brain

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