Variant report

Variant	nsv902429
Chromosome Location	chr14:105564734-105602619
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:213)
CpG islands
(count:366)
Chromatin interactive
region (count:31)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:213 , 50 per page) page: 1 2 3 4 5

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	chr14:105597490-105598063	HCT-116	colon:	n/a	n/a
3	CEBPB	chr14:105584857-105585623	MCF-7	breast:	n/a	n/a
4	CEBPB	chr14:105602020-105602475	A549	lung:	n/a	chr14:105602218-105602229
5	CEBPB	chr14:105574819-105575115	HepG2	liver:	n/a	chr14:105574978-105574989
6	CEBPB	chr14:105571696-105571902	K562	blood:	n/a	chr14:105571827-105571838
7	CEBPB	chr14:105602202-105602233	H1-hESC	embryonic stem cell:	n/a	chr14:105602218-105602229
8	CEBPB	chr14:105602070-105602404	HepG2	liver:	n/a	chr14:105602218-105602229
9	CEBPB	chr14:105585012-105585717	MCF-7	breast:	n/a	n/a
10	CEBPB	chr14:105602082-105602324	Hela-S3	cervix:	n/a	chr14:105602218-105602229
11	CEBPB	chr14:105602051-105602404	K562	blood:	n/a	chr14:105602218-105602229
12	CEBPB	chr14:105602145-105602475	MCF-7	breast:	n/a	chr14:105602218-105602229
13	CEBPB	chr14:105602049-105602403	IMR90	lung:	n/a	chr14:105602218-105602229
14	CEBPB	chr14:105602053-105602402	A549	lung:	n/a	chr14:105602218-105602229
15	CEBPB	chr14:105574958-105575149	H1-hESC	embryonic stem cell:	n/a	chr14:105574978-105574989
16	CEBPB	chr14:105571629-105572041	A549	lung:	n/a	chr14:105571827-105571838
17	CEBPB	chr14:105574845-105575152	A549	lung:	n/a	chr14:105574978-105574989
18	CEBPB	chr14:105571693-105571913	H1-hESC	embryonic stem cell:	n/a	chr14:105571827-105571838
19	CEBPB	chr14:105571665-105571991	HepG2	liver:	n/a	chr14:105571827-105571838
20	CEBPB	chr14:105571686-105571988	A549	lung:	n/a	chr14:105571827-105571838
21	CEBPB	chr14:105585152-105585236	HepG2	liver:	n/a	n/a
22	CEBPB	chr14:105571670-105572007	IMR90	lung:	n/a	chr14:105571827-105571838
23	CTCF	chr14:105586080-105586230	SAEC	small airway:	n/a	chr14:105586136-105586145 chr14:105586102-105586115
24	CTCF	chr14:105574360-105574510	AG10803	skin:	n/a	n/a
25	CTCF	chr14:105567371-105567448	GM19238	blood:	n/a	n/a
26	CTCF	chr14:105567360-105567468	NHEK	skin:	n/a	n/a
27	CTCF	chr14:105585534-105585613	MCF-7	breast:	n/a	n/a
28	CTCF	chr14:105574400-105574550	HEEpiC	esophagus:	n/a	n/a
29	CTCF	chr14:105592700-105592850	NHEK	skin:	n/a	chr14:105592711-105592724
30	CTCF	chr14:105574460-105574610	MCF-7	breast:	n/a	n/a
31	CTCF	chr14:105574340-105574490	HPF	lung:	n/a	n/a
32	CTCF	chr14:105585502-105585658	NHEK	skin:	n/a	n/a
33	CTCF	chr14:105585560-105585710	MCF-7	breast:	n/a	n/a
34	CTCF	chr14:105585480-105585630	SAEC	small airway:	n/a	n/a
35	CTCF	chr14:105586180-105586330	GM06990	blood:	n/a	n/a
36	CTCF	chr14:105585380-105585530	MCF-7	breast:	n/a	n/a
37	CTCF	chr14:105585980-105586130	SAEC	small airway:	n/a	chr14:105586102-105586115
38	CTCF	chr14:105567345-105567476	GM12891	blood:	n/a	n/a
39	CTCF	chr14:105574440-105574590	HMF	breast:	n/a	n/a
40	CTCF	chr14:105567395-105567415	MCF-7	breast:	n/a	n/a
41	CTCF	chr14:105567368-105567442	MCF-7	breast:	n/a	n/a
42	CTCF	chr14:105567395-105567425	MCF-7	breast:	n/a	n/a
43	CTCF	chr14:105585500-105585650	NHEK	skin:	n/a	n/a
44	CTCF	chr14:105574454-105574475	LNCaP	prostate:	n/a	n/a
45	CTCF	chr14:105585508-105585646	MCF-7	breast:	n/a	n/a
46	CTCF	chr14:105567380-105567530	HRE	kidney:	n/a	n/a
47	CTCF	chr14:105585507-105585660	MCF-7	breast:	n/a	n/a
48	CTCF	chr14:105586120-105586163	NHEK	skin:	n/a	chr14:105586136-105586145
49	CTCF	chr14:105585531-105585626	MCF-7	breast:	n/a	n/a
50	CTCF	chr14:105574340-105574490	GM12873	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:105584462-105584512	GM19239	blood:	n/a
2	chr14:105584224-105584274	GM12892	blood:	n/a
3	chr14:105584224-105584274	Hepatocyte	liver:	n/a
4	chr14:105582624-105582674	BE2_C	brain:	n/a
5	chr14:105582624-105582674	HEK293	kidney:	embryo
6	chr14:105581043-105581093	PFSK-1	brain:	n/a
7	chr14:105584224-105584274	NHDF-neo	bronchial:	n/a
8	chr14:105584462-105584512	BJ	skin:	n/a
9	chr14:105582624-105582674	AG09319	gingival:	n/a
10	chr14:105584462-105584512	NB4	blood:	n/a
11	chr14:105600994-105601044	HRPEpiC	eye:	n/a
12	chr14:105600994-105601044	AG09319	gingival:	n/a
13	chr14:105576362-105576412	SK-N-MC	brain:	n/a
14	chr14:105584462-105584512	AoSMC	blood vessel:	n/a
15	chr14:105582624-105582674	GM12878	blood:	n/a
16	chr14:105576362-105576412	IMR90	lung:	fetal
17	chr14:105581043-105581093	Caco-2	colon:	n/a
18	chr14:105584224-105584274	ECC-1	luminal epithelium:	n/a
19	chr14:105584224-105584274	GM12891	blood:	n/a
20	chr14:105582624-105582674	NB4	blood:	n/a
21	chr14:105600994-105601044	GM19239	blood:	n/a
22	chr14:105581043-105581093	NT2-D1	testis:	n/a
23	chr14:105582624-105582674	H1-hESC	embryonic stem cell:	embryo
24	chr14:105584224-105584274	PFSK-1	brain:	n/a
25	chr14:105581043-105581093	AoSMC	blood vessel:	n/a
26	chr14:105584462-105584512	HCM	heart:	n/a
27	chr14:105582624-105582674	AoSMC	blood vessel:	n/a
28	chr14:105581043-105581093	T-47D	breast:	n/a
29	chr14:105576362-105576412	HCPEpiC	choroid plexus:	n/a
30	chr14:105576362-105576412	SK-N-SH	brain:	n/a
31	chr14:105584462-105584512	MCF10A-Er-Src	breast:	n/a
32	chr14:105584462-105584512	GM12892	blood:	n/a
33	chr14:105581043-105581093	ProgFib	skin:	n/a
34	chr14:105600994-105601044	CMK	blood:	n/a
35	chr14:105581043-105581093	GM12891	blood:	n/a
36	chr14:105584462-105584512	NT2-D1	testis:	n/a
37	chr14:105576362-105576412	NHBE	bronchial:	n/a
38	chr14:105584224-105584274	HUVEC	blood vessel:	n/a
39	chr14:105584224-105584274	BJ	skin:	n/a
40	chr14:105600994-105601044	HUVEC	blood vessel:	n/a
41	chr14:105584462-105584512	HPAEpiC	pulmonary alveolar:	n/a
42	chr14:105600994-105601044	MCF10A-Er-Src	breast:	n/a
43	chr14:105584462-105584512	AG10803	skin:	n/a
44	chr14:105584224-105584274	HPAEpiC	pulmonary alveolar:	n/a
45	chr14:105581043-105581093	HRPEpiC	eye:	n/a
46	chr14:105581043-105581093	HL-60	blood:	n/a
47	chr14:105582624-105582674	U87	brain:	n/a
48	chr14:105584462-105584512	K562	blood:	n/a
49	chr14:105582624-105582674	HEEpiC	esophagus:	n/a
50	chr14:105582624-105582674	A549	lung:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:105599383..105601359-chr14:105605338..105607216,2	MCF-7	breast:
2	chr14:105586207..105587794-chr14:105595383..105596914,2	MCF-7	breast:
3	chr14:105560177..105564340-chr14:105567752..105570620,3	K562	blood:
4	chr14:105557976..105560807-chr14:105572239..105574036,2	MCF-7	breast:
5	chr14:105556660..105559437-chr14:105588253..105590015,2	MCF-7	breast:
6	chr14:105448909..105450840-chr14:105583708..105586505,2	MCF-7	breast:
7	chr14:105567398..105568987-chr14:105582432..105584780,2	MCF-7	breast:
8	chr14:105583616..105585913-chr14:105629918..105634007,5	MCF-7	breast:
9	chr14:105585474..105587655-chr14:105643859..105645608,2	MCF-7	breast:
10	chr14:105597394..105599153-chr14:105603205..105605036,2	K562	blood:
11	chr14:105563166..105566144-chr14:105593732..105596034,2	MCF-7	breast:
12	chr14:105586207..105587794-chr14:105595383..105596914,2	MCF-7	breast:
13	chr14:105567714..105569852-chr14:105645987..105647633,2	MCF-7	breast:
14	chr14:105567450..105569151-chr14:105572022..105574911,2	K562	blood:
15	chr14:105584234..105586859-chr14:105605626..105608481,2	MCF-7	breast:
16	chr14:105566584..105569448-chr14:105610028..105612847,2	MCF-7	breast:
17	chr14:105601373..105604174-chr14:105610785..105613135,3	MCF-7	breast:
18	chr14:105602588..105606045-chr14:105617930..105622124,4	MCF-7	breast:
19	chr14:105571300..105574874-chr14:105580786..105584672,4	MCF-7	breast:
20	chr14:105584495..105586972-chr14:105646028..105648252,2	MCF-7	breast:
21	chr14:105568093..105570383-chr14:105666909..105669878,2	K562	blood:
22	chr14:105567450..105569151-chr14:105572022..105574911,2	K562	blood:
23	chr14:105567323..105568937-chr14:105583984..105585803,2	MCF-7	breast:
24	chr14:105567323..105568937-chr14:105583984..105585803,2	MCF-7	breast:
25	chr14:105563166..105566144-chr14:105593732..105596034,2	MCF-7	breast:
26	chr14:105553187..105555561-chr14:105589136..105591325,2	MCF-7	breast:
27	chr14:105581813..105588921-chr14:105589522..105595491,7	MCF-7	breast:
28	chr14:105571300..105574874-chr14:105580786..105584672,4	MCF-7	breast:
29	chr14:105265265..105267697-chr14:105564443..105566490,2	MCF-7	breast:
30	chr14:105581813..105588921-chr14:105589522..105595491,7	MCF-7	breast:
31	chr14:105567398..105568987-chr14:105582432..105584780,2	MCF-7	breast:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C14orf79-2	chr14:105565056-105565227	NR_110546
2	lnc-C14orf79-2	chr14:105565381-105565468	XLOC_010952
3	lnc-C14orf79-2	chr14:105564810-105564910	NR_110546
4	lnc-C14orf79-2	chr14:105564810-105564853	NONHSAT040321
5	lnc-C14orf79-2	chr14:105565381-105565891	XLOC_010952
6	lnc-C14orf79-2	chr14:105564810-105565172	XLOC_010952
7	lnc-C14orf79-2	chr14:105565056-105565341	ENSG00000257556
8	lnc-C14orf79-2	chr14:105565090-105565227	XLOC_010952
9	lnc-C14orf79-2	chr14:105565619-105565833	NR_110546
10	lnc-C14orf79-2	chr14:105564810-105564823	XLOC_010952
11	lnc-C14orf79-2	chr14:105564810-105564910	ENSG00000257556

No data

Variant related genes	Relation type
ENSG00000258154	TF binding region
ENSG00000258154	CpG island
ENSG00000179627	chromatin interactions
ENSG00000257556	chromatin interactions
ENSG00000257622	chromatin interactions
ENSG00000183828	chromatin interactions
ECHDC1	miRNA target sites
MBD6	miRNA target sites
COPS3	miRNA target sites
MBD1	miRNA target sites

Extended variants
information (count: 1269 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:1269 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7160811	chr14:105564734-105564735	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs74896861	chr14:105564740-105564741	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs587702083	chr14:105564833-105564834	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs190744839	chr14:105564852-105564853	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs587615531	chr14:105564853-105564854	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs138368991	chr14:105564882-105564883	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs587749563	chr14:105564896-105564897	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs587673051	chr14:105564927-105564928	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs587729620	chr14:105564948-105564949	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs587774529	chr14:105564966-105564967	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
11	rs587659962	chr14:105564990-105564991	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs587723040	chr14:105565034-105565035	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
13	rs200281481	chr14:105565038-105565039	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs10686748	chr14:105565040-105565041	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs36071292	chr14:105565041-105565042	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
16	rs201117035	chr14:105565042-105565043	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
17	rs199758183	chr14:105565047-105565048	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
18	rs35878899	chr14:105565048-105565049	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
19	rs587598503	chr14:105565050-105565051	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
20	rs142834956	chr14:105565055-105565056	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
21	rs371444259	chr14:105565057-105565058	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
22	rs182022170	chr14:105565087-105565088	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
23	rs587612583	chr14:105565168-105565169	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
24	rs587712365	chr14:105565183-105565184	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
25	rs150623594	chr14:105565195-105565196	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
26	rs184633651	chr14:105565208-105565209	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
27	rs587626528	chr14:105565325-105565326	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
28	rs587653725	chr14:105565331-105565332	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
29	rs587737481	chr14:105565349-105565350	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs587608762	chr14:105565372-105565373	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs188267057	chr14:105565476-105565477	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
32	rs139701187	chr14:105565508-105565509	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
33	rs587647859	chr14:105565525-105565526	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
34	rs587705304	chr14:105565538-105565539	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
35	rs4983580	chr14:105565542-105565543	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs587664222	chr14:105565553-105565554	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
37	rs587693300	chr14:105565566-105565567	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
38	rs587755231	chr14:105565579-105565580	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
39	rs375412664	chr14:105565596-105565597	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
40	rs587649698	chr14:105565599-105565600	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
41	rs77169789	chr14:105565616-105565617	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
42	rs587714694	chr14:105565658-105565659	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
43	rs587611242	chr14:105565660-105565661	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
44	rs149343209	chr14:105565684-105565685	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
45	rs11621606	chr14:105565770-105565771	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs587606626	chr14:105565839-105565840	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
47	rs587644504	chr14:105565895-105565896	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs587638578	chr14:105565900-105565901	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs587658673	chr14:105565907-105565908	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs587734120	chr14:105565909-105565910	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:111)

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
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD
Oligozoospermia	20877625	CNVD
Sertoli-cell only syndrome	20877625	CNVD

Chromatin state (count:137 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105561000-105565000	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr14:105561000-105567800	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr14:105561200-105565400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr14:105562400-105565400	Weak transcription	A549	lung
5	chr14:105564200-105564800	Weak transcription	Fetal Intestine Small	intestine
6	chr14:105564600-105565000	Weak transcription	Esophagus	oesophagus
7	chr14:105564600-105568800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr14:105565000-105565200	Enhancers	Esophagus	oesophagus
9	chr14:105565000-105566000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr14:105565200-105566000	Weak transcription	Esophagus	oesophagus
11	chr14:105566000-105566200	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr14:105566000-105566400	ZNF genes & repeats	Esophagus	oesophagus
13	chr14:105566000-105566600	ZNF genes & repeats	GM12878-XiMat	blood
14	chr14:105566200-105566400	Weak transcription	NHEK	skin
15	chr14:105566200-105566600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr14:105566400-105566800	Weak transcription	Esophagus	oesophagus
17	chr14:105566600-105567400	Weak transcription	GM12878-XiMat	blood
18	chr14:105566600-105570000	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr14:105566800-105567200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr14:105566800-105567400	Enhancers	Esophagus	oesophagus
21	chr14:105567200-105567600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr14:105567400-105567800	Enhancers	GM12878-XiMat	blood
23	chr14:105567400-105568800	Weak transcription	Esophagus	oesophagus
24	chr14:105568400-105569800	Enhancers	NHEK	skin
25	chr14:105568600-105569200	Enhancers	HMEC	breast
26	chr14:105568800-105569000	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr14:105568800-105569600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr14:105568800-105569600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr14:105568800-105569600	Enhancers	Esophagus	oesophagus
30	chr14:105569000-105569600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr14:105569000-105571400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr14:105569200-105569600	Bivalent Enhancer	GM12878-XiMat	blood
33	chr14:105569600-105570000	Enhancers	GM12878-XiMat	blood
34	chr14:105571600-105571800	Bivalent Enhancer	Primary T cells from cord blood	blood
35	chr14:105571600-105571800	Flanking Bivalent TSS/Enh	Rectal Mucosa Donor 31	rectum
36	chr14:105574000-105574200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
37	chr14:105574000-105576800	Weak transcription	Right Atrium	heart
38	chr14:105574600-105575000	Enhancers	A549	lung
39	chr14:105576200-105576400	Enhancers	Esophagus	oesophagus
40	chr14:105576400-105581200	Weak transcription	Esophagus	oesophagus
41	chr14:105578400-105578800	Active TSS	HSMM	muscle
42	chr14:105581000-105581800	Enhancers	NHEK	skin
43	chr14:105581200-105582200	Enhancers	Esophagus	oesophagus
44	chr14:105581400-105581800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr14:105581800-105584600	Weak transcription	NHEK	skin
46	chr14:105581800-105584800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr14:105582200-105584400	Weak transcription	Esophagus	oesophagus
48	chr14:105582400-105582600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr14:105583200-105588000	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr14:105584400-105585200	Enhancers	Esophagus	oesophagus

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