Variant report

Variant	nsv456114
Chromosome Location	chr13:110742919-110761521
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:110747028-110747378	HepG2	liver:	n/a	n/a
2	ATF3	chr13:110747004-110747394	HepG2	liver:	n/a	n/a
3	ATF3	chr13:110746807-110747587	HCT-116	colon:	n/a	n/a
4	ATF3	chr13:110746851-110747571	HCT-116	colon:	n/a	n/a
5	BATF	chr13:110747066-110747290	GM12878	blood:	n/a	n/a
6	BCL11A	chr13:110748572-110748854	GM12878	blood:	n/a	n/a
7	BCL3	chr13:110760679-110761348	GM12878	blood:	n/a	n/a
8	BCL3	chr13:110760593-110761387	GM12878	blood:	n/a	n/a
9	BHLHE40	chr13:110749085-110749089	GM12878	blood:	n/a	n/a
10	BHLHE40	chr13:110761395-110761569	GM12878	blood:	n/a	n/a
11	BHLHE40	chr13:110746972-110747519	HepG2	liver:	n/a	n/a
12	BRCA1	chr13:110761462-110761478	HepG2	liver:	n/a	n/a
13	BRCA1	chr13:110746877-110747579	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr13:110746778-110747630	HCT-116	colon:	n/a	n/a
15	CBX3	chr13:110746760-110747617	HCT-116	colon:	n/a	n/a
16	CEBPB	chr13:110746804-110747400	ECC-1	luminal epithelium:	n/a	chr13:110747051-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747064
17	CEBPB	chr13:110746889-110747256	K562	blood:	n/a	chr13:110747051-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747064
18	CEBPB	chr13:110746753-110747461	MCF-7	breast:	n/a	chr13:110747051-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747064
19	CEBPB	chr13:110755830-110756439	HCT-116	colon:	n/a	chr13:110755918-110755926
20	CEBPB	chr13:110746939-110747219	K562	blood:	n/a	chr13:110747051-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747064
21	CEBPB	chr13:110756097-110756102	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr13:110746873-110747420	HepG2	liver:	n/a	chr13:110747051-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747064
23	CEBPB	chr13:110746856-110747774	HepG2	liver:	n/a	chr13:110747051-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747064
24	CEBPB	chr13:110746859-110747712	HepG2	liver:	n/a	chr13:110747051-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747064
25	CEBPB	chr13:110746909-110747425	A549	lung:	n/a	chr13:110747051-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747064
26	CEBPB	chr13:110746584-110747728	HCT-116	colon:	n/a	chr13:110747051-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747064
27	CEBPB	chr13:110746760-110747477	A549	lung:	n/a	chr13:110747051-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747064
28	CEBPB	chr13:110746921-110747366	HepG2	liver:	n/a	chr13:110747051-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747064
29	CEBPB	chr13:110746838-110747467	IMR90	lung:	n/a	chr13:110747051-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747064
30	CEBPB	chr13:110746865-110747393	A549	lung:	n/a	chr13:110747051-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747064
31	CEBPB	chr13:110746811-110747480	MCF-7	breast:	n/a	chr13:110747051-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747064
32	CEBPB	chr13:110756017-110756125	HepG2	liver:	n/a	n/a
33	CEBPB	chr13:110746845-110747558	Hela-S3	cervix:	n/a	chr13:110747051-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747064
34	CEBPB	chr13:110746882-110747118	K562	blood:	n/a	chr13:110747051-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747064
35	CEBPB	chr13:110746879-110747245	H1-hESC	embryonic stem cell:	n/a	chr13:110747051-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747064
36	CEBPB	chr13:110746570-110747628	HCT-116	colon:	n/a	chr13:110747051-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747064
37	CEBPB	chr13:110753343-110753483	HepG2	liver:	n/a	n/a
38	CEBPB	chr13:110746781-110747515	ECC-1	luminal epithelium:	n/a	chr13:110747051-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747062 chr13:110747053-110747064
39	CEBPD	chr13:110746873-110747323	HepG2	liver:	n/a	chr13:110747053-110747062 chr13:110747052-110747063
40	CEBPD	chr13:110746880-110747431	HepG2	liver:	n/a	chr13:110747053-110747062 chr13:110747052-110747063
41	CHD1	chr13:110760988-110761761	IMR90	lung:	n/a	n/a
42	CHD2	chr13:110761306-110761693	Hela-S3	cervix:	n/a	n/a
43	CHD2	chr13:110761077-110761512	GM12878	blood:	n/a	n/a
44	CHD2	chr13:110746983-110747416	HepG2	liver:	n/a	n/a
45	CHD2	chr13:110746870-110747440	Hela-S3	cervix:	n/a	n/a
46	CREB1	chr13:110747130-110747394	A549	lung:	n/a	n/a
47	CREB1	chr13:110747123-110747366	A549	lung:	n/a	n/a
48	CTCF	chr13:110761120-110761692	MCF-7	breast:	n/a	n/a
49	CTCF	chr13:110760560-110760710	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr13:110761303-110761568	Pancreas_OC	pancreas:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:110747452-110747502	MCF-7	breast:	n/a
2	chr13:110759424-110759474	PANC-1	pancreas:	n/a
3	chr13:110747452-110747502	HNPCEpiC	eye:	n/a
4	chr13:110747452-110747502	BJ	skin:	n/a
5	chr13:110747452-110747502	Jurkat	blood:	n/a
6	chr13:110759424-110759474	H1-hESC	embryonic stem cell:	embryo
7	chr13:110747452-110747502	A549	lung:	n/a
8	chr13:110747452-110747502	SK-N-SH	brain:	n/a
9	chr13:110759424-110759474	HUVEC	blood vessel:	n/a
10	chr13:110747452-110747502	K562	blood:	n/a
11	chr13:110759424-110759474	AG10803	skin:	n/a
12	chr13:110759424-110759474	ECC-1	luminal epithelium:	n/a
13	chr13:110759424-110759474	HCM	heart:	n/a
14	chr13:110759424-110759474	HepG2	liver:	n/a
15	chr13:110747452-110747502	RPTEC	kidney:	n/a
16	chr13:110759424-110759474	BJ	skin:	n/a
17	chr13:110759424-110759474	K562	blood:	n/a
18	chr13:110759424-110759474	HEK293	kidney:	embryo
19	chr13:110759424-110759474	AG04449	skin:	fetal
20	chr13:110759424-110759474	HRPEpiC	eye:	n/a
21	chr13:110759424-110759474	Hela-S3	cervix:	n/a
22	chr13:110759424-110759474	SK-N-SH_RA	brain:	n/a
23	chr13:110747452-110747502	HMEC	breast:	n/a
24	chr13:110759424-110759474	ProgFib	skin:	n/a
25	chr13:110759424-110759474	ovcar-3	ovarian:	n/a
26	chr13:110747452-110747502	HCF	heart:	n/a
27	chr13:110747452-110747502	AG09319	gingival:	n/a
28	chr13:110747452-110747502	Hela-S3	cervix:	n/a
29	chr13:110759424-110759474	HAEpiC	amniotic membrane:	n/a
30	chr13:110747452-110747502	HRPEpiC	eye:	n/a
31	chr13:110747452-110747502	AoSMC	blood vessel:	n/a
32	chr13:110747452-110747502	HCPEpiC	choroid plexus:	n/a
33	chr13:110747452-110747502	SAEC	small airway:	n/a
34	chr13:110747452-110747502	HCT-116	colon:	n/a
35	chr13:110747452-110747502	AG04450	lung:	fetal
36	chr13:110759424-110759474	AG09309	skin:	n/a
37	chr13:110759424-110759474	PFSK-1	brain:	n/a
38	chr13:110747452-110747502	GM12878	blood:	n/a
39	chr13:110747452-110747502	ovcar-3	ovarian:	n/a
40	chr13:110747452-110747502	ECC-1	luminal epithelium:	n/a
41	chr13:110759424-110759474	AG04450	lung:	fetal
42	chr13:110759424-110759474	IMR90	lung:	fetal
43	chr13:110759424-110759474	NHBE	bronchial:	n/a
44	chr13:110747452-110747502	BE2_C	brain:	n/a
45	chr13:110747452-110747502	SK-N-MC	brain:	n/a
46	chr13:110747452-110747502	HEEpiC	esophagus:	n/a
47	chr13:110759424-110759474	HCF	heart:	n/a
48	chr13:110747452-110747502	NHDF-neo	bronchial:	n/a
49	chr13:110759424-110759474	SK-N-MC	brain:	n/a
50	chr13:110747452-110747502	HIPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:110583476..110584263-chr13:110760363..110760981,2	MCF-7	breast:
2	chr13:110760613..110762563-chr13:110777021..110779083,2	MCF-7	breast:
3	chr13:110761020..110763183-chr13:110765963..110768234,2	MCF-7	breast:
4	chr13:110747132..110748037-chr19:48901248..48902099,2	NB4	blood:
5	chr13:109567424..109568073-chr13:110760960..110761768,2	MCF-7	breast:
6	chr13:109613700..109614457-chr13:110760895..110761419,2	MCF-7	breast:
7	chr13:110436096..110439350-chr13:110760184..110763012,5	MCF-7	breast:
8	chr13:110436205..110441713-chr13:110758837..110762777,7	MCF-7	breast:
9	chr13:110651999..110652742-chr13:110760981..110761503,2	MCF-7	breast:
10	chr13:110753728..110755942-chr13:110757866..110759784,2	K562	blood:
11	chr13:110654511..110656415-chr13:110759069..110761693,2	MCF-7	breast:
12	chr13:110651354..110653633-chr13:110756277..110757904,2	MCF-7	breast:
13	chr13:110417399..110417917-chr13:110760942..110761494,2	MCF-7	breast:
14	chr13:110742841..110744367-chr13:110745194..110747379,2	MCF-7	breast:
15	chr13:110742841..110744367-chr13:110745194..110747379,2	MCF-7	breast:
16	chr13:110753728..110755942-chr13:110757866..110759784,2	K562	blood:
17	chr13:110443953..110447179-chr13:110758507..110762069,3	MCF-7	breast:
18	chr13:110748461..110750541-chr13:110753298..110755107,2	K562	blood:
19	chr13:110717144..110719381-chr13:110752515..110754017,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COL4A1-4	chr13:110750200-110750498	NONHSAT035136

Variant related genes	Relation type
RN7SL783P	TF binding region
RN7SL783P	CpG island
ENSG00000265885	chromatin interactions
ENSG00000185950	chromatin interactions

Extended variants
information (count: 744 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:744 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7988988	chr13:110742919-110742920	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs567511212	chr13:110742950-110742951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs536548869	chr13:110742961-110742962	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs551877840	chr13:110742969-110742970	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs181755900	chr13:110742977-110742978	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs72652054	chr13:110742990-110742991	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs374188052	chr13:110742994-110742995	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs544837461	chr13:110743010-110743011	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs73622407	chr13:110743042-110743043	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs200836238	chr13:110743087-110743088	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs79938362	chr13:110743126-110743127	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs185164394	chr13:110743127-110743128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs531237695	chr13:110743139-110743140	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs540758133	chr13:110743143-110743144	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs560949264	chr13:110743156-110743157	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs373347001	chr13:110743183-110743184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs543328358	chr13:110743190-110743191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs114980869	chr13:110743220-110743221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs551231584	chr13:110743251-110743252	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs552033941	chr13:110743273-110743274	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs536060913	chr13:110743287-110743288	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs115944539	chr13:110743305-110743306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs189639610	chr13:110743348-110743349	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs547525734	chr13:110743349-110743350	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs181139024	chr13:110743375-110743376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs536215424	chr13:110743397-110743398	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs12585713	chr13:110743456-110743457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs78449871	chr13:110743471-110743472	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs567909495	chr13:110743486-110743487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs77344577	chr13:110743522-110743523	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs538543225	chr13:110743533-110743534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs79193277	chr13:110743565-110743566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs536841462	chr13:110743567-110743568	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs571867281	chr13:110743580-110743581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs1816885	chr13:110743665-110743666	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs554340856	chr13:110743670-110743671	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs117937439	chr13:110743689-110743690	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs147221940	chr13:110743713-110743714	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs11843281	chr13:110743793-110743794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs563254724	chr13:110743815-110743816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs1348618	chr13:110743816-110743817	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs545707756	chr13:110743843-110743844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs1348619	chr13:110743894-110743895	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs1348620	chr13:110743927-110743928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs202240858	chr13:110743929-110743930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs547882502	chr13:110743934-110743935	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs561257215	chr13:110743970-110743971	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs140576320	chr13:110743989-110743990	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs549954267	chr13:110744037-110744038	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs185185315	chr13:110744062-110744063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Cancer	20164919	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Myoepithelioma	18604193	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	18632612	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
Gastric cancer	17908304	CNVD
Liposarcoma	21253554	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Thyroid cancer	19087340	CNVD
abortions and stillbirths	19751515	CNVD
Acute myeloid leukemia	21251322	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Burkitt''s lymphoma	20823134	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Burkitt''s lymphoma	19759907	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Medulloblastoma	19270706	CNVD
Mental retardation	17124404	CNVD
Leukemia	18688285	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21858162	CNVD
Melanoma	17363583	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	21645411	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Breast cancer	16608533	CNVD
Glioblastoma multiforme	22286061	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
abnormal development	18461090	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Malignant glioma	17146433	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Glioma	17123091	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	20409316	CNVD
Central neurocytomas	17123091	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Neurocytoma	17123091	CNVD
Mantle cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Glioma	20126413	CNVD

Chromatin state (count:346 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:110738800-110746400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr13:110741800-110745000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr13:110742000-110746800	Weak transcription	Liver	Liver
4	chr13:110742200-110743600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr13:110742400-110746600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr13:110743000-110743400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr13:110743400-110746400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr13:110743600-110744000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr13:110744000-110745200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr13:110744800-110746400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr13:110745000-110745200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr13:110745000-110745400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr13:110745000-110746000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr13:110745000-110746800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr13:110745200-110745400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr13:110745200-110745600	Enhancers	Brain Substantia Nigra	brain
17	chr13:110745200-110745600	ZNF genes & repeats	HMEC	breast
18	chr13:110745200-110745800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr13:110745200-110746000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr13:110745200-110747400	Enhancers	Right Ventricle	heart
21	chr13:110745200-110747600	Enhancers	Rectal Smooth Muscle	rectum
22	chr13:110745200-110747800	Enhancers	Muscle Satellite Cultured Cells	--
23	chr13:110745200-110747800	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr13:110745200-110749000	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr13:110745400-110745600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr13:110745400-110746000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr13:110745400-110746400	Enhancers	Colon Smooth Muscle	Colon
28	chr13:110745400-110747800	Enhancers	Right Atrium	heart
29	chr13:110745400-110749200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr13:110745600-110745800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr13:110745600-110745800	Weak transcription	HMEC	breast
32	chr13:110745600-110746000	Weak transcription	Brain Substantia Nigra	brain
33	chr13:110745600-110746000	Enhancers	Psoas Muscle	Psoas
34	chr13:110745600-110747200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr13:110745600-110748400	Enhancers	Pancreas	Pancrea
36	chr13:110745800-110746800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr13:110745800-110746800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr13:110745800-110746800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr13:110745800-110748800	Enhancers	HMEC	breast
40	chr13:110746000-110746200	Weak transcription	Psoas Muscle	Psoas
41	chr13:110746000-110746400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr13:110746000-110746800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr13:110746000-110746800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr13:110746000-110747400	Enhancers	Brain Cingulate Gyrus	brain
45	chr13:110746000-110748400	Enhancers	Brain Substantia Nigra	brain
46	chr13:110746000-110749000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr13:110746200-110746400	Enhancers	Skeletal Muscle Male	skeletal muscle
48	chr13:110746200-110746600	Enhancers	Psoas Muscle	Psoas
49	chr13:110746200-110746600	Enhancers	Skeletal Muscle Female	skeletal muscle
50	chr13:110746200-110747000	Enhancers	Left Ventricle	heart

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