Variant report

Variant	nsv886536
Chromosome Location	chr6:110426046-110502831
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1201)
CpG islands
(count:1103)
Chromatin interactive
region (count:21)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1201 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:110500895-110501857	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:110499656-110500138	K562	blood:	n/a	chr6:110499816-110499832
3	ARID3A	chr6:110499741-110500204	HepG2	liver:	n/a	chr6:110499816-110499832
4	ARID3A	chr6:110500871-110501726	K562	blood:	n/a	n/a
5	ATF1	chr6:110501073-110501507	K562	blood:	n/a	n/a
6	ATF2	chr6:110501268-110501741	GM12878	blood:	n/a	n/a
7	ATF2	chr6:110500864-110501264	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr6:110500953-110501814	GM12878	blood:	n/a	n/a
9	ATF3	chr6:110501224-110501397	GM12878	blood:	n/a	chr6:110501258-110501267
10	BACH1	chr6:110499771-110499954	K562	blood:	n/a	n/a
11	BACH1	chr6:110499919-110501307	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCLAF1	chr6:110499722-110500200	GM12878	blood:	n/a	n/a
13	BCLAF1	chr6:110500811-110501531	GM12878	blood:	n/a	chr6:110501038-110501047 chr6:110500881-110500890 chr6:110500986-110500995
14	BCLAF1	chr6:110499842-110500317	GM12878	blood:	n/a	n/a
15	BCLAF1	chr6:110501051-110501992	GM12878	blood:	n/a	n/a
16	BHLHE40	chr6:110499776-110500251	K562	blood:	n/a	n/a
17	BHLHE40	chr6:110500738-110501772	K562	blood:	n/a	n/a
18	BHLHE40	chr6:110499781-110500434	GM12878	blood:	n/a	n/a
19	BHLHE40	chr6:110500804-110501768	GM12878	blood:	n/a	n/a
20	BHLHE40	chr6:110500684-110501734	HepG2	liver:	n/a	n/a
21	BRCA1	chr6:110500868-110501867	GM12878	blood:	n/a	n/a
22	BRCA1	chr6:110461954-110462245	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr6:110491990-110492051	H1-hESC	embryonic stem cell:	n/a	n/a
24	BRCA1	chr6:110501163-110501675	HepG2	liver:	n/a	n/a
25	BRCA1	chr6:110500753-110501756	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr6:110500939-110501639	H1-hESC	embryonic stem cell:	n/a	n/a
27	CBX3	chr6:110499744-110500168	K562	blood:	n/a	n/a
28	CBX3	chr6:110459571-110460062	K562	blood:	n/a	n/a
29	CBX3	chr6:110500669-110501824	K562	blood:	n/a	n/a
30	CCNT2	chr6:110500723-110501445	K562	blood:	n/a	chr6:110501180-110501189 chr6:110501258-110501267 chr6:110500882-110500891
31	CCNT2	chr6:110499878-110500408	K562	blood:	n/a	n/a
32	CEBPB	chr6:110500869-110501614	H1-hESC	embryonic stem cell:	n/a	chr6:110501161-110501172 chr6:110501159-110501170
33	CEBPB	chr6:110500824-110501596	ECC-1	luminal epithelium:	n/a	chr6:110501161-110501172 chr6:110501159-110501170
34	CEBPB	chr6:110500647-110501743	K562	blood:	n/a	chr6:110501161-110501172 chr6:110501159-110501170
35	CEBPB	chr6:110491404-110491557	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr6:110471137-110471384	HepG2	liver:	n/a	chr6:110471269-110471280 chr6:110471269-110471282
37	CEBPB	chr6:110461878-110462475	HCT-116	colon:	n/a	n/a
38	CEBPB	chr6:110500794-110501847	IMR90	lung:	n/a	chr6:110501161-110501172 chr6:110501159-110501170
39	CEBPB	chr6:110493350-110493627	K562	blood:	n/a	n/a
40	CEBPB	chr6:110462021-110462349	A549	lung:	n/a	n/a
41	CEBPB	chr6:110500803-110501672	K562	blood:	n/a	chr6:110501161-110501172 chr6:110501159-110501170
42	CEBPB	chr6:110493350-110493629	A549	lung:	n/a	n/a
43	CEBPB	chr6:110461935-110462388	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr6:110471106-110471379	IMR90	lung:	n/a	chr6:110471269-110471280 chr6:110471269-110471282
45	CEBPB	chr6:110493433-110493462	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr6:110500926-110501387	ECC-1	luminal epithelium:	n/a	chr6:110501161-110501172 chr6:110501159-110501170
47	CEBPB	chr6:110500645-110501879	Hela-S3	cervix:	n/a	chr6:110501161-110501172 chr6:110501159-110501170
48	CEBPB	chr6:110500981-110501292	K562	blood:	n/a	chr6:110501161-110501172 chr6:110501159-110501170
49	CEBPB	chr6:110500912-110501399	HepG2	liver:	n/a	chr6:110501161-110501172 chr6:110501159-110501170
50	CEBPB	chr6:110500815-110501801	A549	lung:	n/a	chr6:110501161-110501172 chr6:110501159-110501170

(count:1103 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:110501287-110501337	NH-A	brain:	n/a
2	chr6:110500932-110500982	MCF10A-Er-Src	breast:	n/a
3	chr6:110501706-110501756	AG04450	lung:	fetal
4	chr6:110498910-110498960	Hela-S3	cervix:	n/a
5	chr6:110500691-110500741	HCPEpiC	choroid plexus:	n/a
6	chr6:110501287-110501337	NH-A	brain:	n/a
7	chr6:110500932-110500982	MCF10A-Er-Src	breast:	n/a
8	chr6:110501706-110501756	AG04450	lung:	fetal
9	chr6:110498910-110498960	Hela-S3	cervix:	n/a
10	chr6:110500691-110500741	HCPEpiC	choroid plexus:	n/a
11	chr6:110501610-110501660	Jurkat	blood:	n/a
12	chr6:110500990-110501040	T-47D	breast:	n/a
13	chr6:110501372-110501422	HepG2	liver:	n/a
14	chr6:110500390-110500440	HepG2	liver:	n/a
15	chr6:110500990-110501040	SK-N-SH	brain:	n/a
16	chr6:110500337-110500387	HCT-116	colon:	n/a
17	chr6:110501077-110501127	PFSK-1	brain:	n/a
18	chr6:110500390-110500440	A549	lung:	n/a
19	chr6:110501899-110501949	HRE	kidney:	n/a
20	chr6:110501627-110501677	Hela-S3	cervix:	n/a
21	chr6:110501287-110501337	AG09319	gingival:	n/a
22	chr6:110501899-110501949	A549	lung:	n/a
23	chr6:110500390-110500440	H1-hESC	embryonic stem cell:	embryo
24	chr6:110501353-110501403	SKMC	muscle:	n/a
25	chr6:110501281-110501331	SK-N-MC	brain:	n/a
26	chr6:110501706-110501756	HRCEpiC	kidney:	n/a
27	chr6:110500932-110500982	NHDF-neo	bronchial:	n/a
28	chr6:110501353-110501403	GM12892	blood:	n/a
29	chr6:110426718-110426768	NHBE	bronchial:	n/a
30	chr6:110501372-110501422	ProgFib	skin:	n/a
31	chr6:110426718-110426768	CMK	blood:	n/a
32	chr6:110500691-110500741	U87	brain:	n/a
33	chr6:110501281-110501331	MCF10A-Er-Src	breast:	n/a
34	chr6:110426718-110426768	K562	blood:	n/a
35	chr6:110500390-110500440	HAEpiC	amniotic membrane:	n/a
36	chr6:110501370-110501420	PANC-1	pancreas:	n/a
37	chr6:110501370-110501420	ovcar-3	ovarian:	n/a
38	chr6:110500932-110500982	A549	lung:	n/a
39	chr6:110501627-110501677	U87	brain:	n/a
40	chr6:110501287-110501337	PrEC	prostate:	n/a
41	chr6:110501281-110501331	HMEC	breast:	n/a
42	chr6:110498910-110498960	NB4	blood:	n/a
43	chr6:110500990-110501040	HRE	kidney:	n/a
44	chr6:110500691-110500741	AG04450	lung:	fetal
45	chr6:110500390-110500440	HIPEpiC	eye:	n/a
46	chr6:110426718-110426768	AG09319	gingival:	n/a
47	chr6:110501077-110501127	HPAEpiC	pulmonary alveolar:	n/a
48	chr6:110500390-110500440	SK-N-MC	brain:	n/a
49	chr6:110501281-110501331	HEEpiC	esophagus:	n/a
50	chr6:110500337-110500387	Caco-2	colon:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:110499780..110500377-chr6:110663255..110663762,2	MCF-7	breast:
2	chr6:110495746..110497721-chr6:110499253..110502667,3	MCF-7	breast:
3	chr6:110474212..110476243-chr6:110478588..110481984,3	K562	blood:
4	chr6:110499873..110500385-chr6:110662588..110663229,2	MCF-7	breast:
5	chr6:110499927..110500847-chr6:110711777..110712638,2	MCF-7	breast:
6	chr6:110489268..110491516-chr6:110498726..110501361,2	K562	blood:
7	chr6:110474212..110476243-chr6:110478588..110481984,3	K562	blood:
8	chr6:110498361..110500396-chr6:110608264..110609928,2	K562	blood:
9	chr6:110499653..110501302-chr6:110501539..110503482,2	MCF-7	breast:
10	chr6:110499653..110501302-chr6:110501539..110503482,2	MCF-7	breast:
11	chr6:110496307..110499261-chr6:110709602..110711774,2	MCF-7	breast:
12	chr6:110501609..110503511-chr6:110521177..110523948,2	MCF-7	breast:
13	chr6:110423972..110426062-chr6:110431154..110433493,2	K562	blood:
14	chr6:110499478..110500346-chr6:110711664..110712335,3	MCF-7	breast:
15	chr6:110423972..110426062-chr6:110431154..110433493,2	K562	blood:
16	chr6:110494970..110497027-chr6:110498260..110500200,2	K562	blood:
17	chr6:110499550..110500398-chr6:110711587..110712606,4	K562	blood:
18	chr6:110481649..110484031-chr6:110507011..110509592,2	K562	blood:
19	chr6:110422372..110424640-chr6:110428766..110430402,2	K562	blood:
20	chr14:70193390..70193956-chr6:110499437..110500361,2	MCF-7	breast:
21	chr6:110494970..110497027-chr6:110498260..110500200,2	K562	blood:

No data

Variant related genes	Relation type
WASF1	TF binding region
CDC40	TF binding region
WASF1	CpG island
CDC40	CpG island
ENSG00000100650	chromatin interactions
ENSG00000112290	chromatin interactions
ENSG00000168438	chromatin interactions

Extended variants
information (count: 2756 )
Associated
traits (count: 113 )

Variant overlapped rSNPs/rCNVs (count:2756 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6940347	chr6:110426046-110426047	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs572239099	chr6:110426064-110426065	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs191812653	chr6:110426083-110426084	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs564452482	chr6:110426090-110426091	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs113824507	chr6:110426105-110426106	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs543449027	chr6:110426119-110426120	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs144961329	chr6:110426220-110426221	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs186274596	chr6:110426236-110426237	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs533329319	chr6:110426272-110426273	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs78984937	chr6:110426279-110426280	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs114252152	chr6:110426369-110426370	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs190742313	chr6:110426386-110426387	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs547670550	chr6:110426418-110426419	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs571127336	chr6:110426426-110426427	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs56304113	chr6:110426448-110426449	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs55638850	chr6:110426498-110426499	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs535894199	chr6:110426540-110426541	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs376406451	chr6:110426558-110426559	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs147560362	chr6:110426570-110426571	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs202138618	chr6:110426595-110426596	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs374884028	chr6:110426602-110426603	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs115861851	chr6:110426615-110426616	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs369277727	chr6:110426622-110426623	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs555868222	chr6:110426626-110426627	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs182246958	chr6:110426635-110426636	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs572442431	chr6:110426720-110426721	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs541224443	chr6:110426737-110426738	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs187753574	chr6:110426759-110426760	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs372562524	chr6:110426813-110426814	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs377218509	chr6:110426821-110426822	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs370423510	chr6:110426822-110426823	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs578010263	chr6:110426838-110426839	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs142009731	chr6:110426845-110426846	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs563554586	chr6:110426852-110426853	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs528931194	chr6:110426869-110426870	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs542249607	chr6:110426954-110426955	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs150102623	chr6:110426962-110426963	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs192755325	chr6:110426968-110426969	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs547982345	chr6:110427005-110427006	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs183195605	chr6:110427074-110427075	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs533469506	chr6:110427086-110427087	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs188535931	chr6:110427094-110427095	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs555496767	chr6:110427141-110427142	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs570002679	chr6:110427143-110427144	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs535887993	chr6:110427156-110427157	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs117801212	chr6:110427157-110427158	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs566174515	chr6:110427229-110427230	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs534774146	chr6:110427234-110427235	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs77986690	chr6:110427252-110427253	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs577941610	chr6:110427274-110427275	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:113)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Gastric cancer	17908304	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
Basal cell lymphoma	17170743	CNVD
Prostate cancer	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21785460	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Autism	17483303	CNVD
Chordoma	21602918	CNVD
Kartagener syndrome	16639409	CNVD
abnormal development	18461090	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Systemic lupus erythematosus	19220326	CNVD
Cancer	17160897	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Acute lymphoblastic leukemia	17229543	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Mental retardation	17621639	CNVD
Intellectual disability	22102821	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:1070 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:110417200-110438600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr6:110418200-110436000	Weak transcription	Fetal Brain Male	brain
3	chr6:110418800-110429000	Weak transcription	Fetal Muscle Leg	muscle
4	chr6:110418800-110437200	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr6:110419000-110426600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr6:110419000-110427400	Weak transcription	Fetal Lung	lung
7	chr6:110419000-110428000	Weak transcription	HSMM	muscle
8	chr6:110419000-110431800	Weak transcription	Rectal Smooth Muscle	rectum
9	chr6:110419000-110449600	Weak transcription	Brain Cingulate Gyrus	brain
10	chr6:110419000-110461800	Weak transcription	HSMMtube	muscle
11	chr6:110419200-110449600	Weak transcription	Brain Hippocampus Middle	brain
12	chr6:110419400-110430800	Weak transcription	Osteobl	bone
13	chr6:110419800-110429800	Strong transcription	Stomach Smooth Muscle	stomach
14	chr6:110419800-110436400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr6:110420000-110430000	Strong transcription	HUES64 Cell Line	embryonic stem cell
16	chr6:110420200-110427000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr6:110420400-110431200	Weak transcription	Fetal Heart	heart
18	chr6:110420600-110426400	Weak transcription	Left Ventricle	heart
19	chr6:110420600-110435200	Weak transcription	Brain Anterior Caudate	brain
20	chr6:110421200-110430200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr6:110421200-110433400	Weak transcription	K562	blood
22	chr6:110421400-110430000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr6:110422400-110426200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
24	chr6:110422800-110428200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr6:110423000-110426400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr6:110423200-110427400	Weak transcription	HUES6 Cell Line	embryonic stem cell
27	chr6:110423200-110427400	Weak transcription	Gastric	stomach
28	chr6:110423200-110429600	Weak transcription	NH-A	brain
29	chr6:110423200-110440800	Weak transcription	Cortex derived primary cultured neurospheres	brain
30	chr6:110423200-110448400	Weak transcription	Muscle Satellite Cultured Cells	--
31	chr6:110423400-110426200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr6:110423400-110426200	Weak transcription	NHLF	lung
33	chr6:110423400-110426600	Weak transcription	Pancreas	Pancrea
34	chr6:110423400-110427800	Weak transcription	HepG2	liver
35	chr6:110423400-110431400	Weak transcription	Fetal Thymus	thymus
36	chr6:110423400-110434000	Weak transcription	HMEC	breast
37	chr6:110423400-110437600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr6:110423400-110439000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr6:110423400-110445000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr6:110423400-110450000	Weak transcription	H9 Cell Line	embryonic stem cell
41	chr6:110423400-110459000	Weak transcription	Fetal Stomach	stomach
42	chr6:110423400-110459200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr6:110423400-110459200	Weak transcription	Aorta	Aorta
44	chr6:110423600-110427800	Weak transcription	Primary B cells from peripheral blood	blood
45	chr6:110423800-110426800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
46	chr6:110423800-110427000	Weak transcription	Primary B cells from cord blood	blood
47	chr6:110424000-110426200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr6:110424000-110427400	Weak transcription	Fetal Brain Female	brain
49	chr6:110424000-110427600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr6:110424200-110427800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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