Variant report

Variant	nsv515895
Chromosome Location	chr6:100868779-100910798
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	BACH1	chr6:100909343-100909496	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr6:100903060-100903315	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr6:100905663-100906313	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr6:100909923-100910152	GM12878	blood:	n/a	n/a
5	BRCA1	chr6:100903542-100903770	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr6:100878859-100879189	K562	blood:	n/a	chr6:100879030-100879043 chr6:100879031-100879042 chr6:100879030-100879043
7	CEBPB	chr6:100875332-100875661	MCF-7	breast:	n/a	chr6:100875465-100875476 chr6:100875465-100875478 chr6:100875515-100875524 chr6:100875513-100875524
8	CEBPB	chr6:100878855-100879089	HepG2	liver:	n/a	chr6:100879030-100879043 chr6:100879031-100879042 chr6:100879030-100879043
9	CEBPB	chr6:100875334-100875699	K562	blood:	n/a	chr6:100875465-100875476 chr6:100875465-100875478 chr6:100875515-100875524 chr6:100875513-100875524
10	CEBPB	chr6:100875331-100875689	Hela-S3	cervix:	n/a	chr6:100875465-100875476 chr6:100875465-100875478 chr6:100875515-100875524 chr6:100875513-100875524
11	CEBPB	chr6:100875372-100875715	ECC-1	luminal epithelium:	n/a	chr6:100875465-100875476 chr6:100875465-100875478 chr6:100875515-100875524 chr6:100875513-100875524
12	CEBPB	chr6:100894518-100894546	K562	blood:	n/a	n/a
13	CEBPB	chr6:100894399-100894676	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr6:100878936-100879193	A549	lung:	n/a	chr6:100879030-100879043 chr6:100879031-100879042 chr6:100879030-100879043
15	CEBPB	chr6:100875344-100875686	IMR90	lung:	n/a	chr6:100875465-100875476 chr6:100875465-100875478 chr6:100875515-100875524 chr6:100875513-100875524
16	CHD1	chr6:100909301-100909445	H1-hESC	embryonic stem cell:	n/a	chr6:100909337-100909347
17	CHD2	chr6:100902135-100902411	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr6:100903487-100904147	H1-hESC	embryonic stem cell:	n/a	n/a
19	CREB1	chr6:100895715-100896376	H1-hESC	embryonic stem cell:	n/a	n/a
20	CREB1	chr6:100895830-100896337	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTBP2	chr6:100905106-100907142	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTBP2	chr6:100903148-100904421	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTBP2	chr6:100908904-100909528	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr6:100903300-100903450	BJ	skin:	n/a	n/a
25	CTCF	chr6:100908560-100908710	SK-N-SH_RA	brain:	n/a	chr6:100908615-100908633
26	CTCF	chr6:100908438-100908695	A549	lung:	n/a	chr6:100908615-100908633
27	CTCF	chr6:100908520-100908670	HMF	breast:	n/a	chr6:100908615-100908633
28	CTCF	chr6:100909512-100909529	Medullo	brain:	n/a	n/a
29	CTCF	chr6:100908640-100908790	HEEpiC	esophagus:	n/a	n/a
30	CTCF	chr6:100908580-100908730	HVMF	connective:	n/a	chr6:100908615-100908633
31	CTCF	chr6:100908960-100909110	AG10803	skin:	n/a	n/a
32	CTCF	chr6:100883640-100883790	Caco-2	colon:	n/a	n/a
33	CTCF	chr6:100894480-100894630	BJ	skin:	n/a	chr6:100894512-100894530 chr6:100894512-100894525 chr6:100894515-100894528
34	CTCF	chr6:100894420-100894570	HRE	kidney:	n/a	chr6:100894512-100894530 chr6:100894512-100894525 chr6:100894515-100894528
35	CTCF	chr6:100908700-100908850	GM12871	blood:	n/a	n/a
36	CTCF	chr6:100908540-100908690	K562	blood:	n/a	chr6:100908615-100908633
37	CTCF	chr6:100908520-100908670	HepG2	liver:	n/a	chr6:100908615-100908633
38	CTCF	chr6:100908520-100908670	Hela-S3	cervix:	n/a	chr6:100908615-100908633
39	CTCF	chr6:100908540-100908690	HL-60	blood:	n/a	chr6:100908615-100908633
40	CTCF	chr6:100894420-100894570	GM06990	blood:	n/a	chr6:100894512-100894530 chr6:100894512-100894525 chr6:100894515-100894528
41	CTCF	chr6:100894460-100894610	HRE	kidney:	n/a	chr6:100894512-100894530 chr6:100894512-100894525 chr6:100894515-100894528
42	CTCF	chr6:100908544-100908668	HepG2	liver:	n/a	chr6:100908615-100908633
43	CTCF	chr6:100894480-100894630	HEEpiC	esophagus:	n/a	chr6:100894512-100894530 chr6:100894512-100894525 chr6:100894515-100894528
44	CTCF	chr6:100908520-100908670	HEK293	kidney:	n/a	chr6:100908615-100908633
45	CTCF	chr6:100908580-100908730	GM12878	blood:	n/a	chr6:100908615-100908633
46	CTCF	chr6:100908480-100908630	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr6:100908519-100908739	Kidney_OC	kidney:	n/a	chr6:100908615-100908633
48	CTCF	chr6:100908500-100908650	GM12878	blood:	n/a	chr6:100908615-100908633
49	CTCF	chr6:100908541-100908655	GM19238	blood:	n/a	chr6:100908615-100908633
50	CTCF	chr6:100908480-100908630	SAEC	small airway:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:100906685-100906735	GM19239	blood:	n/a
2	chr6:100896760-100896810	Caco-2	colon:	n/a
3	chr6:100874816-100874866	HMEC	breast:	n/a
4	chr6:100905587-100905637	ProgFib	skin:	n/a
5	chr6:100904055-100904105	A549	lung:	n/a
6	chr6:100898784-100898834	NB4	blood:	n/a
7	chr6:100906685-100906735	GM19239	blood:	n/a
8	chr6:100896760-100896810	Caco-2	colon:	n/a
9	chr6:100874816-100874866	HMEC	breast:	n/a
10	chr6:100905587-100905637	ProgFib	skin:	n/a
11	chr6:100904055-100904105	A549	lung:	n/a
12	chr6:100898784-100898834	NB4	blood:	n/a
13	chr6:100903227-100903277	GM12892	blood:	n/a
14	chr6:100903691-100903741	GM19239	blood:	n/a
15	chr6:100902470-100902520	SK-N-SH_RA	brain:	n/a
16	chr6:100895907-100895957	NHDF-neo	bronchial:	n/a
17	chr6:100906182-100906232	HPAEpiC	pulmonary alveolar:	n/a
18	chr6:100906182-100906232	A549	lung:	n/a
19	chr6:100893665-100893715	HRCEpiC	kidney:	n/a
20	chr6:100902093-100902143	NB4	blood:	n/a
21	chr6:100896392-100896442	HEEpiC	esophagus:	n/a
22	chr6:100903691-100903741	ovcar-3	ovarian:	n/a
23	chr6:100895143-100895193	GM12891	blood:	n/a
24	chr6:100903691-100903741	SK-N-SH	brain:	n/a
25	chr6:100894629-100894679	AG09309	skin:	n/a
26	chr6:100901804-100901854	GM12891	blood:	n/a
27	chr6:100895050-100895100	H1-hESC	embryonic stem cell:	embryo
28	chr6:100904055-100904105	ovcar-3	ovarian:	n/a
29	chr6:100895481-100895531	NH-A	brain:	n/a
30	chr6:100895211-100895261	LNCaP	prostate:	n/a
31	chr6:100896803-100896853	ECC-1	luminal epithelium:	n/a
32	chr6:100891601-100891651	SK-N-SH_RA	brain:	n/a
33	chr6:100895618-100895668	HIPEpiC	eye:	n/a
34	chr6:100882035-100882085	SAEC	small airway:	n/a
35	chr6:100895143-100895193	BJ	skin:	n/a
36	chr6:100903227-100903277	NHDF-neo	bronchial:	n/a
37	chr6:100893665-100893715	GM12891	blood:	n/a
38	chr6:100903817-100903867	Hepatocyte	liver:	n/a
39	chr6:100901804-100901854	IMR90	lung:	fetal
40	chr6:100909443-100909493	ovcar-3	ovarian:	n/a
41	chr6:100903575-100903625	AG10803	skin:	n/a
42	chr6:100901371-100901421	ECC-1	luminal epithelium:	n/a
43	chr6:100903909-100903959	HPAEpiC	pulmonary alveolar:	n/a
44	chr6:100896760-100896810	HCT-116	colon:	n/a
45	chr6:100903909-100903959	HCM	heart:	n/a
46	chr6:100894629-100894679	Jurkat	blood:	n/a
47	chr6:100897309-100897359	SK-N-MC	brain:	n/a
48	chr6:100909121-100909171	U87	brain:	n/a
49	chr6:100905691-100905741	AG04449	skin:	fetal
50	chr6:100898784-100898834	ECC-1	luminal epithelium:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:100895834..100897830-chr6:100900625..100903178,2	K562	blood:
2	chr6:100894013..100895525-chr6:100899314..100902220,2	MCF-7	breast:
3	chr6:100885282..100888001-chr6:100892746..100894898,2	K562	blood:
4	chr6:100887121..100888891-chr6:100901432..100903601,2	MCF-7	breast:
5	chr6:100906855..100909524-chr6:100935004..100937170,2	MCF-7	breast:
6	chr6:100895834..100897830-chr6:100900574..100903178,3	K562	blood:
7	chr6:100887121..100888891-chr6:100901432..100903601,2	MCF-7	breast:
8	chr6:100908327..100910621-chr6:100914553..100916127,2	MCF-7	breast:
9	chr6:100907831..100909801-chr6:100918117..100920075,2	MCF-7	breast:
10	chr6:100883478..100885403-chr6:100886324..100888180,2	K562	blood:
11	chr6:100887185..100889268-chr6:100914294..100916955,2	MCF-7	breast:
12	chr6:100869406..100871718-chr6:100874108..100875813,2	MCF-7	breast:
13	chr6:100876201..100879163-chr6:100881481..100884143,2	K562	blood:
14	chr6:100867794..100869514-chr6:100873709..100875237,2	K562	blood:
15	chr6:100876201..100879163-chr6:100881481..100884143,2	K562	blood:
16	chr4:122383570..122384412-chr6:100888804..100889304,2	MCF-7	breast:
17	chr6:100883478..100885403-chr6:100886324..100888180,2	K562	blood:
18	chr6:100895834..100897830-chr6:100900574..100903178,3	K562	blood:
19	chr6:100895834..100897830-chr6:100900625..100903178,2	K562	blood:
20	chr6:100894013..100895525-chr6:100899314..100902220,2	MCF-7	breast:
21	chr6:100854348..100856456-chr6:100877921..100879422,2	MCF-7	breast:
22	chr6:100885282..100888001-chr6:100892746..100894898,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRDM13-4	chr6:100885132-100885360	ENSG00000228082.1
2	lnc-PRDM13-4	chr6:100874994-100875144	ENSG00000228082.1

Variant related genes	Relation type
ENSG00000228082	TF binding region
ENSG00000228082	CpG island
ENSG00000228082	chromatin interactions

Extended variants
information (count: 1458 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:1458 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3734354	chr6:100868779-100868780	Enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs201750202	chr6:100868809-100868810	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs188177953	chr6:100868847-100868848	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs148377236	chr6:100868891-100868892	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs373616976	chr6:100868951-100868952	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs199503910	chr6:100868983-100868984	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs574385630	chr6:100869015-100869016	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs541659941	chr6:100869041-100869042	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs560261457	chr6:100869042-100869043	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs367716435	chr6:100869102-100869103	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs545837074	chr6:100869133-100869134	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs563936139	chr6:100869203-100869204	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs565245432	chr6:100869218-100869219	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs180801099	chr6:100869303-100869304	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs117244754	chr6:100869339-100869340	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs562395693	chr6:100869350-100869351	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs529595471	chr6:100869351-100869352	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs547688502	chr6:100869423-100869424	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs141392811	chr6:100869556-100869557	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs78207282	chr6:100869598-100869599	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs551809573	chr6:100869621-100869622	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs543825918	chr6:100869658-100869659	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs35291121	chr6:100869673-100869674	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs150828729	chr6:100869694-100869695	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs529831163	chr6:100869755-100869756	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs574410536	chr6:100869826-100869827	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs76739148	chr6:100869835-100869836	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs66538288	chr6:100869849-100869850	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs59503250	chr6:100869882-100869883	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs397960957	chr6:100869886-100869887	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs572166160	chr6:100869900-100869901	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs545671885	chr6:100869949-100869950	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs78547050	chr6:100870048-100870049	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs564216521	chr6:100870086-100870087	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs532218030	chr6:100870096-100870097	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs145994395	chr6:100870113-100870114	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs561634189	chr6:100870182-100870183	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs552356120	chr6:100870204-100870205	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs117686740	chr6:100870205-100870206	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs538106301	chr6:100870227-100870228	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs548021553	chr6:100870264-100870265	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs139939279	chr6:100870266-100870267	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs183890205	chr6:100870292-100870293	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs551676638	chr6:100870344-100870345	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs569840679	chr6:100870375-100870376	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs149744120	chr6:100870451-100870452	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs567533975	chr6:100870462-100870463	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs190371303	chr6:100870504-100870505	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs72937677	chr6:100870537-100870538	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs182559046	chr6:100870551-100870552	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:104)

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
Endometrioid adenocarcinoma	16974079	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
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	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
Prostate cancer	17245344	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Cancer	20164920	CNVD
Burkitt''s lymphoma	20823134	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	17640729	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
small cell lung cancer	20016488	CNVD
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17170743	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21785460	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Myelofibrosis	22110671	CNVD
Obesity	21045960	CNVD
Liver carcinoma	19366792	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD

Chromatin state (count:877 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:100831200-100874000	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr6:100838400-100874800	Weak transcription	Psoas Muscle	Psoas
3	chr6:100839400-100874200	Weak transcription	HSMM	muscle
4	chr6:100852200-100871200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr6:100856800-100874800	Weak transcription	Fetal Muscle Leg	muscle
6	chr6:100862200-100890600	Weak transcription	Adipose Nuclei	Adipose
7	chr6:100863000-100894600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr6:100864000-100887000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr6:100864200-100870400	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr6:100864400-100869600	Weak transcription	Fetal Intestine Small	intestine
11	chr6:100865600-100869600	Weak transcription	Fetal Intestine Large	intestine
12	chr6:100867400-100889000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr6:100867600-100869000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr6:100867800-100868800	Enhancers	H9 Cell Line	embryonic stem cell
15	chr6:100867800-100869000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
16	chr6:100867800-100869000	Enhancers	H1 Cell Line	embryonic stem cell
17	chr6:100867800-100869400	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr6:100868000-100869200	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr6:100868000-100869200	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr6:100868000-100869400	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr6:100868000-100869600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr6:100868000-100869600	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr6:100868000-100869600	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr6:100868200-100868800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr6:100868200-100869600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr6:100868600-100868800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
27	chr6:100868800-100869000	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr6:100868800-100874200	Weak transcription	H9 Cell Line	embryonic stem cell
29	chr6:100869000-100869200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
30	chr6:100869000-100874000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr6:100869000-100874200	Weak transcription	H1 Cell Line	embryonic stem cell
32	chr6:100869000-100882200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
33	chr6:100869200-100869600	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr6:100869200-100873800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr6:100869200-100874600	Weak transcription	HUES64 Cell Line	embryonic stem cell
36	chr6:100869400-100874200	Weak transcription	HUES48 Cell Line	embryonic stem cell
37	chr6:100869400-100882200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr6:100869600-100870200	Enhancers	Fetal Intestine Large	intestine
39	chr6:100869600-100870400	Enhancers	Fetal Intestine Small	intestine
40	chr6:100869600-100874000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
41	chr6:100869600-100874200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr6:100869600-100874400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
43	chr6:100870400-100871600	Enhancers	Pancreatic Islets	Pancreatic Islet
44	chr6:100871200-100871400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr6:100871400-100871800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr6:100873600-100875600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr6:100873800-100874000	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr6:100874000-100874400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
49	chr6:100874000-100874400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr6:100874000-100874600	Enhancers	Muscle Satellite Cultured Cells	--

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