Variant report

Variant	nsv830779
Chromosome Location	chr6:114206534-114246099
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	chr6:114243642-114243715	K562	blood:	n/a	n/a
2	ARID3A	chr6:114241762-114242855	K562	blood:	n/a	n/a
3	ARID3A	chr6:114230465-114230844	K562	blood:	n/a	n/a
4	ARID3A	chr6:114230480-114230810	HepG2	liver:	n/a	n/a
5	ATF1	chr6:114242063-114242745	K562	blood:	n/a	n/a
6	ATF1	chr6:114216476-114216695	K562	blood:	n/a	n/a
7	BACH1	chr6:114215139-114215228	H1-hESC	embryonic stem cell:	n/a	n/a
8	BHLHE40	chr6:114225041-114225347	HepG2	liver:	n/a	n/a
9	BHLHE40	chr6:114241848-114242439	K562	blood:	n/a	n/a
10	CBX3	chr6:114241920-114242748	K562	blood:	n/a	n/a
11	CBX3	chr6:114242018-114242419	K562	blood:	n/a	n/a
12	CCNT2	chr6:114242078-114242418	K562	blood:	n/a	n/a
13	CEBPB	chr6:114241566-114242662	K562	blood:	n/a	n/a
14	CEBPB	chr6:114242065-114242444	K562	blood:	n/a	n/a
15	CEBPB	chr6:114216507-114216784	K562	blood:	n/a	n/a
16	CEBPB	chr6:114216036-114216755	IMR90	lung:	n/a	chr6:114216164-114216175
17	CEBPB	chr6:114216550-114216688	A549	lung:	n/a	n/a
18	CEBPB	chr6:114239792-114240072	K562	blood:	n/a	n/a
19	CEBPD	chr6:114241979-114242477	K562	blood:	n/a	n/a
20	CEBPD	chr6:114241970-114242777	K562	blood:	n/a	n/a
21	CTCF	chr6:114230500-114230650	HUVEC	blood vessel:	n/a	chr6:114230618-114230626 chr6:114230615-114230628 chr6:114230613-114230631 chr6:114230608-114230629 chr6:114230614-114230630
22	CTCF	chr6:114228320-114228470	NHDF-neo	bronchial:	n/a	n/a
23	CTCF	chr6:114230382-114230831	IMR90	lung:	n/a	chr6:114230618-114230626 chr6:114230615-114230628 chr6:114230613-114230631 chr6:114230608-114230629 chr6:114230614-114230630
24	CTCF	chr6:114230513-114230738	LNCaP	prostate:	n/a	chr6:114230618-114230626 chr6:114230615-114230628 chr6:114230613-114230631 chr6:114230608-114230629 chr6:114230614-114230630
25	CTCF	chr6:114246060-114246210	AG10803	skin:	n/a	n/a
26	CTCF	chr6:114230500-114230650	RPTEC	kidney:	n/a	chr6:114230618-114230626 chr6:114230615-114230628 chr6:114230613-114230631 chr6:114230608-114230629 chr6:114230614-114230630
27	CTCF	chr6:114228380-114228530	GM12878	blood:	n/a	n/a
28	CTCF	chr6:114230520-114230670	BJ	skin:	n/a	chr6:114230618-114230626 chr6:114230615-114230628 chr6:114230613-114230631 chr6:114230608-114230629 chr6:114230614-114230630
29	CTCF	chr6:114228320-114228470	GM06990	blood:	n/a	n/a
30	CTCF	chr6:114228399-114228549	HepG2	liver:	n/a	n/a
31	CTCF	chr6:114230560-114230710	HL-60	blood:	n/a	chr6:114230618-114230626 chr6:114230615-114230628 chr6:114230613-114230631 chr6:114230608-114230629 chr6:114230614-114230630
32	CTCF	chr6:114230388-114230806	MCF-7	breast:	n/a	chr6:114230618-114230626 chr6:114230615-114230628 chr6:114230613-114230631 chr6:114230608-114230629 chr6:114230614-114230630
33	CTCF	chr6:114230513-114230759	GM13977	blood:	n/a	chr6:114230618-114230626 chr6:114230615-114230628 chr6:114230613-114230631 chr6:114230608-114230629 chr6:114230614-114230630
34	CTCF	chr6:114230500-114230650	WI-38	lung:	n/a	chr6:114230618-114230626 chr6:114230615-114230628 chr6:114230613-114230631 chr6:114230608-114230629 chr6:114230614-114230630
35	CTCF	chr6:114230400-114230550	WI-38	lung:	n/a	n/a
36	CTCF	chr6:114228420-114228570	HCPEpiC	choroid plexus:	n/a	n/a
37	CTCF	chr6:114230969-114230997	GM13977	blood:	n/a	n/a
38	CTCF	chr6:114230520-114230670	BE2_C	brain:	n/a	chr6:114230618-114230626 chr6:114230615-114230628 chr6:114230613-114230631 chr6:114230608-114230629 chr6:114230614-114230630
39	CTCF	chr6:114228460-114228610	SK-N-SH_RA	brain:	n/a	n/a
40	CTCF	chr6:114230540-114230690	GM12868	blood:	n/a	chr6:114230618-114230626 chr6:114230615-114230628 chr6:114230613-114230631 chr6:114230608-114230629 chr6:114230614-114230630
41	CTCF	chr6:114230560-114230710	SK-N-SH_RA	brain:	n/a	chr6:114230618-114230626 chr6:114230615-114230628 chr6:114230613-114230631 chr6:114230608-114230629 chr6:114230614-114230630
42	CTCF	chr6:114228400-114228550	HCPEpiC	choroid plexus:	n/a	n/a
43	CTCF	chr6:114230560-114230710	AG04449	skin:	n/a	chr6:114230618-114230626 chr6:114230615-114230628 chr6:114230613-114230631 chr6:114230608-114230629 chr6:114230614-114230630
44	CTCF	chr6:114230500-114230650	K562	blood:	n/a	chr6:114230618-114230626 chr6:114230615-114230628 chr6:114230613-114230631 chr6:114230608-114230629 chr6:114230614-114230630
45	CTCF	chr6:114228428-114228580	HUVEC	blood vessel:	n/a	n/a
46	CTCF	chr6:114228200-114228490	GM12865	blood:	n/a	n/a
47	CTCF	chr6:114230520-114230670	HAc	cerebellar:	n/a	chr6:114230618-114230626 chr6:114230615-114230628 chr6:114230613-114230631 chr6:114230608-114230629 chr6:114230614-114230630
48	CTCF	chr6:114230540-114230690	GM12875	blood:	n/a	chr6:114230618-114230626 chr6:114230615-114230628 chr6:114230613-114230631 chr6:114230608-114230629 chr6:114230614-114230630
49	CTCF	chr6:114230500-114230650	GM12875	blood:	n/a	chr6:114230618-114230626 chr6:114230615-114230628 chr6:114230613-114230631 chr6:114230608-114230629 chr6:114230614-114230630
50	CTCF	chr6:114228380-114228530	AG04450	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:114225012-114225062	AG04449	skin:	fetal
2	chr6:114225023-114225073	ovcar-3	ovarian:	n/a
3	chr6:114215021-114215071	HRE	kidney:	n/a
4	chr6:114225306-114225356	GM06990	blood:	n/a
5	chr6:114225023-114225073	H1-hESC	embryonic stem cell:	embryo
6	chr6:114225023-114225073	A549	lung:	n/a
7	chr6:114225023-114225073	HEEpiC	esophagus:	n/a
8	chr6:114225012-114225062	HMEC	breast:	n/a
9	chr6:114215021-114215071	K562	blood:	n/a
10	chr6:114225306-114225356	PANC-1	pancreas:	n/a
11	chr6:114225023-114225073	AG09309	skin:	n/a
12	chr6:114225012-114225062	GM06990	blood:	n/a
13	chr6:114215021-114215071	AoSMC	blood vessel:	n/a
14	chr6:114215021-114215071	SK-N-MC	brain:	n/a
15	chr6:114225012-114225062	K562	blood:	n/a
16	chr6:114225306-114225356	AG10803	skin:	n/a
17	chr6:114225012-114225062	HCM	heart:	n/a
18	chr6:114215021-114215071	NH-A	brain:	n/a
19	chr6:114225023-114225073	PrEC	prostate:	n/a
20	chr6:114225306-114225356	AG04450	lung:	fetal
21	chr6:114225306-114225356	U87	brain:	n/a
22	chr6:114225306-114225356	RPTEC	kidney:	n/a
23	chr6:114225023-114225073	U87	brain:	n/a
24	chr6:114215021-114215071	T-47D	breast:	n/a
25	chr6:114225306-114225356	HCT-116	colon:	n/a
26	chr6:114225306-114225356	GM19239	blood:	n/a
27	chr6:114215021-114215071	SAEC	small airway:	n/a
28	chr6:114225306-114225356	ovcar-3	ovarian:	n/a
29	chr6:114215021-114215071	NHBE	bronchial:	n/a
30	chr6:114225012-114225062	RPTEC	kidney:	n/a
31	chr6:114215021-114215071	HCM	heart:	n/a
32	chr6:114225012-114225062	PANC-1	pancreas:	n/a
33	chr6:114225306-114225356	H1-hESC	embryonic stem cell:	embryo
34	chr6:114225023-114225073	GM12892	blood:	n/a
35	chr6:114225306-114225356	HRPEpiC	eye:	n/a
36	chr6:114215021-114215071	GM12891	blood:	n/a
37	chr6:114225012-114225062	MCF10A-Er-Src	breast:	n/a
38	chr6:114225012-114225062	AoSMC	blood vessel:	n/a
39	chr6:114215021-114215071	HRCEpiC	kidney:	n/a
40	chr6:114225012-114225062	HRCEpiC	kidney:	n/a
41	chr6:114225306-114225356	GM12878	blood:	n/a
42	chr6:114225023-114225073	T-47D	breast:	n/a
43	chr6:114225012-114225062	GM12892	blood:	n/a
44	chr6:114215021-114215071	Caco-2	colon:	n/a
45	chr6:114215021-114215071	RPTEC	kidney:	n/a
46	chr6:114225012-114225062	HNPCEpiC	eye:	n/a
47	chr6:114225306-114225356	LNCaP	prostate:	n/a
48	chr6:114225306-114225356	IMR90	lung:	fetal
49	chr6:114215021-114215071	LNCaP	prostate:	n/a
50	chr6:114225306-114225356	HPAEpiC	pulmonary alveolar:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:114213735..114217025-chr6:114218822..114221280,4	K562	blood:
2	chr6:114209973..114211812-chr6:114213161..114214675,2	K562	blood:
3	chr6:114239524..114241632-chr6:114242865..114244629,2	MCF-7	breast:
4	chr6:114245318..114247054-chr6:114255867..114258727,3	K562	blood:
5	chr6:114226817..114229049-chr6:114230509..114233303,2	K562	blood:
6	chr6:114179382..114181466-chr6:114226891..114229002,2	MCF-7	breast:
7	chr6:114234076..114236200-chr6:114237531..114240425,2	K562	blood:
8	chr6:114203918..114205752-chr6:114209292..114211804,3	K562	blood:
9	chr6:114234076..114236200-chr6:114237531..114240425,2	K562	blood:
10	chr6:114241819..114244769-chr6:114245908..114248652,2	K562	blood:
11	chr6:114209899..114211985-chr6:114212555..114214412,2	MCF-7	breast:
12	chr6:114218743..114220678-chr6:114223116..114225137,2	MCF-7	breast:
13	chr6:114183529..114185723-chr6:114208542..114210250,2	MCF-7	breast:
14	chr6:114239524..114241632-chr6:114242865..114244629,2	MCF-7	breast:
15	chr6:114200223..114202562-chr6:114240736..114243361,2	K562	blood:
16	chr6:114209973..114211812-chr6:114213161..114214675,2	K562	blood:
17	chr6:114226817..114229049-chr6:114230509..114233303,2	K562	blood:
18	chr6:114241819..114244769-chr6:114245908..114248652,2	K562	blood:
19	chr6:114213735..114217025-chr6:114218822..114221280,4	K562	blood:
20	chr6:114201759..114204055-chr6:114207558..114209101,2	MCF-7	breast:
21	chr6:114218743..114220678-chr6:114223116..114225137,2	MCF-7	breast:
22	chr6:114245404..114247050-chr6:114257161..114258727,2	K562	blood:
23	chr6:114209899..114211985-chr6:114212555..114214412,2	MCF-7	breast:
24	chr6:114225067..114227184-chr6:114227873..114230239,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MARCKS-1	chr6:114238107-114238216	ENSG00000175967.3
2	lnc-MARCKS-1	chr6:114241620-114241826	XLOC_005438
3	lnc-MARCKS-1	chr6:114225551-114225908	XLOC_005438
4	lnc-MARCKS-1	chr6:114240271-114240621	ENSG00000175967.3
5	lnc-MARCKS-1	chr6:114241620-114242806	ENSG00000175967.3
6	lnc-MARCKS-1	chr6:114240271-114240621	XLOC_005438
7	lnc-MARCKS-1	chr6:114240762-114240795	XLOC_005438
8	lnc-MARCKS-1	chr6:114225302-114225908	ENSG00000175967.3
9	lnc-MARCKS-8	chr6:114219725-114220039	NONHSAT114576
10	lnc-MARCKS-1	chr6:114238107-114238216	XLOC_005438
11	lnc-MARCKS-1	chr6:114241620-114242806	XLOC_005438

Variant related genes	Relation type
ENSG00000175967	TF binding region
ENSG00000175967	CpG island
ENSG00000175967	chromatin interactions
SPTLC1	miRNA target sites
SPTBN2	miRNA target sites

Extended variants
information (count: 1619 )
Associated
traits (count: 117 )

Variant overlapped rSNPs/rCNVs (count:1619 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs559220833	chr6:114206546-114206547	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs80209802	chr6:114206572-114206573	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs182752343	chr6:114206591-114206592	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs76084664	chr6:114206597-114206598	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs75769488	chr6:114206609-114206610	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs76884870	chr6:114206621-114206622	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs145119113	chr6:114206623-114206624	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs115148176	chr6:114206648-114206649	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs115690474	chr6:114206658-114206659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs116130636	chr6:114206659-114206660	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs73768571	chr6:114206686-114206687	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs187308544	chr6:114206705-114206706	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs80342661	chr6:114206719-114206720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs73768572	chr6:114206743-114206744	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs191789505	chr6:114206783-114206784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs538349375	chr6:114206785-114206786	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs78495111	chr6:114206791-114206792	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs371958101	chr6:114206795-114206796	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs531529062	chr6:114206798-114206799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs75032069	chr6:114206806-114206807	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs35949515	chr6:114206830-114206831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs114379620	chr6:114206837-114206838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs114943650	chr6:114206839-114206840	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs116004073	chr6:114206887-114206888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs116224746	chr6:114206889-114206890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs146840001	chr6:114206906-114206907	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs532071507	chr6:114206914-114206915	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs200836545	chr6:114206923-114206924	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs74414492	chr6:114206931-114206932	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs575699526	chr6:114206933-114206934	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs547475219	chr6:114207016-114207017	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs184867939	chr6:114207048-114207049	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs529686001	chr6:114207050-114207051	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs12213840	chr6:114207062-114207063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs140096055	chr6:114207158-114207159	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs150286355	chr6:114207162-114207163	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs667525	chr6:114207181-114207182	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs552766785	chr6:114207199-114207200	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs115562512	chr6:114207212-114207213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs138035230	chr6:114207242-114207243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs143501998	chr6:114207244-114207245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs116830957	chr6:114207260-114207261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs534760545	chr6:114207280-114207281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs187732477	chr6:114207300-114207301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs542640082	chr6:114207304-114207305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs554543359	chr6:114207307-114207308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs553427504	chr6:114207309-114207310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs574871805	chr6:114207341-114207342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs535820819	chr6:114207348-114207349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs576304467	chr6:114207352-114207353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:117)

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
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
Breast cancer	21364760	CNVD
Chordoma	21602918	CNVD
Kartagener syndrome	16639409	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
Hypoplastic	20877625	CNVD
Hypotonia	20877625	CNVD
Mental retardation	20877625	CNVD
Microcephaly	20877625	CNVD
brachycephaly	20877625	CNVD
epicanthic folds	20877625	CNVD
micrognathia	20877625	CNVD
small cell lung cancer	20016488	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:280 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:114203800-114208800	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr6:114205800-114210600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr6:114206200-114209800	Weak transcription	Fetal Muscle Leg	muscle
4	chr6:114206400-114207200	Enhancers	Adipose Nuclei	Adipose
5	chr6:114208800-114209800	Enhancers	Rectal Mucosa Donor 31	rectum
6	chr6:114209400-114209600	Enhancers	Small Intestine	intestine
7	chr6:114209600-114210800	Enhancers	NHDF-Ad	bronchial
8	chr6:114209800-114210200	Enhancers	Fetal Muscle Leg	muscle
9	chr6:114210400-114210800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr6:114210800-114214600	Weak transcription	NHDF-Ad	bronchial
11	chr6:114214000-114215200	Enhancers	Primary neutrophils fromperipheralblood	blood
12	chr6:114214200-114216400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr6:114214600-114215000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr6:114214600-114215800	Enhancers	NHDF-Ad	bronchial
15	chr6:114214600-114216400	Enhancers	Osteobl	bone
16	chr6:114214800-114215200	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr6:114214800-114215800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr6:114214800-114215800	Enhancers	HUVEC	blood vessel
19	chr6:114215000-114215400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr6:114215000-114215800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr6:114215000-114216400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr6:114215400-114222800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr6:114215600-114216400	Enhancers	Fetal Stomach	stomach
24	chr6:114215800-114216000	Weak transcription	NHDF-Ad	bronchial
25	chr6:114215800-114217000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr6:114216000-114217400	Enhancers	Primary hematopoietic stem cells short term culture	blood
27	chr6:114216200-114217200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr6:114216200-114218000	Enhancers	Colon Smooth Muscle	Colon
29	chr6:114216400-114216600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr6:114216800-114217800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr6:114217000-114217800	Enhancers	H1 Cell Line	embryonic stem cell
32	chr6:114217600-114218000	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr6:114218000-114223200	Weak transcription	Colon Smooth Muscle	Colon
34	chr6:114222200-114222400	Enhancers	Sigmoid Colon	Sigmoid Colon
35	chr6:114222200-114223600	Enhancers	Rectal Mucosa Donor 31	rectum
36	chr6:114222400-114223000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr6:114222400-114223000	Weak transcription	Sigmoid Colon	Sigmoid Colon
38	chr6:114222400-114223200	Weak transcription	NHDF-Ad	bronchial
39	chr6:114222600-114223400	Enhancers	Muscle Satellite Cultured Cells	--
40	chr6:114222600-114223600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr6:114222800-114223000	Enhancers	HUVEC	blood vessel
42	chr6:114222800-114224000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr6:114222800-114224000	Enhancers	Fetal Muscle Leg	muscle
44	chr6:114223000-114223400	Enhancers	Osteobl	bone
45	chr6:114223000-114223600	Enhancers	Sigmoid Colon	Sigmoid Colon
46	chr6:114223000-114225200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr6:114223000-114225200	Weak transcription	HUVEC	blood vessel
48	chr6:114223200-114223400	Enhancers	Fetal Muscle Trunk	muscle
49	chr6:114223200-114223400	Enhancers	NHDF-Ad	bronchial
50	chr6:114223200-114223600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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