Variant report

Variant	nsv1022376
Chromosome Location	chr6:64386826-64445195
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:427)
CpG islands
(count:122)
Chromatin interactive
region (count:35)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:5)

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:64387165-64387637	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:64444667-64445117	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:64434630-64435248	HepG2	liver:	n/a	chr6:64434709-64434725
4	ARID3A	chr6:64418724-64419399	HepG2	liver:	n/a	n/a
5	ATF1	chr6:64387228-64387346	K562	blood:	n/a	n/a
6	ATF2	chr6:64392999-64393585	GM12878	blood:	n/a	n/a
7	BACH1	chr6:64405827-64405926	K562	blood:	n/a	n/a
8	BACH1	chr6:64415743-64415840	K562	blood:	n/a	n/a
9	BHLHE40	chr6:64393154-64393440	GM12878	blood:	n/a	n/a
10	BHLHE40	chr6:64444906-64445178	HepG2	liver:	n/a	n/a
11	BHLHE40	chr6:64387255-64387507	HepG2	liver:	n/a	n/a
12	BHLHE40	chr6:64395340-64395806	GM12878	blood:	n/a	n/a
13	CEBPB	chr6:64387238-64387610	K562	blood:	n/a	n/a
14	CEBPB	chr6:64387232-64387659	MCF-7	breast:	n/a	n/a
15	CEBPB	chr6:64419067-64419304	HepG2	liver:	n/a	n/a
16	CEBPB	chr6:64387236-64387618	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr6:64442319-64442768	Hela-S3	cervix:	n/a	chr6:64442570-64442578
18	CEBPB	chr6:64387310-64387525	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr6:64387303-64387599	HepG2	liver:	n/a	n/a
20	CEBPB	chr6:64387276-64387544	HepG2	liver:	n/a	n/a
21	CEBPB	chr6:64387213-64387616	MCF-7	breast:	n/a	n/a
22	CEBPB	chr6:64414357-64414395	IMR90	lung:	n/a	n/a
23	CEBPB	chr6:64387242-64387622	HepG2	liver:	n/a	n/a
24	CEBPB	chr6:64428784-64428943	IMR90	lung:	n/a	chr6:64428851-64428862
25	CEBPB	chr6:64387270-64387602	IMR90	lung:	n/a	n/a
26	CEBPB	chr6:64387210-64387555	HepG2	liver:	n/a	n/a
27	CEBPB	chr6:64428757-64429032	HepG2	liver:	n/a	chr6:64429014-64429026 chr6:64428851-64428862
28	CEBPB	chr6:64387300-64387616	A549	lung:	n/a	n/a
29	CEBPB	chr6:64387274-64387601	A549	lung:	n/a	n/a
30	CEBPB	chr6:64419031-64419394	HepG2	liver:	n/a	n/a
31	CEBPB	chr6:64387185-64387633	A549	lung:	n/a	n/a
32	CHD1	chr6:64393129-64393501	GM12878	blood:	n/a	n/a
33	CTCF	chr6:64399420-64399570	HCFaa	heart:	n/a	chr6:64399506-64399527
34	CTCF	chr6:64399400-64399550	AG09319	gingival:	n/a	chr6:64399506-64399527
35	CTCF	chr6:64399460-64399610	AG09319	gingival:	n/a	chr6:64399506-64399527
36	CTCF	chr6:64399520-64399670	HVMF	connective:	n/a	n/a
37	CTCF	chr6:64415960-64416110	GM12873	blood:	n/a	n/a
38	CTCF	chr6:64415405-64415501	Kidney_OC	kidney:	n/a	n/a
39	CTCF	chr6:64399420-64399570	AG04450	lung:	n/a	chr6:64399506-64399527
40	CTCF	chr6:64399320-64399470	HRE	kidney:	n/a	n/a
41	CTCF	chr6:64399440-64399590	HMF	breast:	n/a	chr6:64399506-64399527
42	CTCF	chr6:64399440-64399590	HCPEpiC	choroid plexus:	n/a	chr6:64399506-64399527
43	CTCF	chr6:64399460-64399610	HMF	breast:	n/a	chr6:64399506-64399527
44	CTCF	chr6:64435520-64435670	Caco-2	colon:	n/a	n/a
45	CTCF	chr6:64399482-64399572	HUVEC	blood vessel:	n/a	chr6:64399506-64399527
46	CTCF	chr6:64440780-64440858	GM10248	blood:	n/a	n/a
47	CTCF	chr6:64399500-64399650	BJ	skin:	n/a	chr6:64399506-64399527
48	CTCF	chr6:64399400-64399550	HPF	lung:	n/a	chr6:64399506-64399527
49	CTCF	chr6:64399380-64399530	Hela-S3	cervix:	n/a	chr6:64399506-64399527
50	CTCF	chr6:64399502-64399571	LNCaP	prostate:	n/a	chr6:64399506-64399527

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:64390047-64390097	HepG2	liver:	n/a
2	chr6:64423797-64423847	NHDF-neo	bronchial:	n/a
3	chr6:64423797-64423847	HCPEpiC	choroid plexus:	n/a
4	chr6:64423797-64423847	HEK293	kidney:	embryo
5	chr6:64390047-64390097	HCF	heart:	n/a
6	chr6:64390047-64390097	MCF-7	breast:	n/a
7	chr6:64390047-64390097	GM12878	blood:	n/a
8	chr6:64390047-64390097	HRCEpiC	kidney:	n/a
9	chr6:64423797-64423847	BJ	skin:	n/a
10	chr6:64390047-64390097	GM12891	blood:	n/a
11	chr6:64423797-64423847	MCF10A-Er-Src	breast:	n/a
12	chr6:64390047-64390097	NB4	blood:	n/a
13	chr6:64390047-64390097	ovcar-3	ovarian:	n/a
14	chr6:64423797-64423847	HMEC	breast:	n/a
15	chr6:64390047-64390097	BE2_C	brain:	n/a
16	chr6:64390047-64390097	SK-N-MC	brain:	n/a
17	chr6:64390047-64390097	HEEpiC	esophagus:	n/a
18	chr6:64390047-64390097	PFSK-1	brain:	n/a
19	chr6:64390047-64390097	K562	blood:	n/a
20	chr6:64423797-64423847	HCM	heart:	n/a
21	chr6:64423797-64423847	HCT-116	colon:	n/a
22	chr6:64423797-64423847	RPTEC	kidney:	n/a
23	chr6:64390047-64390097	HNPCEpiC	eye:	n/a
24	chr6:64423797-64423847	SK-N-SH_RA	brain:	n/a
25	chr6:64390047-64390097	HIPEpiC	eye:	n/a
26	chr6:64390047-64390097	PrEC	prostate:	n/a
27	chr6:64423797-64423847	AG04449	skin:	fetal
28	chr6:64390047-64390097	A549	lung:	n/a
29	chr6:64423797-64423847	ECC-1	luminal epithelium:	n/a
30	chr6:64390047-64390097	AG10803	skin:	n/a
31	chr6:64423797-64423847	HRPEpiC	eye:	n/a
32	chr6:64390047-64390097	U87	brain:	n/a
33	chr6:64423797-64423847	GM12891	blood:	n/a
34	chr6:64423797-64423847	HAEpiC	amniotic membrane:	n/a
35	chr6:64390047-64390097	Jurkat	blood:	n/a
36	chr6:64423797-64423847	Hela-S3	cervix:	n/a
37	chr6:64423797-64423847	HNPCEpiC	eye:	n/a
38	chr6:64390047-64390097	LNCaP	prostate:	n/a
39	chr6:64423797-64423847	SK-N-SH	brain:	n/a
40	chr6:64390047-64390097	HPAEpiC	pulmonary alveolar:	n/a
41	chr6:64423797-64423847	NH-A	brain:	n/a
42	chr6:64390047-64390097	HRPEpiC	eye:	n/a
43	chr6:64423797-64423847	NT2-D1	testis:	n/a
44	chr6:64423797-64423847	U87	brain:	n/a
45	chr6:64390047-64390097	SAEC	small airway:	n/a
46	chr6:64390047-64390097	H1-hESC	embryonic stem cell:	embryo
47	chr6:64423797-64423847	AoSMC	blood vessel:	n/a
48	chr6:64390047-64390097	Hepatocyte	liver:	n/a
49	chr6:64390047-64390097	IMR90	lung:	fetal
50	chr6:64390047-64390097	PANC-1	pancreas:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:64400258..64402209-chr6:64406199..64408000,2	K562	blood:
2	chr6:64386744..64388275-chr6:64400257..64402696,2	K562	blood:
3	chr6:64418755..64420387-chr6:64422922..64425376,2	K562	blood:
4	chr6:64420787..64422833-chr6:64423125..64427172,4	K562	blood:
5	chr6:64345547..64349156-chr6:64414533..64419389,4	K562	blood:
6	chr6:64282934..64284601-chr6:64393133..64394696,2	K562	blood:
7	chr6:64396895..64400297-chr6:64403674..64407120,4	K562	blood:
8	chr6:64347461..64349165-chr6:64396342..64398673,2	K562	blood:
9	chr6:64386744..64388275-chr6:64400257..64402696,2	K562	blood:
10	chr6:64420787..64422833-chr6:64423125..64427172,4	K562	blood:
11	chr6:64427838..64430410-chr6:64430505..64432521,2	K562	blood:
12	chr6:64396895..64400297-chr6:64403674..64407120,4	K562	blood:
13	chr6:64342956..64345273-chr6:64406790..64408564,2	K562	blood:
14	chr6:64344073..64346131-chr6:64394565..64396308,2	K562	blood:
15	chr6:64344714..64347483-chr6:64412709..64415524,2	K562	blood:
16	chr6:64344971..64347047-chr6:64415769..64418263,2	K562	blood:
17	chr6:64283047..64284969-chr6:64418892..64421596,2	MCF-7	breast:
18	chr6:64281048..64283887-chr6:64413696..64416630,3	K562	blood:
19	chr6:64347568..64349664-chr6:64406239..64409987,3	K562	blood:
20	chr6:64400258..64402209-chr6:64406199..64408000,2	K562	blood:
21	chr6:64388160..64391006-chr6:64391117..64393015,2	MCF-7	breast:
22	chr6:64418755..64420387-chr6:64422922..64425376,2	K562	blood:
23	chr6:64388288..64391058-chr6:64393753..64395880,2	K562	blood:
24	chr6:64365652..64367564-chr6:64386875..64388430,2	K562	blood:
25	chr6:64427028..64430486-chr6:64433539..64436384,3	K562	blood:
26	chr6:64413991..64416908-chr6:64417054..64420038,2	K562	blood:
27	chr6:64427838..64430410-chr6:64430505..64432521,2	K562	blood:
28	chr6:64281737..64284624-chr6:64398462..64401172,2	MCF-7	breast:
29	chr6:64282160..64284462-chr6:64395012..64398209,3	MCF-7	breast:
30	chr6:64282444..64284956-chr6:64441888..64443717,2	MCF-7	breast:
31	chr6:64280956..64283325-chr6:64386100..64388595,2	K562	blood:
32	chr6:64408853..64410358-chr6:64415666..64417276,2	K562	blood:
33	chr6:64427028..64430486-chr6:64433539..64436384,3	K562	blood:
34	chr6:64281751..64285067-chr6:64403939..64407873,3	MCF-7	breast:
35	chr6:64375915..64378129-chr6:64385885..64387947,2	MCF-7	breast:

No data

(count:5 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	PHF3	hsa-miR-130b-3p	chr6:64424016-64424022
2	PHF3	hsa-miR-130b-3p	chr6:64424139-64424158
3	PHF3	hsa-miR-101-3p	chr6:64424270-64424290
4	PHF3	hsa-miR-130b-3p	chr6:64424003-64424023
5	PHF3	hsa-miR-101-3p	chr6:64424284-64424290

Variant related genes	Relation type
PHF3	TF binding region
PHF3	CpG island
ENSG00000266680	chromatin interactions
ENSG00000112245	chromatin interactions
ENSG00000118482	chromatin interactions

Extended variants
information (count: 2107 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:2107 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs115094502	chr6:64386847-64386848	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs554136017	chr6:64386848-64386849	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs187731839	chr6:64386870-64386871	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs192157855	chr6:64386917-64386918	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs565975853	chr6:64386933-64386934	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs113997643	chr6:64387026-64387027	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs75321040	chr6:64387034-64387035	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs558186849	chr6:64387040-64387041	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs34735537	chr6:64387084-64387085	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs534923362	chr6:64387086-64387087	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs553254984	chr6:64387181-64387182	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs115110786	chr6:64387204-64387205	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs199719001	chr6:64387206-64387207	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs541800314	chr6:64387212-64387213	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs72884679	chr6:64387262-64387263	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs149007622	chr6:64387340-64387341	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs369738474	chr6:64387371-64387372	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs543568024	chr6:64387430-64387431	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs545551164	chr6:64387495-64387496	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs565148436	chr6:64387506-64387507	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs184514952	chr6:64387520-64387521	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs555818574	chr6:64387600-64387601	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs547731935	chr6:64387612-64387613	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs200725171	chr6:64387626-64387627	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs369344433	chr6:64387627-64387628	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs77751352	chr6:64387641-64387642	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs188413229	chr6:64387665-64387666	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs137997144	chr6:64387720-64387721	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs548543345	chr6:64387724-64387725	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs144964978	chr6:64387735-64387736	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs537569901	chr6:64387754-64387755	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs192647227	chr6:64387801-64387802	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs570662094	chr6:64387816-64387817	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs559662820	chr6:64387825-64387826	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs184588903	chr6:64387840-64387841	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs574768338	chr6:64387846-64387847	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs189259134	chr6:64387878-64387879	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs556938168	chr6:64387940-64387941	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs575095349	chr6:64387949-64387950	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs191141161	chr6:64387954-64387955	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs184738673	chr6:64388051-64388052	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs545248486	chr6:64388078-64388079	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs201977192	chr6:64388122-64388123	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs577064567	chr6:64388125-64388126	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs541211756	chr6:64388132-64388133	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs559650901	chr6:64388139-64388140	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs530447160	chr6:64388150-64388151	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs147928698	chr6:64388171-64388172	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs373022855	chr6:64388173-64388174	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs530763903	chr6:64388230-64388231	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
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
Endometrioid adenocarcinoma	16974079	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
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Lung cancer	18438408	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	21364760	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Cancer	20164920	CNVD
Prostate cancer	16573809	CNVD
Ovarian cancer	19835627	CNVD
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:1262 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:64347000-64422400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr6:64351200-64405000	Weak transcription	Thymus	Thymus
3	chr6:64354000-64421200	Weak transcription	Gastric	stomach
4	chr6:64357800-64393400	Weak transcription	Placenta	Placenta
5	chr6:64365200-64387000	Weak transcription	Primary monocytes fromperipheralblood	blood
6	chr6:64365800-64409400	Weak transcription	Fetal Stomach	stomach
7	chr6:64370800-64395000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr6:64370800-64413400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr6:64371000-64394200	Weak transcription	Stomach Smooth Muscle	stomach
10	chr6:64371000-64409000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr6:64373800-64394200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr6:64373800-64394600	Weak transcription	HSMMtube	muscle
13	chr6:64373800-64394800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr6:64374000-64387200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr6:64374000-64391600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr6:64374200-64387000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr6:64374200-64393400	Weak transcription	HSMM	muscle
18	chr6:64374200-64394000	Weak transcription	NH-A	brain
19	chr6:64374200-64394200	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr6:64374200-64405800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr6:64374200-64414600	Weak transcription	HMEC	breast
22	chr6:64374400-64388800	Weak transcription	K562	blood
23	chr6:64375600-64409000	Weak transcription	Placenta Amnion	Placenta Amnion
24	chr6:64375800-64388600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
25	chr6:64377000-64394000	Weak transcription	Fetal Muscle Trunk	muscle
26	chr6:64379200-64388800	Weak transcription	Primary neutrophils fromperipheralblood	blood
27	chr6:64380600-64389400	Enhancers	Primary T helper cells fromperipheralblood	blood
28	chr6:64381200-64394200	Weak transcription	Rectal Smooth Muscle	rectum
29	chr6:64381400-64405200	Weak transcription	Brain Germinal Matrix	brain
30	chr6:64381600-64389800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr6:64382400-64387400	Enhancers	Small Intestine	intestine
32	chr6:64382400-64387600	Enhancers	Primary T helper cells PMA-I stimulated	--
33	chr6:64382600-64387600	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr6:64382600-64387600	Enhancers	Primary T helper naive cells from peripheral blood	blood
35	chr6:64382600-64387600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
36	chr6:64383000-64387200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
37	chr6:64383000-64387200	Enhancers	Primary T killer memory cells from peripheral blood	blood
38	chr6:64383000-64387600	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr6:64383200-64389000	Enhancers	Liver	Liver
40	chr6:64383200-64389200	Weak transcription	GM12878-XiMat	blood
41	chr6:64383200-64390000	Weak transcription	Primary B cells from peripheral blood	blood
42	chr6:64383400-64387600	Enhancers	Sigmoid Colon	Sigmoid Colon
43	chr6:64383400-64390200	Weak transcription	Cortex derived primary cultured neurospheres	brain
44	chr6:64383400-64394000	Weak transcription	Fetal Muscle Leg	muscle
45	chr6:64383600-64387600	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr6:64383600-64387800	Enhancers	Duodenum Mucosa	Duodenum
47	chr6:64383800-64387800	Enhancers	HepG2	liver
48	chr6:64383800-64388800	Weak transcription	Fetal Thymus	thymus
49	chr6:64383800-64388800	Weak transcription	Dnd41	blood
50	chr6:64383800-64389000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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