Variant report

Variant	nsv428080
Chromosome Location	chr3:17367870-17539943
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1278)
CpG islands
(count:61)
Chromatin interactive
region (count:92)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1278 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:17472416-17472770	K562	blood:	n/a	n/a
2	ARID3A	chr3:17484122-17484922	K562	blood:	n/a	n/a
3	ARID3A	chr3:17506407-17506512	K562	blood:	n/a	n/a
4	ARID3A	chr3:17414297-17414619	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:17462080-17462754	HepG2	liver:	n/a	n/a
6	ARID3A	chr3:17486399-17486776	K562	blood:	n/a	n/a
7	ARID3A	chr3:17454500-17454738	HepG2	liver:	n/a	n/a
8	ATF1	chr3:17484669-17484932	K562	blood:	n/a	n/a
9	ATF1	chr3:17486434-17486698	K562	blood:	n/a	n/a
10	ATF1	chr3:17375418-17375715	K562	blood:	n/a	n/a
11	ATF1	chr3:17472550-17472822	K562	blood:	n/a	n/a
12	ATF1	chr3:17380747-17381109	K562	blood:	n/a	n/a
13	ATF1	chr3:17410725-17410748	K562	blood:	n/a	n/a
14	ATF1	chr3:17520229-17520516	K562	blood:	n/a	n/a
15	ATF1	chr3:17484018-17484387	K562	blood:	n/a	n/a
16	ATF2	chr3:17440529-17441152	GM12878	blood:	n/a	n/a
17	ATF2	chr3:17440604-17441083	GM12878	blood:	n/a	n/a
18	ATF3	chr3:17484191-17484365	K562	blood:	n/a	n/a
19	ATF3	chr3:17520058-17520526	A549	lung:	n/a	n/a
20	ATF3	chr3:17520011-17520619	A549	lung:	n/a	n/a
21	ATF3	chr3:17486331-17486754	K562	blood:	n/a	n/a
22	ATF3	chr3:17484214-17484440	K562	blood:	n/a	n/a
23	BACH1	chr3:17539622-17539654	K562	blood:	n/a	n/a
24	BACH1	chr3:17473751-17474065	K562	blood:	n/a	chr3:17473906-17473920
25	BACH1	chr3:17474299-17474445	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr3:17473755-17474077	H1-hESC	embryonic stem cell:	n/a	chr3:17473906-17473920
27	BATF	chr3:17440687-17441050	GM12878	blood:	n/a	n/a
28	BATF	chr3:17440584-17441027	GM12878	blood:	n/a	n/a
29	BCL11A	chr3:17440655-17441034	GM12878	blood:	n/a	chr3:17440792-17440801
30	BCL11A	chr3:17440636-17441099	GM12878	blood:	n/a	chr3:17440792-17440801
31	BCL11A	chr3:17378630-17378839	GM12878	blood:	n/a	n/a
32	BCL3	chr3:17520027-17520714	A549	lung:	n/a	n/a
33	BCLAF1	chr3:17440619-17441234	GM12878	blood:	n/a	chr3:17440792-17440801
34	BCLAF1	chr3:17440538-17441322	GM12878	blood:	n/a	chr3:17440792-17440801
35	BHLHE40	chr3:17428087-17428202	K562	blood:	n/a	n/a
36	BHLHE40	chr3:17520199-17520344	HepG2	liver:	n/a	n/a
37	BHLHE40	chr3:17462222-17462436	K562	blood:	n/a	n/a
38	BHLHE40	chr3:17462223-17462521	HepG2	liver:	n/a	n/a
39	BHLHE40	chr3:17440644-17441042	GM12878	blood:	n/a	n/a
40	BHLHE40	chr3:17484668-17485011	K562	blood:	n/a	n/a
41	BHLHE40	chr3:17380693-17381093	K562	blood:	n/a	n/a
42	BRCA1	chr3:17454624-17454755	HepG2	liver:	n/a	n/a
43	BRCA1	chr3:17519940-17520632	Hela-S3	cervix:	n/a	n/a
44	CBX3	chr3:17484569-17485167	K562	blood:	n/a	n/a
45	CBX3	chr3:17484048-17484463	K562	blood:	n/a	n/a
46	CCNT2	chr3:17380766-17381064	K562	blood:	n/a	n/a
47	CCNT2	chr3:17472494-17472658	K562	blood:	n/a	n/a
48	CCNT2	chr3:17410588-17410779	K562	blood:	n/a	n/a
49	CEBPB	chr3:17533154-17533417	IMR90	lung:	n/a	n/a
50	CEBPB	chr3:17475244-17475454	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:17375660-17375710	NHDF-neo	bronchial:	n/a
2	chr3:17375660-17375710	PFSK-1	brain:	n/a
3	chr3:17375660-17375710	SK-N-SH	brain:	n/a
4	chr3:17375660-17375710	PrEC	prostate:	n/a
5	chr3:17375660-17375710	HUVEC	blood vessel:	n/a
6	chr3:17375660-17375710	HAEpiC	amniotic membrane:	n/a
7	chr3:17375660-17375710	SKMC	muscle:	n/a
8	chr3:17375660-17375710	Jurkat	blood:	n/a
9	chr3:17375660-17375710	CMK	blood:	n/a
10	chr3:17375660-17375710	ECC-1	luminal epithelium:	n/a
11	chr3:17375660-17375710	AG09309	skin:	n/a
12	chr3:17375660-17375710	MCF-7	breast:	n/a
13	chr3:17375660-17375710	PANC-1	pancreas:	n/a
14	chr3:17375660-17375710	AG09319	gingival:	n/a
15	chr3:17375660-17375710	GM12891	blood:	n/a
16	chr3:17375660-17375710	AoSMC	blood vessel:	n/a
17	chr3:17375660-17375710	K562	blood:	n/a
18	chr3:17375660-17375710	HCT-116	colon:	n/a
19	chr3:17375660-17375710	NH-A	brain:	n/a
20	chr3:17375660-17375710	HRE	kidney:	n/a
21	chr3:17375660-17375710	HepG2	liver:	n/a
22	chr3:17375660-17375710	IMR90	lung:	fetal
23	chr3:17375660-17375710	SK-N-SH_RA	brain:	n/a
24	chr3:17375660-17375710	NHBE	bronchial:	n/a
25	chr3:17375660-17375710	RPTEC	kidney:	n/a
26	chr3:17375660-17375710	GM06990	blood:	n/a
27	chr3:17375660-17375710	HIPEpiC	eye:	n/a
28	chr3:17375660-17375710	T-47D	breast:	n/a
29	chr3:17375660-17375710	Caco-2	colon:	n/a
30	chr3:17375660-17375710	A549	lung:	n/a
31	chr3:17375660-17375710	ProgFib	skin:	n/a
32	chr3:17375660-17375710	HNPCEpiC	eye:	n/a
33	chr3:17375660-17375710	GM12878	blood:	n/a
34	chr3:17375660-17375710	Hela-S3	cervix:	n/a
35	chr3:17375660-17375710	ovcar-3	ovarian:	n/a
36	chr3:17375660-17375710	NT2-D1	testis:	n/a
37	chr3:17375660-17375710	BE2_C	brain:	n/a
38	chr3:17375660-17375710	HEEpiC	esophagus:	n/a
39	chr3:17375660-17375710	U87	brain:	n/a
40	chr3:17375660-17375710	BJ	skin:	n/a
41	chr3:17375660-17375710	Hepatocyte	liver:	n/a
42	chr3:17375660-17375710	GM12892	blood:	n/a
43	chr3:17375660-17375710	SK-N-MC	brain:	n/a
44	chr3:17375660-17375710	HEK293	kidney:	embryo
45	chr3:17375660-17375710	AG10803	skin:	n/a
46	chr3:17375660-17375710	LNCaP	prostate:	n/a
47	chr3:17375660-17375710	NB4	blood:	n/a
48	chr3:17375660-17375710	GM19239	blood:	n/a
49	chr3:17375660-17375710	SAEC	small airway:	n/a
50	chr3:17375660-17375710	HCF	heart:	n/a

(count:92 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:17356582..17359217-chr3:17376177..17378852,2	K562	blood:
2	chr3:17514624..17515516-chr3:17727784..17728694,2	MCF-7	breast:
3	chr3:17459732..17461276-chr3:17463158..17466015,2	MCF-7	breast:
4	chr3:17468044..17471008-chr3:17472912..17474863,2	MCF-7	breast:
5	chr3:17300330..17301004-chr3:17455425..17455933,2	K562	blood:
6	chr3:17396587..17398372-chr3:17401849..17403635,2	K562	blood:
7	chr3:17299624..17302842-chr3:17453304..17456180,3	MCF-7	breast:
8	chr3:17455901..17458583-chr3:17462176..17465120,2	K562	blood:
9	chr3:17520321..17522399-chr3:17522640..17525341,2	K562	blood:
10	chr3:17426084..17429101-chr3:17432439..17434660,3	MCF-7	breast:
11	chr3:17322980..17323870-chr3:17472180..17472688,2	K562	blood:
12	chr3:17415575..17418642-chr3:17419331..17422264,3	MCF-7	breast:
13	chr3:17468044..17471008-chr3:17472912..17474863,2	MCF-7	breast:
14	chr3:17518313..17520629-chr3:17521648..17524012,2	MCF-7	breast:
15	chr3:17497521..17499126-chr3:17503539..17506247,2	MCF-7	breast:
16	chr3:17507187..17509434-chr3:17516355..17517975,2	MCF-7	breast:
17	chr3:17416222..17418689-chr3:177528351..177530087,2	MCF-7	breast:
18	chr3:17455901..17458583-chr3:17462176..17465120,2	K562	blood:
19	chr3:17518313..17520629-chr3:17521648..17524012,2	MCF-7	breast:
20	chr3:17472374..17472992-chr3:18020408..18021268,3	MCF-7	breast:
21	chr3:17378116..17380308-chr3:17381521..17383139,2	MCF-7	breast:
22	chr3:17366087..17369722-chr3:17373833..17377083,3	K562	blood:
23	chr3:17371090..17372761-chr3:17372813..17375447,2	K562	blood:
24	chr3:17348477..17349876-chr3:17454198..17455145,8	MCF-7	breast:
25	chr3:17447638..17450232-chr3:17453263..17456160,3	K562	blood:
26	chr3:17352641..17354178-chr3:17468928..17471565,2	MCF-7	breast:
27	chr3:17472087..17473109-chr3:17882519..17883281,4	MCF-7	breast:
28	chr3:17472510..17474069-chr3:17729758..17732549,2	K562	blood:
29	chr3:17454364..17456492-chr3:17782379..17784281,3	MCF-7	breast:
30	chr3:17378116..17380308-chr3:17381521..17383139,2	MCF-7	breast:
31	chr3:17299444..17301149-chr3:17449495..17452150,2	K562	blood:
32	chr3:17379961..17382534-chr3:17388424..17391231,2	MCF-7	breast:
33	chr3:17515336..17515883-chr3:17728199..17729050,2	MCF-7	breast:
34	chr3:17300074..17301498-chr3:17454119..17455081,6	K562	blood:
35	chr3:17396587..17398372-chr3:17401849..17403635,2	K562	blood:
36	chr3:17484813..17486609-chr3:17782332..17783917,2	MCF-7	breast:
37	chr3:17300011..17301671-chr3:17454009..17455084,9	MCF-7	breast:
38	chr3:17368348..17370643-chr3:17400636..17402595,2	MCF-7	breast:
39	chr3:17472682..17474282-chr3:17477579..17479223,2	K562	blood:
40	chr3:17507187..17509434-chr3:17516355..17517975,2	MCF-7	breast:
41	chr3:17426084..17429101-chr3:17432439..17434660,3	MCF-7	breast:
42	chr3:17472273..17475803-chr3:17482384..17484152,3	K562	blood:
43	chr3:17374826..17377586-chr3:17377790..17379356,2	K562	blood:
44	chr3:17454330..17455065-chr3:17882486..17883391,2	K562	blood:
45	chr3:17484535..17486940-chr3:17491207..17493318,2	MCF-7	breast:
46	chr3:17472682..17474282-chr3:17477579..17479223,2	K562	blood:
47	chr3:17379266..17381414-chr3:17386498..17389458,2	K562	blood:
48	chr3:17396023..17398371-chr3:17401669..17406284,4	K562	blood:
49	chr3:17472273..17475803-chr3:17482384..17484152,3	K562	blood:
50	chr3:17472139..17473280-chr3:17881966..17883098,4	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DAZL-5	chr3:17382147-17382187	NONHSAT088543
2	lnc-DAZL-5	chr3:17379941-17380067	NONHSAT088543
3	lnc-DAZL-5	chr3:17378881-17379128	NONHSAT088543
4	lnc-PLCL2-8	chr3:17506642-17507002	NONHSAT088548
5	lnc-PLCL2-7	chr3:17374618-17374923	NONHSAT088542
6	lnc-DAZL-5	chr3:17413567-17413626	NONHSAT088543

No data

Variant related genes	Relation type
TBC1D5	TF binding region
ENSG00000231780	TF binding region
ENSG00000227309	TF binding region
TBC1D5	CpG island
ENSG00000231780	CpG island
ENSG00000227309	CpG island
ENSG00000131374	chromatin interactions
ENSG00000231780	chromatin interactions

Extended variants
information (count: 6188 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:6188 , 50 per page) page: 1 2 3 4 5 6 7 ... 124

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs141079794	chr3:17367927-17367928	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs115268859	chr3:17367992-17367993	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs537727700	chr3:17368004-17368005	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs557656816	chr3:17368019-17368020	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs528471633	chr3:17368027-17368028	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs562275752	chr3:17368137-17368138	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs2596652	chr3:17368197-17368198	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs150278130	chr3:17368234-17368235	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs537161460	chr3:17368236-17368237	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs550331571	chr3:17368247-17368248	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs567124704	chr3:17368254-17368255	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs536508226	chr3:17368329-17368330	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs552984747	chr3:17368331-17368332	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs180869618	chr3:17368334-17368335	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs143748001	chr3:17368340-17368341	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs138889916	chr3:17368374-17368375	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs558620238	chr3:17368389-17368390	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs73145814	chr3:17368425-17368426	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs541258981	chr3:17368430-17368431	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs542610974	chr3:17368451-17368452	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs186440491	chr3:17368456-17368457	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs79260627	chr3:17368480-17368481	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs78466193	chr3:17368518-17368519	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs528815800	chr3:17368527-17368528	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs17043404	chr3:17368550-17368551	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs116517048	chr3:17368596-17368597	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs191813763	chr3:17368650-17368651	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs531766432	chr3:17368653-17368654	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs550667513	chr3:17368668-17368669	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs543335811	chr3:17368708-17368709	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs563208646	chr3:17368778-17368779	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs371938194	chr3:17368786-17368787	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs183727332	chr3:17368802-17368803	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs143255264	chr3:17368807-17368808	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs546803873	chr3:17368817-17368818	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs566641198	chr3:17368838-17368839	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs538951496	chr3:17368868-17368869	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs558559743	chr3:17369038-17369039	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs372370536	chr3:17369096-17369097	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs575315672	chr3:17369170-17369171	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs537900710	chr3:17369181-17369182	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs186631653	chr3:17369211-17369212	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs574501996	chr3:17369212-17369213	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs115478507	chr3:17369235-17369236	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs191755572	chr3:17369241-17369242	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs573426879	chr3:17369257-17369258	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs545297697	chr3:17369258-17369259	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs564892737	chr3:17369273-17369274	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs113468790	chr3:17369275-17369276	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs550835355	chr3:17369287-17369288	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	21364760	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	17133270	CNVD
Ovarian cancer	21781307	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Bipolar disorder	19114987	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1331 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:17298800-17373000	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr3:17330800-17381400	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr3:17333400-17372000	Weak transcription	Liver	Liver
4	chr3:17333400-17376000	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr3:17339400-17442200	Weak transcription	Fetal Intestine Small	intestine
6	chr3:17344400-17439000	Weak transcription	Aorta	Aorta
7	chr3:17352000-17377600	Weak transcription	Dnd41	blood
8	chr3:17352200-17370800	Weak transcription	Fetal Lung	lung
9	chr3:17354800-17381600	Weak transcription	Ovary	ovary
10	chr3:17356200-17412800	Weak transcription	Left Ventricle	heart
11	chr3:17356800-17390000	Weak transcription	Fetal Muscle Trunk	muscle
12	chr3:17358000-17377600	Weak transcription	Adipose Nuclei	Adipose
13	chr3:17362000-17376200	Weak transcription	Fetal Kidney	kidney
14	chr3:17362800-17382200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr3:17364600-17369600	Weak transcription	Primary B cells from peripheral blood	blood
16	chr3:17364600-17387600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr3:17364800-17370000	Weak transcription	Monocytes-CD14+_RO01746	blood
18	chr3:17364800-17375400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
19	chr3:17364800-17381800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
20	chr3:17365000-17377800	Weak transcription	Fetal Heart	heart
21	chr3:17365200-17383400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr3:17365400-17390000	Weak transcription	GM12878-XiMat	blood
23	chr3:17365600-17372400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr3:17365600-17374200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr3:17365600-17377200	Weak transcription	Primary T cells from cord blood	blood
26	chr3:17365600-17413000	Weak transcription	Primary hematopoietic stem cells	blood
27	chr3:17366800-17372400	Strong transcription	Primary B cells from cord blood	blood
28	chr3:17368200-17368400	Enhancers	Psoas Muscle	Psoas
29	chr3:17368400-17381600	Weak transcription	Psoas Muscle	Psoas
30	chr3:17368400-17384200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr3:17368600-17371400	Weak transcription	Fetal Muscle Leg	muscle
32	chr3:17369000-17370200	Weak transcription	Primary neutrophils fromperipheralblood	blood
33	chr3:17369600-17370000	Strong transcription	Primary B cells from peripheral blood	blood
34	chr3:17370000-17370800	Strong transcription	Monocytes-CD14+_RO01746	blood
35	chr3:17370000-17406200	Weak transcription	Primary B cells from peripheral blood	blood
36	chr3:17370200-17371800	Enhancers	Primary neutrophils fromperipheralblood	blood
37	chr3:17370800-17411000	Weak transcription	Monocytes-CD14+_RO01746	blood
38	chr3:17372400-17372800	ZNF genes & repeats	Primary B cells from cord blood	blood
39	chr3:17372400-17372800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr3:17372400-17410600	Weak transcription	Primary monocytes fromperipheralblood	blood
41	chr3:17372800-17374200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr3:17372800-17375800	Strong transcription	Primary B cells from cord blood	blood
43	chr3:17374200-17375000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr3:17374200-17375800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr3:17375000-17380600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr3:17375200-17375600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr3:17375200-17376000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
48	chr3:17375200-17376200	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr3:17375200-17376200	Enhancers	K562	blood
50	chr3:17375400-17376000	Enhancers	HUES48 Cell Line	embryonic stem cell

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