Variant report

Variant	nsv876741
Chromosome Location	chr3:46663372-46763839
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2359)
CpG islands
(count:3360)
Chromatin interactive
region (count:164)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2359 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr3:46684585-46684909	K562	blood:	n/a	n/a
2	ATF2	chr3:46671272-46671937	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr3:46755483-46755920	GM12878	blood:	n/a	n/a
4	ATF2	chr3:46755533-46755773	GM12878	blood:	n/a	n/a
5	ATF2	chr3:46759302-46759627	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr3:46746461-46746813	GM12878	blood:	n/a	n/a
7	ATF2	chr3:46671292-46671865	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr3:46671570-46671752	GM12878	blood:	n/a	n/a
9	ATF3	chr3:46759282-46759598	K562	blood:	n/a	n/a
10	ATF3	chr3:46671400-46671857	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF3	chr3:46759265-46759598	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr3:46671409-46671780	K562	blood:	n/a	n/a
13	ATF3	chr3:46759331-46759550	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr3:46759334-46759543	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr3:46734048-46734515	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr3:46735430-46735744	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr3:46671292-46671750	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr3:46746558-46746758	H1-hESC	embryonic stem cell:	n/a	n/a
19	BATF	chr3:46720130-46720422	GM12878	blood:	n/a	n/a
20	BATF	chr3:46720127-46720375	GM12878	blood:	n/a	n/a
21	BATF	chr3:46755589-46755797	GM12878	blood:	n/a	n/a
22	BATF	chr3:46755501-46755889	GM12878	blood:	n/a	n/a
23	BCL11A	chr3:46755551-46755755	GM12878	blood:	n/a	chr3:46755588-46755601
24	BCL11A	chr3:46755446-46755860	GM12878	blood:	n/a	chr3:46755588-46755601
25	BCL3	chr3:46755447-46755829	GM12878	blood:	n/a	chr3:46755588-46755601
26	BCLAF1	chr3:46759179-46759647	K562	blood:	n/a	n/a
27	BHLHE40	chr3:46735446-46735593	K562	blood:	n/a	n/a
28	BHLHE40	chr3:46736761-46737392	K562	blood:	n/a	n/a
29	BHLHE40	chr3:46734493-46734748	K562	blood:	n/a	n/a
30	BHLHE40	chr3:46671422-46671839	K562	blood:	n/a	chr3:46671654-46671670
31	BHLHE40	chr3:46755577-46755866	GM12878	blood:	n/a	n/a
32	BHLHE40	chr3:46734263-46734269	A549	lung:	n/a	n/a
33	BHLHE40	chr3:46736984-46737365	GM12878	blood:	n/a	n/a
34	BHLHE40	chr3:46746528-46746852	K562	blood:	n/a	n/a
35	BHLHE40	chr3:46759435-46759439	K562	blood:	n/a	n/a
36	BHLHE40	chr3:46671448-46671810	GM12878	blood:	n/a	chr3:46671654-46671670
37	BRCA1	chr3:46708976-46709045	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr3:46746485-46746854	Hela-S3	cervix:	n/a	n/a
39	BRCA1	chr3:46700658-46700720	H1-hESC	embryonic stem cell:	n/a	n/a
40	BRCA1	chr3:46759337-46759615	H1-hESC	embryonic stem cell:	n/a	n/a
41	BRCA1	chr3:46746586-46746696	HepG2	liver:	n/a	n/a
42	BRCA1	chr3:46755567-46755723	GM12878	blood:	n/a	n/a
43	BRCA1	chr3:46734876-46735076	Hela-S3	cervix:	n/a	n/a
44	BRCA1	chr3:46746601-46746847	H1-hESC	embryonic stem cell:	n/a	n/a
45	CBX3	chr3:46759328-46759544	K562	blood:	n/a	n/a
46	CBX3	chr3:46693497-46693764	K562	blood:	n/a	n/a
47	CBX3	chr3:46759289-46759662	K562	blood:	n/a	n/a
48	CBX3	chr3:46671216-46671805	K562	blood:	n/a	n/a
49	CCNT2	chr3:46734819-46735516	K562	blood:	n/a	n/a
50	CCNT2	chr3:46671310-46671777	K562	blood:	n/a	n/a

(count:3360 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:46730941-46730991	AG09319	gingival:	n/a
2	chr3:46735009-46735059	MCF10A-Er-Src	breast:	n/a
3	chr3:46687388-46687438	HNPCEpiC	eye:	n/a
4	chr3:46742865-46742915	NB4	blood:	n/a
5	chr3:46759096-46759146	HNPCEpiC	eye:	n/a
6	chr3:46730941-46730991	AG09319	gingival:	n/a
7	chr3:46735009-46735059	MCF10A-Er-Src	breast:	n/a
8	chr3:46687388-46687438	HNPCEpiC	eye:	n/a
9	chr3:46742865-46742915	NB4	blood:	n/a
10	chr3:46759096-46759146	HNPCEpiC	eye:	n/a
11	chr3:46718369-46718419	AoSMC	blood vessel:	n/a
12	chr3:46734995-46735045	AG04450	lung:	fetal
13	chr3:46739004-46739054	ovcar-3	ovarian:	n/a
14	chr3:46743199-46743249	HAEpiC	amniotic membrane:	n/a
15	chr3:46735154-46735204	K562	blood:	n/a
16	chr3:46759698-46759748	AG09309	skin:	n/a
17	chr3:46747930-46747980	AG09309	skin:	n/a
18	chr3:46735154-46735204	Caco-2	colon:	n/a
19	chr3:46735152-46735202	MCF10A-Er-Src	breast:	n/a
20	chr3:46733475-46733525	SK-N-MC	brain:	n/a
21	chr3:46759335-46759385	LNCaP	prostate:	n/a
22	chr3:46742491-46742541	HNPCEpiC	eye:	n/a
23	chr3:46742491-46742541	BE2_C	brain:	n/a
24	chr3:46719834-46719884	HRCEpiC	kidney:	n/a
25	chr3:46735801-46735851	ECC-1	luminal epithelium:	n/a
26	chr3:46759472-46759522	BJ	skin:	n/a
27	chr3:46742865-46742915	CMK	blood:	n/a
28	chr3:46735338-46735388	HCM	heart:	n/a
29	chr3:46759656-46759706	AG04449	skin:	fetal
30	chr3:46752152-46752202	AG04449	skin:	fetal
31	chr3:46752152-46752202	NH-A	brain:	n/a
32	chr3:46734393-46734443	Jurkat	blood:	n/a
33	chr3:46759475-46759525	ProgFib	skin:	n/a
34	chr3:46752152-46752202	U87	brain:	n/a
35	chr3:46735152-46735202	NHBE	bronchial:	n/a
36	chr3:46671563-46671613	GM12891	blood:	n/a
37	chr3:46759449-46759499	Hepatocyte	liver:	n/a
38	chr3:46735454-46735504	HEK293	kidney:	embryo
39	chr3:46735801-46735851	HNPCEpiC	eye:	n/a
40	chr3:46704065-46704115	NHBE	bronchial:	n/a
41	chr3:46734995-46735045	ECC-1	luminal epithelium:	n/a
42	chr3:46735319-46735369	IMR90	lung:	fetal
43	chr3:46735782-46735832	AG04450	lung:	fetal
44	chr3:46759472-46759522	GM06990	blood:	n/a
45	chr3:46669290-46669340	HCT-116	colon:	n/a
46	chr3:46735695-46735745	AoSMC	blood vessel:	n/a
47	chr3:46735782-46735832	HPAEpiC	pulmonary alveolar:	n/a
48	chr3:46704065-46704115	AoSMC	blood vessel:	n/a
49	chr3:46704065-46704115	MCF-7	breast:	n/a
50	chr3:46742703-46742753	AG10803	skin:	n/a

(count:164 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr3:46735218..46737600-chr3:46738787..46741218,2	K562	blood:
2	chr3:46694367..46696784-chr3:46700533..46702461,2	K562	blood:
3	chr3:46746227..46747136-chr3:46797879..46798830,2	K562	blood:
4	chr3:46707530..46709982-chr3:46711149..46714588,3	K562	blood:
5	chr3:46723220..46725442-chr3:46727287..46728789,2	K562	blood:
6	chr3:46711861..46714568-chr3:46714913..46719583,6	K562	blood:
7	chr3:46700528..46705296-chr3:46732661..46735807,9	MCF-7	breast:
8	chr3:46733050..46735013-chr3:46736523..46739104,3	K562	blood:
9	chr3:46746166..46747117-chr3:46950364..46951554,3	MCF-7	breast:
10	chr3:46748228..46751973-chr3:46757589..46759527,3	MCF-7	breast:
11	chr3:46679929..46681970-chr3:46683200..46686358,3	MCF-7	breast:
12	chr3:46729365..46731831-chr3:46732714..46735067,2	K562	blood:
13	chr3:46735288..46735975-chr3:46746178..46746698,2	K562	blood:
14	chr3:46503439..46504291-chr3:46671319..46672034,3	K562	blood:
15	chr3:46634709..46635296-chr3:46671423..46672075,2	MCF-7	breast:
16	chr3:46736001..46738313-chr3:46739420..46741660,3	MCF-7	breast:
17	chr3:46734355..46735316-chr5:133512715..133513418,2	Hela-S3	cervix:
18	chr3:46719842..46724126-chr3:46725182..46728551,5	MCF-7	breast:
19	chr3:46676467..46678171-chr3:46680903..46682771,2	K562	blood:
20	chr3:46670811..46674020-chr3:46675061..46678300,4	K562	blood:
21	chr3:46720846..46722573-chr3:46724433..46726635,2	MCF-7	breast:
22	chr3:46700787..46702922-chr3:46710281..46712322,2	K562	blood:
23	chr3:46650273..46651172-chr3:46707945..46708857,6	MCF-7	breast:
24	chr3:46503615..46504280-chr3:46671186..46672162,2	MCF-7	breast:
25	chr3:46706471..46710183-chr3:46732042..46737071,8	MCF-7	breast:
26	chr3:46693588..46695297-chr3:46696531..46698308,2	MCF-7	breast:
27	chr3:46730164..46732483-chr3:46734488..46736983,2	MCF-7	breast:
28	chr3:46702436..46704815-chr3:46735975..46737913,2	MCF-7	breast:
29	chr3:46703608..46706840-chr3:46708905..46711367,3	K562	blood:
30	chr3:46733775..46736386-chr3:46933231..46935509,2	MCF-7	breast:
31	chr3:46717709..46719534-chr3:46734745..46736639,2	MCF-7	breast:
32	chr3:46697148..46699057-chr3:46702525..46705499,2	K562	blood:
33	chr3:46671153..46671844-chr3:46736764..46737267,2	MCF-7	breast:
34	chr3:46751695..46753844-chr3:46756302..46759946,5	K562	blood:
35	chr3:46746480..46747149-chr3:46935659..46936387,2	MCF-7	breast:
36	chr3:46713668..46715350-chr3:46724195..46726906,2	MCF-7	breast:
37	chr3:46529871..46530872-chr3:46670590..46672462,23	K562	blood:
38	chr3:46723220..46725442-chr3:46727287..46728789,2	K562	blood:
39	chr3:46704379..46706248-chr3:46709727..46711417,3	K562	blood:
40	chr3:46751695..46753830-chr3:46756302..46759551,4	K562	blood:
41	chr3:46707530..46709982-chr3:46711149..46714588,3	K562	blood:
42	chr3:46734988..46739707-chr3:46741491..46746249,8	K562	blood:
43	chr3:46720178..46722487-chr3:46787613..46789601,2	K562	blood:
44	chr3:46676467..46678171-chr3:46680903..46682771,2	K562	blood:
45	chr3:46735218..46737600-chr3:46738787..46741218,2	K562	blood:
46	chr3:46653817..46656783-chr3:46662139..46665039,2	K562	blood:
47	chr3:46733050..46735013-chr3:46736523..46739104,3	K562	blood:
48	chr3:46746174..46747036-chr3:46933635..46934581,2	MCF-7	breast:
49	chr3:46724809..46726431-chr3:46731600..46733617,2	K562	blood:
50	chr3:46742077..46744445-chr3:46744916..46748199,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMIE-1	chr3:46667272-46667698	NONHSAT089452

No data

Variant related genes	Relation type
ALS2CL	TF binding region
ENSG00000251967	TF binding region
ENSG00000256354	TF binding region
TMIE	TF binding region
PRSS50	TF binding region
ALS2CL	CpG island
ENSG00000251967	CpG island
ENSG00000256354	CpG island
TMIE	CpG island
PRSS50	CpG island
ENSG00000241186	chromatin interactions
ENSG00000270006	chromatin interactions
ENSG00000260456	chromatin interactions
ENSG00000206549	chromatin interactions
ENSG00000261603	chromatin interactions
ENSG00000160796	chromatin interactions
ENSG00000101558	chromatin interactions
ENSG00000181585	chromatin interactions
ENSG00000160801	chromatin interactions
ENSG00000201558	chromatin interactions
ENSG00000186432	chromatin interactions
ENSG00000006062	chromatin interactions
ENSG00000178038	chromatin interactions
ENSG00000160799	chromatin interactions
ENSG00000229320	chromatin interactions
ENSG00000264306	chromatin interactions
ENSG00000113558	chromatin interactions

Extended variants
information (count: 4091 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:4091 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9817414	chr3:46663372-46663373	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs199813650	chr3:46663422-46663423	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs188220229	chr3:46663465-46663466	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs528979048	chr3:46663503-46663504	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs34762071	chr3:46663505-46663506	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs397761676	chr3:46663507-46663508	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs550658867	chr3:46663530-46663531	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs377403845	chr3:46663540-46663541	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs201533945	chr3:46663585-46663586	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs377653112	chr3:46663595-46663596	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs374644574	chr3:46663596-46663597	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs13095773	chr3:46663597-46663598	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs112322237	chr3:46663604-46663605	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs187408145	chr3:46663616-46663617	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs78647705	chr3:46663618-46663619	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs112874687	chr3:46663621-46663622	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs551730272	chr3:46663644-46663645	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs567153695	chr3:46663695-46663696	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs534253819	chr3:46663701-46663702	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs147927312	chr3:46663703-46663704	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs567519581	chr3:46663721-46663722	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs537872707	chr3:46663744-46663745	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs532299722	chr3:46663798-46663799	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs556191064	chr3:46663808-46663809	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs375531337	chr3:46663823-46663824	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs545584210	chr3:46663832-46663833	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs191419817	chr3:46663842-46663843	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs372587998	chr3:46663843-46663844	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs182179732	chr3:46663848-46663849	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs562029800	chr3:46663875-46663876	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs528863727	chr3:46663887-46663888	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs113776280	chr3:46663888-46663889	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs186264771	chr3:46663893-46663894	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs149928593	chr3:46663898-46663899	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs116181656	chr3:46663915-46663916	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs551932529	chr3:46663999-46664000	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs566987738	chr3:46664019-46664020	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs79637303	chr3:46664031-46664032	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs190375767	chr3:46664096-46664097	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs567623531	chr3:46664126-46664127	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs537806485	chr3:46664154-46664155	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs556178853	chr3:46664155-46664156	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs571404120	chr3:46664181-46664182	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs114317113	chr3:46664214-46664215	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs182726964	chr3:46664223-46664224	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs572916688	chr3:46664242-46664243	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs534012675	chr3:46664264-46664265	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs555325041	chr3:46664349-46664350	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs201334323	chr3:46664351-46664352	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs35745268	chr3:46664384-46664385	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
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
Glioblastoma multiforme	21080181	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
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Kartagener syndrome	16639409	CNVD
Biliary cancer	19435499	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Breast cancer	21509527	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22032731	CNVD
Non-small cell lung cancer	20864512	CNVD
Colorectal cancer	16912164	CNVD
Non-small cell lung cancer	19010865	CNVD
Colorectal cancer	16272173	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute myeloid leukemia	17268525	CNVD
Salivary gland tumor	18059337	CNVD
Gastric cancer	16891809	CNVD
Night blindness	17160897	CNVD
Cancer	17160897	CNVD
Breast cancer	20409316	CNVD
Lung cancer	17297452	CNVD
Multiple myeloma	16616336	CNVD
Effusion lymphoma	18079361	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Urothelial cell carcinoma	18451213	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Melanoma	17363583	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Adrenocortical carcinoma	18281524	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian cancer	21781307	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:2391 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:46651600-46671200	Weak transcription	Right Atrium	heart
2	chr3:46661600-46670200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr3:46661800-46666200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr3:46661800-46666600	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr3:46661800-46670200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr3:46662000-46666600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr3:46662200-46666600	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr3:46662200-46670400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr3:46662400-46666200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr3:46662400-46666600	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr3:46665400-46665800	Enhancers	Fetal Intestine Large	intestine
12	chr3:46665800-46666000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr3:46665800-46666200	Weak transcription	Fetal Intestine Large	intestine
14	chr3:46666200-46667000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
15	chr3:46666200-46667600	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr3:46666200-46669200	Enhancers	Fetal Intestine Large	intestine
17	chr3:46666600-46666800	Enhancers	Brain Inferior Temporal Lobe	brain
18	chr3:46666600-46667000	Enhancers	H1 Cell Line	embryonic stem cell
19	chr3:46666600-46667000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr3:46666600-46667000	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr3:46666600-46667000	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr3:46666600-46667000	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr3:46666600-46667000	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr3:46666600-46667000	Enhancers	Brain Angular Gyrus	brain
25	chr3:46666600-46667000	Enhancers	Brain Cingulate Gyrus	brain
26	chr3:46666600-46667000	Enhancers	Left Ventricle	heart
27	chr3:46666600-46667200	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr3:46666600-46667200	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr3:46666600-46667200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr3:46666600-46667600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr3:46666600-46669200	Enhancers	Rectal Mucosa Donor 29	rectum
32	chr3:46666600-46669200	Enhancers	Rectal Mucosa Donor 31	rectum
33	chr3:46666600-46669400	Enhancers	Fetal Intestine Small	intestine
34	chr3:46666600-46670800	Enhancers	Fetal Muscle Leg	muscle
35	chr3:46666800-46667000	Enhancers	Brain Hippocampus Middle	brain
36	chr3:46667000-46667400	Weak transcription	Left Ventricle	heart
37	chr3:46667000-46669400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
38	chr3:46667000-46669800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr3:46667000-46669800	Weak transcription	HUES6 Cell Line	embryonic stem cell
40	chr3:46667000-46670000	Weak transcription	H1 Cell Line	embryonic stem cell
41	chr3:46667000-46670000	Weak transcription	HUES48 Cell Line	embryonic stem cell
42	chr3:46667000-46670000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
43	chr3:46667000-46670000	Weak transcription	Brain Angular Gyrus	brain
44	chr3:46667000-46670000	Weak transcription	Brain Cingulate Gyrus	brain
45	chr3:46667200-46669800	Weak transcription	HUES64 Cell Line	embryonic stem cell
46	chr3:46667200-46669800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr3:46667200-46670000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
48	chr3:46667400-46667600	Enhancers	Left Ventricle	heart
49	chr3:46667400-46669200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr3:46667400-46669400	Enhancers	Sigmoid Colon	Sigmoid Colon

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