Variant report

Variant	nsv536561
Chromosome Location	chr3:47891634-48019462
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1265)
CpG islands
(count:734)
Chromatin interactive
region (count:66)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:12)

(count:1265 , 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	chr3:47991572-47992014	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:48006096-48006657	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:48003444-48004114	K562	blood:	n/a	n/a
4	ARID3A	chr3:47891558-47891772	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:47912920-47913184	K562	blood:	n/a	n/a
6	ARID3A	chr3:47995961-47996755	HepG2	liver:	n/a	n/a
7	ARID3A	chr3:47952454-47952470	K562	blood:	n/a	n/a
8	ATF1	chr3:47914032-47914186	K562	blood:	n/a	n/a
9	ATF1	chr3:47912838-47913288	K562	blood:	n/a	n/a
10	ATF2	chr3:47892483-47892944	GM12878	blood:	n/a	n/a
11	ATF2	chr3:47891515-47892057	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr3:47891643-47892403	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr3:48003559-48003759	K562	blood:	n/a	n/a
14	BACH1	chr3:47951220-47951243	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr3:48018552-48018725	K562	blood:	n/a	n/a
16	BACH1	chr3:47952274-47952594	K562	blood:	n/a	n/a
17	BACH1	chr3:47952257-47952646	H1-hESC	embryonic stem cell:	n/a	n/a
18	BCL3	chr3:47892185-47892595	A549	lung:	n/a	n/a
19	BCL3	chr3:47891139-47893184	K562	blood:	n/a	n/a
20	BCL3	chr3:47891382-47893204	A549	lung:	n/a	n/a
21	BCL3	chr3:47891755-47892988	GM12878	blood:	n/a	n/a
22	BCL3	chr3:47891647-47892404	K562	blood:	n/a	n/a
23	BCLAF1	chr3:47891764-47892275	K562	blood:	n/a	n/a
24	BCLAF1	chr3:47984762-47985166	GM12878	blood:	n/a	n/a
25	BCLAF1	chr3:47891819-47892330	GM12878	blood:	n/a	n/a
26	BHLHE40	chr3:48005785-48005906	K562	blood:	n/a	n/a
27	BHLHE40	chr3:47991948-47992285	GM12878	blood:	n/a	n/a
28	BHLHE40	chr3:47914856-47914863	A549	lung:	n/a	n/a
29	BHLHE40	chr3:48003402-48003990	K562	blood:	n/a	n/a
30	BHLHE40	chr3:47912915-47913276	K562	blood:	n/a	n/a
31	BRCA1	chr3:47991218-47991257	GM12878	blood:	n/a	n/a
32	CBX3	chr3:47912466-47913365	K562	blood:	n/a	n/a
33	CBX3	chr3:48003163-48003744	K562	blood:	n/a	n/a
34	CCNT2	chr3:48003822-48004364	K562	blood:	n/a	n/a
35	CCNT2	chr3:47892260-47892693	K562	blood:	n/a	n/a
36	CCNT2	chr3:47914670-47914690	K562	blood:	n/a	n/a
37	CCNT2	chr3:47891145-47891643	K562	blood:	n/a	n/a
38	CEBPB	chr3:47935519-47935646	K562	blood:	n/a	n/a
39	CEBPB	chr3:47911459-47911636	A549	lung:	n/a	chr3:47911525-47911538 chr3:47911525-47911536
40	CEBPB	chr3:48006139-48006654	HepG2	liver:	n/a	chr3:48006182-48006195 chr3:48006478-48006489
41	CEBPB	chr3:47979849-47980073	K562	blood:	n/a	chr3:47979919-47979930
42	CEBPB	chr3:47931924-47932402	H1-hESC	embryonic stem cell:	n/a	chr3:47932017-47932028 chr3:47932018-47932027 chr3:47932016-47932027
43	CEBPB	chr3:47942799-47943145	HepG2	liver:	n/a	chr3:47942971-47942982
44	CEBPB	chr3:47931933-47932165	HepG2	liver:	n/a	chr3:47932017-47932028 chr3:47932018-47932027 chr3:47932016-47932027
45	CEBPB	chr3:47942921-47942998	K562	blood:	n/a	chr3:47942971-47942982
46	CEBPB	chr3:48003759-48004013	K562	blood:	n/a	n/a
47	CEBPB	chr3:48006243-48006691	HepG2	liver:	n/a	chr3:48006478-48006489
48	CEBPB	chr3:47931844-47932195	K562	blood:	n/a	chr3:47932017-47932028 chr3:47932018-47932027 chr3:47932016-47932027
49	CEBPB	chr3:47952212-47952595	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr3:47979888-47979957	H1-hESC	embryonic stem cell:	n/a	chr3:47979919-47979930

(count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:47893945-47893995	PANC-1	pancreas:	n/a
2	chr3:47952841-47952891	AG09319	gingival:	n/a
3	chr3:47893945-47893995	PANC-1	pancreas:	n/a
4	chr3:47952841-47952891	AG09319	gingival:	n/a
5	chr3:47893945-47893995	Jurkat	blood:	n/a
6	chr3:47952509-47952559	Hepatocyte	liver:	n/a
7	chr3:48004832-48004882	HRE	kidney:	n/a
8	chr3:47952841-47952891	SKMC	muscle:	n/a
9	chr3:47893945-47893995	K562	blood:	n/a
10	chr3:47952509-47952559	H1-hESC	embryonic stem cell:	embryo
11	chr3:47950807-47950857	HIPEpiC	eye:	n/a
12	chr3:48004832-48004882	AG10803	skin:	n/a
13	chr3:47950807-47950857	NH-A	brain:	n/a
14	chr3:48004832-48004882	HEK293	kidney:	embryo
15	chr3:47933600-47933650	HL-60	blood:	n/a
16	chr3:48004832-48004882	PFSK-1	brain:	n/a
17	chr3:47950807-47950857	SAEC	small airway:	n/a
18	chr3:47892279-47892329	HRE	kidney:	n/a
19	chr3:47952841-47952891	NHBE	bronchial:	n/a
20	chr3:47952611-47952661	HCF	heart:	n/a
21	chr3:47952841-47952891	Hela-S3	cervix:	n/a
22	chr3:48016946-48016996	HNPCEpiC	eye:	n/a
23	chr3:47952841-47952891	MCF10A-Er-Src	breast:	n/a
24	chr3:47952509-47952559	GM12891	blood:	n/a
25	chr3:47952509-47952559	HRPEpiC	eye:	n/a
26	chr3:47950807-47950857	MCF10A-Er-Src	breast:	n/a
27	chr3:47952509-47952559	BE2_C	brain:	n/a
28	chr3:47952098-47952148	AG10803	skin:	n/a
29	chr3:47952509-47952559	AoSMC	blood vessel:	n/a
30	chr3:47893945-47893995	HCM	heart:	n/a
31	chr3:47952611-47952661	Hepatocyte	liver:	n/a
32	chr3:47892279-47892329	GM12891	blood:	n/a
33	chr3:48004832-48004882	HIPEpiC	eye:	n/a
34	chr3:47950807-47950857	Caco-2	colon:	n/a
35	chr3:47932918-47932968	HCT-116	colon:	n/a
36	chr3:48004832-48004882	HCM	heart:	n/a
37	chr3:48018675-48018725	HRPEpiC	eye:	n/a
38	chr3:47952611-47952661	GM19239	blood:	n/a
39	chr3:48016946-48016996	LNCaP	prostate:	n/a
40	chr3:47933600-47933650	AG09309	skin:	n/a
41	chr3:48016946-48016996	HEK293	kidney:	embryo
42	chr3:47932918-47932968	AG10803	skin:	n/a
43	chr3:48016946-48016996	HL-60	blood:	n/a
44	chr3:47952611-47952661	HL-60	blood:	n/a
45	chr3:47952611-47952661	HCPEpiC	choroid plexus:	n/a
46	chr3:47950807-47950857	AG04449	skin:	fetal
47	chr3:47952841-47952891	CMK	blood:	n/a
48	chr3:47952509-47952559	SKMC	muscle:	n/a
49	chr3:47952098-47952148	AG09319	gingival:	n/a
50	chr3:47952611-47952661	IMR90	lung:	fetal

(count:66 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:47959598..47961533-chr3:47965469..47967262,2	K562	blood:
2	chr3:47891368..47892453-chr3:48031167..48032088,3	K562	blood:
3	chr3:47941256..47942794-chr3:47951029..47952546,2	MCF-7	breast:
4	chr3:47988815..47991729-chr3:47994715..47997497,2	K562	blood:
5	chr3:47954841..47956498-chr3:47961686..47964207,2	K562	blood:
6	chr3:47988815..47991729-chr3:47994715..47997497,2	K562	blood:
7	chr3:47919145..47920888-chr3:47933987..47935579,2	K562	blood:
8	chr3:47908132..47910392-chr3:47951934..47954399,2	K562	blood:
9	chr3:47995817..47998198-chr3:48000439..48002140,2	K562	blood:
10	chr3:47865886..47868261-chr3:47892861..47895381,3	K562	blood:
11	chr3:47976597..47979542-chr3:47982798..47984829,3	K562	blood:
12	chr3:47988815..47992482-chr3:47994715..47997497,3	K562	blood:
13	chr3:47893361..47897321-chr3:47899658..47903190,4	K562	blood:
14	chr3:47931648..47933684-chr3:47942643..47945311,2	K562	blood:
15	chr3:47940250..47943002-chr3:47945060..47946714,2	K562	blood:
16	chr3:47970944..47972483-chr3:47977512..47980509,2	K562	blood:
17	chr3:47877782..47879462-chr3:47906492..47908037,2	K562	blood:
18	chr3:47915163..47917361-chr3:47919966..47922770,2	K562	blood:
19	chr3:47893361..47897321-chr3:47899658..47903190,4	K562	blood:
20	chr3:47988815..47992482-chr3:47994715..47997497,3	K562	blood:
21	chr3:47867869..47870552-chr3:47891035..47892717,2	K562	blood:
22	chr3:47898431..47902857-chr3:47908612..47913870,6	K562	blood:
23	chr3:47865438..47868063-chr3:47949472..47951050,2	K562	blood:
24	chr3:47910657..47912296-chr3:48148741..48150868,2	K562	blood:
25	chr3:47930805..47933794-chr3:47935046..47936999,2	K562	blood:
26	chr3:47961751..47964593-chr3:47965535..47967248,2	K562	blood:
27	chr3:47948658..47950260-chr3:47950870..47952844,2	K562	blood:
28	chr12:94728960..94729681-chr3:48014076..48014912,2	MCF-7	breast:
29	chr3:47908495..47911109-chr3:47911186..47914669,4	K562	blood:
30	chr3:47919145..47920888-chr3:47933987..47935579,2	K562	blood:
31	chr3:48013205..48014837-chr3:48015200..48018193,2	MCF-7	breast:
32	chr3:47977230..47979542-chr3:47982942..47984829,2	K562	blood:
33	chr3:47952765..47954649-chr3:47957193..47959819,2	K562	blood:
34	chr3:47965405..47966999-chr3:47969364..47970935,2	K562	blood:
35	chr3:47952765..47954649-chr3:47957193..47959819,2	K562	blood:
36	chr3:47940568..47943002-chr3:47944240..47946560,3	K562	blood:
37	chr3:47881404..47884302-chr3:47904180..47905829,2	K562	blood:
38	chr3:48013205..48014837-chr3:48015200..48018193,2	MCF-7	breast:
39	chr3:47947689..47949234-chr3:47950366..47953123,2	K562	blood:
40	chr3:47880564..47882785-chr3:47892388..47894991,2	K562	blood:
41	chr3:47995817..47998198-chr3:48000439..48002140,2	K562	blood:
42	chr3:47895316..47897321-chr3:47900052..47901819,3	K562	blood:
43	chr3:47976597..47979542-chr3:47982798..47984829,3	K562	blood:
44	chr3:47912898..47916471-chr3:47916920..47919388,4	K562	blood:
45	chr3:47915163..47917361-chr3:47919966..47922770,2	K562	blood:
46	chr3:47895316..47897321-chr3:47900052..47901819,3	K562	blood:
47	chr3:47899451..47902057-chr3:48195294..48197379,2	K562	blood:
48	chr3:47908132..47910392-chr3:47951934..47954399,2	K562	blood:
49	chr3:47935127..47936630-chr3:47951043..47952545,2	K562	blood:
50	chr3:47928304..47929977-chr3:47930679..47933276,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SMARCC1-3	chr3:47912738-47912776	NONHSAT089533
2	lnc-SMARCC1-3	chr3:47913407-47913590	NONHSAT089533
3	lnc-SMARCC1-3	chr3:47918907-47919255	NONHSAT089533
4	lnc-SMARCC1-4	chr3:48001817-48002571	NONHSAT089536

No data

(count:12 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	MAP4	hsa-miR-328-3p	chr3:47893370-47893392
2	MAP4	hsa-miR-339-5p	chr3:48015903-48015924
3	MAP4	hsa-miR-103a-3p	chr3:47893478-47893499
4	MAP4	hsa-miR-16-5p	chr3:47893483-47893477
5	MAP4	hsa-miR-103a-3p	chr3:47893484-47893478
6	MAP4	hsa-miR-16-5p	chr3:47893477-47893498
7	MAP4	hsa-miR-92a-3p	chr3:48016702-48016724
8	MAP4	hsa-miR-23b-3p	chr3:48014618-48014638
9	MAP4	hsa-miR-328-3p	chr3:48016269-48016290
10	MAP4	hsa-miR-103a-3p	chr3:48016925-48016919
11	MAP4	hsa-miR-23b-3p	chr3:48014624-48014618
12	MAP4	hsa-miR-23b-3p	chr3:48014798-48014818

Variant related genes	Relation type
VPS26BP1	TF binding region
MAP4	TF binding region
ENSG00000199591	TF binding region
VPS26BP1	CpG island
MAP4	CpG island
ENSG00000199591	CpG island
ENSG00000173588	chromatin interactions
ENSG00000047849	chromatin interactions
ENSG00000132153	chromatin interactions

Extended variants
information (count: 4425 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:4425 , 50 per page) page: 1 2 3 4 5 6 7 ... 89

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531371500	chr3:47891716-47891717	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs549489595	chr3:47891736-47891737	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs200000824	chr3:47891743-47891744	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs10537180	chr3:47891745-47891746	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs397780895	chr3:47891746-47891747	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs537416935	chr3:47891753-47891754	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs372019061	chr3:47891757-47891758	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs571208978	chr3:47891780-47891781	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs545579205	chr3:47891802-47891803	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs538639197	chr3:47891805-47891806	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs547119118	chr3:47891828-47891829	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs565668650	chr3:47891832-47891833	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs562331106	chr3:47891839-47891840	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs536973067	chr3:47891840-47891841	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs2307872	chr3:47891863-47891864	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs116811344	chr3:47891928-47891929	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs576725366	chr3:47891934-47891935	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs571453230	chr3:47891944-47891945	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs144515390	chr3:47891974-47891975	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs559095100	chr3:47891976-47891977	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs545305001	chr3:47891981-47891982	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs529981439	chr3:47891991-47891992	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs577224521	chr3:47892041-47892042	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs79802831	chr3:47892062-47892063	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs559533478	chr3:47892067-47892068	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs531117037	chr3:47892084-47892085	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs371913961	chr3:47892114-47892115	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs117894418	chr3:47892122-47892123	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs560824770	chr3:47892147-47892148	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs531408303	chr3:47892152-47892153	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs201608720	chr3:47892164-47892165	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs2307874	chr3:47892165-47892166	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs386396576	chr3:47892166-47892167	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs560965853	chr3:47892171-47892172	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs549524443	chr3:47892175-47892176	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs565080747	chr3:47892177-47892178	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs78817662	chr3:47892183-47892184	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs547448455	chr3:47892184-47892185	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs111933914	chr3:47892188-47892189	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs567264648	chr3:47892231-47892232	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs1061138	chr3:47892236-47892237	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs536217981	chr3:47892279-47892280	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs548921197	chr3:47892315-47892316	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs1061112	chr3:47892338-47892339	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs375167512	chr3:47892344-47892345	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs141642911	chr3:47892345-47892346	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs186403729	chr3:47892351-47892352	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs191259255	chr3:47892355-47892356	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs369522695	chr3:47892364-47892365	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs571019979	chr3:47892373-47892374	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:100)

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
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	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
Melanoma	17363583	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Lung adenocarcinoma	21935476	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
abnormal development	18461090	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:3433 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:47867800-47899200	Strong transcription	Fetal Brain Female	brain
2	chr3:47867800-47918800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr3:47868000-47903000	Strong transcription	Cortex derived primary cultured neurospheres	brain
4	chr3:47868000-47915200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr3:47868200-47892200	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr3:47868200-47902400	Strong transcription	Monocytes-CD14+_RO01746	blood
7	chr3:47868400-47899200	Strong transcription	Rectal Mucosa Donor 31	rectum
8	chr3:47868400-47901200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
9	chr3:47868400-47902400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr3:47868400-47903000	Strong transcription	Placenta	Placenta
11	chr3:47868400-47903400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr3:47868400-47903400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr3:47868400-47916400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr3:47868400-47919000	Strong transcription	Fetal Stomach	stomach
15	chr3:47868600-47893600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr3:47868600-47899000	Strong transcription	Thymus	Thymus
17	chr3:47868600-47899200	Strong transcription	Primary monocytes fromperipheralblood	blood
18	chr3:47868600-47899200	Strong transcription	Primary T cells from cord blood	blood
19	chr3:47868600-47899400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
20	chr3:47868600-47901800	Strong transcription	Fetal Intestine Large	intestine
21	chr3:47868600-47902200	Strong transcription	Primary T cells fromperipheralblood	blood
22	chr3:47868600-47902600	Strong transcription	Liver	Liver
23	chr3:47868600-47902800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
24	chr3:47868600-47912200	Strong transcription	Fetal Intestine Small	intestine
25	chr3:47868800-47894000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
26	chr3:47868800-47902000	Strong transcription	Duodenum Smooth Muscle	Duodenum
27	chr3:47868800-47902200	Strong transcription	Duodenum Mucosa	Duodenum
28	chr3:47868800-47902400	Strong transcription	Osteobl	bone
29	chr3:47869000-47897400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr3:47869000-47897400	Strong transcription	Adipose Nuclei	Adipose
31	chr3:47869000-47897800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr3:47869000-47899400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
33	chr3:47869000-47902400	Strong transcription	Sigmoid Colon	Sigmoid Colon
34	chr3:47869000-47918600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr3:47869200-47902200	Strong transcription	Dnd41	blood
36	chr3:47870800-47931800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
37	chr3:47871200-47899200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
38	chr3:47871400-47892600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr3:47871400-47899200	Strong transcription	Fetal Thymus	thymus
40	chr3:47871600-47892000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr3:47871600-47894200	Strong transcription	Primary T helper cells PMA-I stimulated	--
42	chr3:47871600-47899200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
43	chr3:47871800-47899200	Strong transcription	Gastric	stomach
44	chr3:47871800-47901600	Strong transcription	Brain Germinal Matrix	brain
45	chr3:47872000-47899400	Strong transcription	Primary T helper cells fromperipheralblood	blood
46	chr3:47872200-47899200	Strong transcription	Muscle Satellite Cultured Cells	--
47	chr3:47875800-47893200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
48	chr3:47876000-47899000	Strong transcription	Rectal Smooth Muscle	rectum
49	chr3:47877200-47892400	Strong transcription	Primary neutrophils fromperipheralblood	blood
50	chr3:47877200-47895800	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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