Variant report

Variant	nsv984575
Chromosome Location	chr5:179759624-179791220
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:468)
CpG islands
(count:1708)
Chromatin interactive
region (count:33)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:468 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr5:179770369-179771163	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr5:179781289-179781456	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr5:179779932-179780969	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr5:179779057-179779111	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr5:179770098-179770954	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr5:179779393-179779698	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL3	chr5:179760458-179761065	A549	lung:	n/a	n/a
8	BCL3	chr5:179760561-179761070	A549	lung:	n/a	n/a
9	BRCA1	chr5:179770456-179770896	H1-hESC	embryonic stem cell:	n/a	n/a
10	CCNT2	chr5:179779882-179780557	K562	blood:	n/a	n/a
11	CEBPB	chr5:179780557-179780688	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr5:179760604-179761012	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr5:179760526-179761150	A549	lung:	n/a	n/a
14	CEBPB	chr5:179770101-179770540	IMR90	lung:	n/a	n/a
15	CEBPB	chr5:179771031-179771432	A549	lung:	n/a	n/a
16	CEBPB	chr5:179769172-179769351	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr5:179770939-179771507	HCT-116	colon:	n/a	n/a
18	CEBPB	chr5:179770974-179771480	ECC-1	luminal epithelium:	n/a	n/a
19	CEBPB	chr5:179765096-179765231	IMR90	lung:	n/a	n/a
20	CEBPB	chr5:179771065-179771395	K562	blood:	n/a	n/a
21	CEBPB	chr5:179770955-179771594	MCF-7	breast:	n/a	n/a
22	CEBPB	chr5:179769310-179769411	K562	blood:	n/a	n/a
23	CEBPB	chr5:179769285-179769422	IMR90	lung:	n/a	n/a
24	CEBPB	chr5:179771037-179771330	K562	blood:	n/a	n/a
25	CEBPB	chr5:179770938-179771520	MCF-7	breast:	n/a	n/a
26	CEBPB	chr5:179770928-179771445	A549	lung:	n/a	n/a
27	CEBPB	chr5:179771014-179771362	ECC-1	luminal epithelium:	n/a	n/a
28	CEBPB	chr5:179771121-179771355	HepG2	liver:	n/a	n/a
29	CEBPB	chr5:179770913-179771487	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr5:179760595-179761042	A549	lung:	n/a	n/a
31	CEBPB	chr5:179771027-179771408	IMR90	lung:	n/a	n/a
32	CEBPB	chr5:179781371-179781794	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr5:179785778-179785968	HepG2	liver:	n/a	chr5:179785901-179785912
34	CEBPB	chr5:179770776-179771561	A549	lung:	n/a	n/a
35	CEBPB	chr5:179770658-179771403	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD1	chr5:179781283-179781444	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD1	chr5:179778983-179779395	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD1	chr5:179770374-179770560	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr5:179779555-179779587	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr5:179771103-179771384	Hela-S3	cervix:	n/a	n/a
41	CHD2	chr5:179779522-179779523	Hela-S3	cervix:	n/a	n/a
42	CHD2	chr5:179770065-179770867	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD2	chr5:179780541-179780552	K562	blood:	n/a	n/a
44	CHD2	chr5:179774667-179774886	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr5:179760666-179761051	Hela-S3	cervix:	n/a	n/a
46	CHD2	chr5:179780278-179780586	Hela-S3	cervix:	n/a	n/a
47	CHD2	chr5:179768916-179769167	K562	blood:	n/a	n/a
48	CHD2	chr5:179780289-179780553	H1-hESC	embryonic stem cell:	n/a	n/a
49	CREB1	chr5:179769895-179770738	H1-hESC	embryonic stem cell:	n/a	n/a
50	CREB1	chr5:179760667-179761016	A549	lung:	n/a	n/a

(count:1708 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:179763951-179764001	Jurkat	blood:	n/a
2	chr5:179763494-179763544	HCM	heart:	n/a
3	chr5:179762999-179763049	NB4	blood:	n/a
4	chr5:179775488-179775538	AG04450	lung:	fetal
5	chr5:179778527-179778577	HIPEpiC	eye:	n/a
6	chr5:179781547-179781597	HL-60	blood:	n/a
7	chr5:179765497-179765547	HRCEpiC	kidney:	n/a
8	chr5:179780409-179780459	GM12878	blood:	n/a
9	chr5:179765497-179765547	NHBE	bronchial:	n/a
10	chr5:179763951-179764001	MCF-7	breast:	n/a
11	chr5:179765449-179765499	MCF-7	breast:	n/a
12	chr5:179763055-179763105	GM12892	blood:	n/a
13	chr5:179770299-179770349	GM12892	blood:	n/a
14	chr5:179779205-179779255	AG09309	skin:	n/a
15	chr5:179780314-179780364	SAEC	small airway:	n/a
16	chr5:179763494-179763544	MCF-7	breast:	n/a
17	chr5:179783846-179783896	GM12892	blood:	n/a
18	chr5:179779237-179779287	HRCEpiC	kidney:	n/a
19	chr5:179763055-179763105	RPTEC	kidney:	n/a
20	chr5:179779237-179779287	HNPCEpiC	eye:	n/a
21	chr5:179778527-179778577	U87	brain:	n/a
22	chr5:179779115-179779165	GM12892	blood:	n/a
23	chr5:179781245-179781295	LNCaP	prostate:	n/a
24	chr5:179771628-179771678	T-47D	breast:	n/a
25	chr5:179770299-179770349	Jurkat	blood:	n/a
26	chr5:179780409-179780459	MCF10A-Er-Src	breast:	n/a
27	chr5:179763678-179763728	U87	brain:	n/a
28	chr5:179781245-179781295	BJ	skin:	n/a
29	chr5:179770299-179770349	SK-N-MC	brain:	n/a
30	chr5:179781245-179781295	GM12891	blood:	n/a
31	chr5:179763055-179763105	NH-A	brain:	n/a
32	chr5:179779123-179779173	T-47D	breast:	n/a
33	chr5:179779123-179779173	Hela-S3	cervix:	n/a
34	chr5:179779237-179779287	SK-N-SH	brain:	n/a
35	chr5:179783846-179783896	LNCaP	prostate:	n/a
36	chr5:179765449-179765499	AG09309	skin:	n/a
37	chr5:179780409-179780459	AG04450	lung:	fetal
38	chr5:179780563-179780613	U87	brain:	n/a
39	chr5:179779664-179779714	Hepatocyte	liver:	n/a
40	chr5:179765449-179765499	SK-N-SH_RA	brain:	n/a
41	chr5:179771628-179771678	ProgFib	skin:	n/a
42	chr5:179775488-179775538	GM12878	blood:	n/a
43	chr5:179777565-179777615	A549	lung:	n/a
44	chr5:179780802-179780852	HNPCEpiC	eye:	n/a
45	chr5:179779115-179779165	ovcar-3	ovarian:	n/a
46	chr5:179779664-179779714	H1-hESC	embryonic stem cell:	embryo
47	chr5:179780563-179780613	HRCEpiC	kidney:	n/a
48	chr5:179775488-179775538	ProgFib	skin:	n/a
49	chr5:179763494-179763544	T-47D	breast:	n/a
50	chr5:179762999-179763049	ovcar-3	ovarian:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:179780821..179782818-chr5:179787317..179788997,2	K562	blood:
2	chr5:179714950..179716889-chr5:179783751..179785977,2	K562	blood:
3	chr5:179743533..179745138-chr5:179758966..179761002,2	K562	blood:
4	chr5:179717698..179720150-chr5:179758033..179760822,3	MCF-7	breast:
5	chr5:179763941..179765836-chr5:179767390..179770088,2	K562	blood:
6	chr5:179778332..179781251-chr5:179920436..179923318,3	MCF-7	breast:
7	chr5:179767711..179769306-chr5:179771543..179774256,2	K562	blood:
8	chr5:179767711..179769306-chr5:179771543..179774256,2	K562	blood:
9	chr5:179758118..179760214-chr5:179779421..179781494,2	MCF-7	breast:
10	chr5:179758118..179760214-chr5:179779421..179781494,2	MCF-7	breast:
11	chr5:179771513..179773168-chr5:179773913..179776480,2	K562	blood:
12	chr5:179758082..179759697-chr5:179760362..179762379,2	MCF-7	breast:
13	chr5:179779053..179781743-chr5:179782103..179785187,4	MCF-7	breast:
14	chr5:179761366..179762907-chr5:179778536..179780759,2	MCF-7	breast:
15	chr5:179772488..179776798-chr5:179777928..179781659,4	K562	blood:
16	chr5:179776807..179778775-chr5:179896611..179898165,2	MCF-7	breast:
17	chr5:179739354..179741668-chr5:179785404..179788387,2	MCF-7	breast:
18	chr5:179755365..179757615-chr5:179761406..179763311,3	K562	blood:
19	chr5:179763941..179765836-chr5:179767390..179770088,2	K562	blood:
20	chr5:179775628..179778352-chr5:179778745..179780762,2	MCF-7	breast:
21	chr5:179761126..179762815-chr5:179764028..179766885,2	MCF-7	breast:
22	chr5:179760436..179761974-chr5:179802802..179805254,2	MCF-7	breast:
23	chr5:179780821..179782818-chr5:179787317..179788997,2	K562	blood:
24	chr5:179770572..179772662-chr5:179890635..179892698,2	MCF-7	breast:
25	chr5:179761126..179762815-chr5:179764028..179766885,2	MCF-7	breast:
26	chr5:179771513..179773168-chr5:179773913..179776480,2	K562	blood:
27	chr5:179771173..179772905-chr5:179777611..179780559,4	MCF-7	breast:
28	chr5:179769960..179774834-chr5:179776858..179780892,7	MCF-7	breast:
29	chr5:179762875..179766753-chr5:179777618..179780359,3	MCF-7	breast:
30	chr5:179761022..179762666-chr5:179778358..179780120,2	MCF-7	breast:
31	chr5:179773523..179775138-chr5:179800257..179803108,2	MCF-7	breast:
32	chr5:179720130..179723028-chr5:179758867..179761631,2	MCF-7	breast:
33	chr5:179769448..179771276-chr5:179896602..179898870,2	MCF-7	breast:

No data

Variant related genes	Relation type
GFPT2	TF binding region
GFPT2	CpG island
ENSG00000248367	chromatin interactions
ENSG00000113300	chromatin interactions
ENSG00000050748	chromatin interactions
ENSG00000131459	chromatin interactions

Extended variants
information (count: 1400 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:1400 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564160597	chr5:179759633-179759634	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs532906359	chr5:179759640-179759641	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs549912293	chr5:179759687-179759688	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs138816256	chr5:179759698-179759699	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs571956635	chr5:179759713-179759714	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs548856039	chr5:179759714-179759715	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs565647394	chr5:179759719-179759720	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs141957304	chr5:179759721-179759722	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs557891134	chr5:179759756-179759757	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs550058217	chr5:179759759-179759760	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs569503436	chr5:179759760-179759761	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs189043314	chr5:179759778-179759779	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs144862010	chr5:179759810-179759811	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs374765769	chr5:179759842-179759843	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs543281806	chr5:179759860-179759861	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs553660242	chr5:179759868-179759869	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs181388509	chr5:179759881-179759882	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs548632625	chr5:179759882-179759883	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs185610707	chr5:179759883-179759884	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs6601110	chr5:179759928-179759929	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs7727934	chr5:179760013-179760014	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs188558250	chr5:179760026-179760027	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs557215905	chr5:179760032-179760033	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs563083745	chr5:179760046-179760047	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs77652970	chr5:179760120-179760121	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs72811044	chr5:179760129-179760130	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs565609104	chr5:179760184-179760185	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs78205735	chr5:179760208-179760209	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs528383762	chr5:179760237-179760238	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs11341578	chr5:179760240-179760241	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs180958814	chr5:179760274-179760275	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs557658423	chr5:179760295-179760296	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs571526095	chr5:179760296-179760297	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs142938952	chr5:179760298-179760299	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs573918614	chr5:179760352-179760353	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs557168004	chr5:179760360-179760361	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs543078745	chr5:179760373-179760374	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs536798614	chr5:179760391-179760392	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs369897273	chr5:179760398-179760399	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs553483498	chr5:179760424-179760425	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs573421747	chr5:179760435-179760436	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs541218850	chr5:179760436-179760437	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs564085139	chr5:179760463-179760464	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs573544431	chr5:179760476-179760477	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs185781189	chr5:179760477-179760478	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs58553716	chr5:179760481-179760482	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs577562482	chr5:179760492-179760493	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs543414756	chr5:179760514-179760515	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs6874176	chr5:179760525-179760526	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs367679503	chr5:179760549-179760550	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	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
Prostate cancer	18632612	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Autism	20808228	CNVD
small cell lung cancer	20016488	CNVD
Autism	22543975	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1266 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:179728600-179761400	Weak transcription	Aorta	Aorta
2	chr5:179739600-179761200	Weak transcription	Duodenum Smooth Muscle	Duodenum
3	chr5:179741600-179762600	Weak transcription	Rectal Smooth Muscle	rectum
4	chr5:179743200-179761000	Weak transcription	Right Ventricle	heart
5	chr5:179744000-179766600	Weak transcription	Gastric	stomach
6	chr5:179746000-179760800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr5:179746000-179761400	Weak transcription	Right Atrium	heart
8	chr5:179752400-179760800	Weak transcription	Brain Germinal Matrix	brain
9	chr5:179752400-179760800	Weak transcription	Brain Substantia Nigra	brain
10	chr5:179755000-179759800	Enhancers	Placenta	Placenta
11	chr5:179755800-179760800	Weak transcription	Lung	lung
12	chr5:179756000-179760800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr5:179756200-179761000	Weak transcription	Brain Hippocampus Middle	brain
14	chr5:179756200-179761600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr5:179756400-179760600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr5:179757000-179761000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr5:179757000-179779000	Weak transcription	Esophagus	oesophagus
18	chr5:179757200-179761000	Weak transcription	Fetal Brain Female	brain
19	chr5:179757400-179759800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr5:179757800-179760600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
21	chr5:179757800-179765600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr5:179758000-179761000	Weak transcription	Brain Angular Gyrus	brain
23	chr5:179758200-179760400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr5:179758200-179760600	Weak transcription	Brain Inferior Temporal Lobe	brain
25	chr5:179758400-179760800	Enhancers	Muscle Satellite Cultured Cells	--
26	chr5:179758600-179761000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr5:179758600-179761400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
28	chr5:179758800-179760000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr5:179758800-179760800	Weak transcription	Brain Cingulate Gyrus	brain
30	chr5:179758800-179761000	Weak transcription	Skeletal Muscle Female	skeletal muscle
31	chr5:179759000-179759800	Weak transcription	HSMM	muscle
32	chr5:179759000-179760000	Weak transcription	H9 Cell Line	embryonic stem cell
33	chr5:179759000-179760400	Weak transcription	NHDF-Ad	bronchial
34	chr5:179759000-179760600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr5:179759000-179760600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
36	chr5:179759000-179760600	Weak transcription	Adipose Nuclei	Adipose
37	chr5:179759000-179760600	Weak transcription	Brain Anterior Caudate	brain
38	chr5:179759000-179760600	Weak transcription	Fetal Muscle Leg	muscle
39	chr5:179759000-179760600	Weak transcription	Placenta Amnion	Placenta Amnion
40	chr5:179759000-179760600	Enhancers	Hela-S3	cervix
41	chr5:179759000-179760800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr5:179759000-179760800	Weak transcription	Stomach Smooth Muscle	stomach
43	chr5:179759000-179760800	Enhancers	A549	lung
44	chr5:179759000-179760800	Weak transcription	HSMMtube	muscle
45	chr5:179759000-179760800	Weak transcription	NHLF	lung
46	chr5:179759000-179761000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr5:179759000-179761000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr5:179759000-179761000	Enhancers	NH-A	brain
49	chr5:179759000-179761400	Weak transcription	Fetal Lung	lung
50	chr5:179759000-179762800	Weak transcription	Pancreas	Pancrea

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