Variant report

Variant	nsv1040539
Chromosome Location	chr9:71600042-71844108
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:5830)
CpG islands
(count:2992)
Chromatin interactive
region (count:253)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:5830 , 50 per page) page: 1 2 3 4 5 6 7 ... 117

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:71783969-71784100	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:71701730-71702036	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:71788981-71788988	K562	blood:	n/a	n/a
4	ARID3A	chr9:71719221-71720293	HepG2	liver:	n/a	chr9:71719768-71719784 chr9:71719315-71719331
5	ARID3A	chr9:71830850-71831360	K562	blood:	n/a	n/a
6	ARID3A	chr9:71819420-71819690	K562	blood:	n/a	n/a
7	ARID3A	chr9:71795418-71795995	HepG2	liver:	n/a	n/a
8	ARID3A	chr9:71735292-71735927	HepG2	liver:	n/a	n/a
9	ARID3A	chr9:71642563-71642873	K562	blood:	n/a	n/a
10	ARID3A	chr9:71614594-71614886	HepG2	liver:	n/a	n/a
11	ARID3A	chr9:71635426-71635919	K562	blood:	n/a	n/a
12	ARID3A	chr9:71803674-71804222	K562	blood:	n/a	n/a
13	ARID3A	chr9:71822394-71822631	K562	blood:	n/a	n/a
14	ARID3A	chr9:71787032-71787270	HepG2	liver:	n/a	n/a
15	ARID3A	chr9:71746529-71747015	HepG2	liver:	n/a	n/a
16	ARID3A	chr9:71651502-71651839	K562	blood:	n/a	n/a
17	ARID3A	chr9:71631852-71631872	K562	blood:	n/a	n/a
18	ARID3A	chr9:71821041-71821305	K562	blood:	n/a	n/a
19	ARID3A	chr9:71808137-71808737	K562	blood:	n/a	n/a
20	ARID3A	chr9:71800451-71800521	K562	blood:	n/a	n/a
21	ARID3A	chr9:71634748-71635103	K562	blood:	n/a	n/a
22	ARID3A	chr9:71785228-71785657	K562	blood:	n/a	n/a
23	ARID3A	chr9:71793431-71794296	HepG2	liver:	n/a	n/a
24	ARID3A	chr9:71805069-71805695	HepG2	liver:	n/a	chr9:71805429-71805445 chr9:71805430-71805446
25	ARID3A	chr9:71785862-71786328	K562	blood:	n/a	n/a
26	ARID3A	chr9:71802085-71802622	K562	blood:	n/a	n/a
27	ARID3A	chr9:71801110-71801635	HepG2	liver:	n/a	n/a
28	ARID3A	chr9:71820008-71820023	K562	blood:	n/a	n/a
29	ARID3A	chr9:71650526-71650743	K562	blood:	n/a	n/a
30	ARID3A	chr9:71650444-71651128	HepG2	liver:	n/a	n/a
31	ARID3A	chr9:71768528-71769284	HepG2	liver:	n/a	n/a
32	ARID3A	chr9:71795383-71796025	K562	blood:	n/a	n/a
33	ARID3A	chr9:71808074-71808402	HepG2	liver:	n/a	n/a
34	ARID3A	chr9:71801237-71801527	K562	blood:	n/a	n/a
35	ATF1	chr9:71802159-71802633	K562	blood:	n/a	n/a
36	ATF1	chr9:71635543-71635967	K562	blood:	n/a	n/a
37	ATF1	chr9:71785927-71786382	K562	blood:	n/a	n/a
38	ATF1	chr9:71795567-71795986	K562	blood:	n/a	n/a
39	ATF1	chr9:71634756-71635094	K562	blood:	n/a	n/a
40	ATF1	chr9:71613777-71614153	K562	blood:	n/a	n/a
41	ATF1	chr9:71803941-71804270	K562	blood:	n/a	n/a
42	ATF1	chr9:71830870-71831226	K562	blood:	n/a	n/a
43	ATF1	chr9:71642591-71642873	K562	blood:	n/a	n/a
44	ATF2	chr9:71737566-71738148	H1-hESC	embryonic stem cell:	n/a	n/a
45	ATF2	chr9:71838407-71838832	H1-hESC	embryonic stem cell:	n/a	n/a
46	ATF2	chr9:71789602-71790821	GM12878	blood:	n/a	n/a
47	ATF2	chr9:71737258-71738069	H1-hESC	embryonic stem cell:	n/a	n/a
48	ATF2	chr9:71650325-71650801	H1-hESC	embryonic stem cell:	n/a	n/a
49	ATF2	chr9:71783777-71784242	GM12878	blood:	n/a	n/a
50	ATF2	chr9:71735106-71735934	H1-hESC	embryonic stem cell:	n/a	n/a

(count:2992 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:71737204-71737254	SK-N-SH	brain:	n/a
2	chr9:71787160-71787210	Hepatocyte	liver:	n/a
3	chr9:71834813-71834863	HRPEpiC	eye:	n/a
4	chr9:71737204-71737254	SK-N-SH	brain:	n/a
5	chr9:71787160-71787210	Hepatocyte	liver:	n/a
6	chr9:71834813-71834863	HRPEpiC	eye:	n/a
7	chr9:71735666-71735716	HCT-116	colon:	n/a
8	chr9:71834813-71834863	CMK	blood:	n/a
9	chr9:71623401-71623451	Hela-S3	cervix:	n/a
10	chr9:71683936-71683986	CMK	blood:	n/a
11	chr9:71737258-71737308	HMEC	breast:	n/a
12	chr9:71787778-71787828	HNPCEpiC	eye:	n/a
13	chr9:71833386-71833436	PrEC	prostate:	n/a
14	chr9:71792936-71792986	ovcar-3	ovarian:	n/a
15	chr9:71682302-71682352	GM12878	blood:	n/a
16	chr9:71651175-71651225	HUVEC	blood vessel:	n/a
17	chr9:71833386-71833436	RPTEC	kidney:	n/a
18	chr9:71787778-71787828	GM19239	blood:	n/a
19	chr9:71732345-71732395	MCF10A-Er-Src	breast:	n/a
20	chr9:71792936-71792986	HCM	heart:	n/a
21	chr9:71628906-71628956	HRPEpiC	eye:	n/a
22	chr9:71787778-71787828	HUVEC	blood vessel:	n/a
23	chr9:71736409-71736459	AG09309	skin:	n/a
24	chr9:71669714-71669764	CMK	blood:	n/a
25	chr9:71623401-71623451	HCM	heart:	n/a
26	chr9:71837449-71837499	Caco-2	colon:	n/a
27	chr9:71736409-71736459	Hela-S3	cervix:	n/a
28	chr9:71736999-71737049	HRPEpiC	eye:	n/a
29	chr9:71682105-71682155	GM19239	blood:	n/a
30	chr9:71627524-71627574	GM12878	blood:	n/a
31	chr9:71792936-71792986	U87	brain:	n/a
32	chr9:71650719-71650769	HRE	kidney:	n/a
33	chr9:71837449-71837499	SK-N-SH_RA	brain:	n/a
34	chr9:71669714-71669764	Caco-2	colon:	n/a
35	chr9:71788759-71788809	PANC-1	pancreas:	n/a
36	chr9:71623401-71623451	NT2-D1	testis:	n/a
37	chr9:71837449-71837499	AG10803	skin:	n/a
38	chr9:71789541-71789591	NB4	blood:	n/a
39	chr9:71650719-71650769	HAEpiC	amniotic membrane:	n/a
40	chr9:71736854-71736904	HCF	heart:	n/a
41	chr9:71834813-71834863	HUVEC	blood vessel:	n/a
42	chr9:71623401-71623451	ProgFib	skin:	n/a
43	chr9:71788759-71788809	K562	blood:	n/a
44	chr9:71788759-71788809	HL-60	blood:	n/a
45	chr9:71623401-71623451	ovcar-3	ovarian:	n/a
46	chr9:71650719-71650769	AG10803	skin:	n/a
47	chr9:71647192-71647242	HEK293	kidney:	embryo
48	chr9:71833386-71833436	SK-N-SH	brain:	n/a
49	chr9:71623401-71623451	AG09309	skin:	n/a
50	chr9:71785587-71785637	HCM	heart:	n/a

(count:253 , 50 per page) page: 1 2 3 4 5 6

No.	Distal block	Cell Line	Cell type
1	chr9:71745094..71746594-chr9:71762879..71765148,2	MCF-7	breast:
2	chr9:71730545..71732525-chr9:71797822..71800476,2	K562	blood:
3	chr9:71649801..71651906-chr9:71729690..71731454,2	MCF-7	breast:
4	chr9:71782411..71787293-chr9:71788939..71792215,6	K562	blood:
5	chr9:71651712..71654573-chr9:71656499..71659593,3	K562	blood:
6	chr9:71734142..71739001-chr9:71788032..71795507,11	MCF-7	breast:
7	chr9:71601422..71604412-chr9:71607352..71608900,2	MCF-7	breast:
8	chr9:71768851..71770406-chr9:71807672..71810117,2	MCF-7	breast:
9	chr9:71198223..71198730-chr9:71614318..71615145,2	MCF-7	breast:
10	chr9:71727081..71728601-chr9:71737166..71739059,2	MCF-7	breast:
11	chr9:71793727..71795446-chr9:71807376..71809123,2	MCF-7	breast:
12	chr9:71634711..71636591-chr9:71649540..71651584,2	MCF-7	breast:
13	chr9:71743905..71746446-chr9:71805495..71808231,2	MCF-7	breast:
14	chr9:71736348..71739276-chr9:71751743..71753516,2	MCF-7	breast:
15	chr9:71733168..71738729-chr9:71786929..71793777,10	MCF-7	breast:
16	chr9:71761121..71762822-chr9:71762920..71764542,2	K562	blood:
17	chr9:71793727..71795446-chr9:71807376..71809123,2	MCF-7	breast:
18	chr9:71680609..71683537-chr9:71732525..71735089,2	MCF-7	breast:
19	chr9:71798131..71799806-chr9:71811511..71814165,2	MCF-7	breast:
20	chr9:71650597..71652252-chr9:71824888..71827818,2	MCF-7	breast:
21	chr9:71779511..71782336-chr9:71782342..71784212,2	MCF-7	breast:
22	chr9:71789625..71792443-chr9:71836331..71838562,2	K562	blood:
23	chr9:71704008..71706268-chr9:71714594..71717470,2	MCF-7	breast:
24	chr9:71770660..71772249-chr9:71774354..71777333,2	MCF-7	breast:
25	chr9:71830235..71832170-chr9:71836510..71838640,2	K562	blood:
26	chr9:71671307..71672957-chr9:71675793..71678189,2	MCF-7	breast:
27	chr9:71699941..71701534-chr9:71703830..71705802,2	MCF-7	breast:
28	chr9:71842807..71845756-chr9:71852828..71854737,2	MCF-7	breast:
29	chr9:71634014..71636230-chr9:71638337..71641027,2	K562	blood:
30	chr9:71655862..71658846-chr9:71661896..71664645,2	MCF-7	breast:
31	chr9:71650420..71652084-chr9:71654261..71655791,2	MCF-7	breast:
32	chr9:71651891..71654666-chr9:71794283..71796361,2	MCF-7	breast:
33	chr9:71671307..71672957-chr9:71675793..71678189,2	MCF-7	breast:
34	chr9:71612570..71616113-chr9:71618356..71621633,3	K562	blood:
35	chr3:45017283..45018160-chr9:71735845..71736825,2	Hela-S3	cervix:
36	chr9:71736310..71738206-chr9:71797242..71798901,2	MCF-7	breast:
37	chr9:71743521..71745547-chr9:71821447..71823888,2	MCF-7	breast:
38	chr9:71726688..71731938-chr9:71734130..71739301,8	MCF-7	breast:
39	chr9:71732215..71735155-chr9:71735593..71737924,2	MCF-7	breast:
40	chr9:71735183..71737374-chr9:71783911..71785475,2	MCF-7	breast:
41	chr9:71743521..71745547-chr9:71821447..71823888,2	MCF-7	breast:
42	chr9:71649461..71652506-chr9:71658685..71662535,4	MCF-7	breast:
43	chr9:71814337..71816203-chr9:71818025..71821433,3	MCF-7	breast:
44	chr9:71640222..71642541-chr9:71649127..71652222,3	MCF-7	breast:
45	chr9:71704193..71706680-chr9:71707400..71709954,2	K562	blood:
46	chr9:71674276..71676864-chr9:71678272..71680734,2	MCF-7	breast:
47	chr13:48611578..48612294-chr9:71736012..71736825,2	Hela-S3	cervix:
48	chr9:71639276..71640998-chr9:71649555..71652246,2	MCF-7	breast:
49	chr9:71724269..71725816-chr9:71735725..71737678,2	MCF-7	breast:
50	chr9:71628740..71631389-chr9:71634679..71636239,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRKACG-2	chr9:71785572-71785971	ENSG00000250944
2	lnc-TJP2-1	chr9:71736209-71736281	ENSG00000227410.1
3	lnc-TJP2-1	chr9:71736400-71737148	ENSG00000227410.1
4	lnc-PRKACG-4	chr9:71624143-71625000	ucscGeneNc_uc004ahk_2
5	lnc-PRKACG-4	chr9:71625289-71625403	ucscGeneNc_uc004ahk_2
6	lnc-PRKACG-2	chr9:71780235-71782388	ENSG00000250944

No data

Variant related genes	Relation type
PRKACG	TF binding region
TJP2	TF binding region
FXN	TF binding region
ENSG00000270236	TF binding region
PRKACG	CpG island
TJP2	CpG island
FXN	CpG island
ENSG00000270236	CpG island
ENSG00000001167	chromatin interactions
ENSG00000136159	chromatin interactions
ENSG00000187866	chromatin interactions
ENSG00000136143	chromatin interactions
ENSG00000124222	chromatin interactions
ENSG00000135063	chromatin interactions
ENSG00000132849	chromatin interactions
ENSG00000254995	chromatin interactions
ENSG00000163812	chromatin interactions
ENSG00000165060	chromatin interactions
ENSG00000119139	chromatin interactions
ENSG00000272434	chromatin interactions
ENSG00000075914	chromatin interactions
ENSG00000270236	chromatin interactions
ENSG00000126216	chromatin interactions
ENSG00000178035	chromatin interactions
ENSG00000206737	chromatin interactions
ENSG00000165059	chromatin interactions
FLOT1	miRNA target sites
APITD1	miRNA target sites

Extended variants
information (count: 9478 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:9478 , 50 per page) page: 1 2 3 4 5 6 7 ... 190

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs578057945	chr9:71600062-71600063	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs545043043	chr9:71600070-71600071	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs560558410	chr9:71600083-71600084	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs201676082	chr9:71600163-71600164	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs368827344	chr9:71600170-71600171	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs143465449	chr9:71600261-71600262	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs188405792	chr9:71600262-71600263	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs561137351	chr9:71600325-71600326	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs147972691	chr9:71600368-71600369	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs532256250	chr9:71600397-71600398	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs549966097	chr9:71600405-71600406	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs181140859	chr9:71600406-71600407	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs532248101	chr9:71600468-71600469	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs28429307	chr9:71600472-71600473	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs565695605	chr9:71600534-71600535	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs185581421	chr9:71600593-71600594	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs189420870	chr9:71600614-71600615	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs117031146	chr9:71600762-71600763	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs537193752	chr9:71600775-71600776	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs558735165	chr9:71600787-71600788	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs4744771	chr9:71600814-71600815	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs536631754	chr9:71600822-71600823	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs545514116	chr9:71600869-71600870	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs150155134	chr9:71600950-71600951	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs376329797	chr9:71600967-71600968	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs180895557	chr9:71600970-71600971	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs542911530	chr9:71601005-71601006	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs568044798	chr9:71601022-71601023	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs561200513	chr9:71601080-71601081	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs531892700	chr9:71601100-71601101	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs543575255	chr9:71601117-71601118	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs187205429	chr9:71601136-71601137	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs372441984	chr9:71601141-71601142	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs532086097	chr9:71601158-71601159	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs7040120	chr9:71601171-71601172	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs570708635	chr9:71601188-71601189	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs114198740	chr9:71601190-71601191	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs10156412	chr9:71601237-71601238	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs553231810	chr9:71601262-71601263	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs192037407	chr9:71601282-71601283	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs138835877	chr9:71601303-71601304	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs573283221	chr9:71601360-71601361	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs558453830	chr9:71601377-71601378	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs142829476	chr9:71601379-71601380	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs201354126	chr9:71601385-71601386	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs554289020	chr9:71601403-71601404	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs12350193	chr9:71601408-71601409	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs542573405	chr9:71601430-71601431	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs200612959	chr9:71601438-71601439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs80170767	chr9:71601507-71601508	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	17899364	CNVD
Mantle cell lymphoma	19029149	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	20729466	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Oral cancer	21386901	CNVD
Epilepsy	22083797	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Bipolar disorder	18458673	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:7121 , 50 per page) page: 1 2 3 4 5 6 7 ... 143

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:71590800-71606400	Weak transcription	Stomach Mucosa	stomach
2	chr9:71593600-71606200	Weak transcription	Primary neutrophils fromperipheralblood	blood
3	chr9:71594800-71628400	Weak transcription	Spleen	Spleen
4	chr9:71595000-71600600	Weak transcription	Primary B cells from cord blood	blood
5	chr9:71595200-71606400	Weak transcription	Lung	lung
6	chr9:71595200-71628000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr9:71595200-71631600	Weak transcription	Gastric	stomach
8	chr9:71595400-71600400	Weak transcription	Duodenum Mucosa	Duodenum
9	chr9:71595800-71626200	Weak transcription	Colonic Mucosa	Colon
10	chr9:71596200-71612200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr9:71597000-71609200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr9:71597200-71600200	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr9:71597200-71605800	Weak transcription	Primary B cells from peripheral blood	blood
14	chr9:71597200-71606000	Weak transcription	Rectal Mucosa Donor 29	rectum
15	chr9:71597200-71613000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
16	chr9:71597200-71626000	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr9:71597400-71600200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr9:71597400-71611800	Weak transcription	Fetal Stomach	stomach
19	chr9:71598000-71601200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr9:71598400-71613200	Weak transcription	Right Ventricle	heart
21	chr9:71598600-71600200	Enhancers	Fetal Heart	heart
22	chr9:71598600-71601000	Strong transcription	Fetal Intestine Large	intestine
23	chr9:71598600-71605400	Weak transcription	Primary monocytes fromperipheralblood	blood
24	chr9:71598600-71606200	Weak transcription	Aorta	Aorta
25	chr9:71598800-71600200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr9:71598800-71600400	Enhancers	GM12878-XiMat	blood
27	chr9:71598800-71623200	Weak transcription	Pancreas	Pancrea
28	chr9:71598800-71644600	Weak transcription	Right Atrium	heart
29	chr9:71599000-71606000	Weak transcription	Rectal Mucosa Donor 31	rectum
30	chr9:71599000-71611000	Weak transcription	Primary hematopoietic stem cells	blood
31	chr9:71599000-71613000	Weak transcription	Left Ventricle	heart
32	chr9:71599400-71604200	Weak transcription	HepG2	liver
33	chr9:71599400-71605000	Weak transcription	Brain Germinal Matrix	brain
34	chr9:71599800-71600800	Strong transcription	Fetal Intestine Small	intestine
35	chr9:71600000-71612800	Weak transcription	K562	blood
36	chr9:71600200-71600600	Weak transcription	Fetal Heart	heart
37	chr9:71600200-71606000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr9:71600200-71606000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr9:71600200-71610000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
40	chr9:71600400-71600800	Strong transcription	Duodenum Mucosa	Duodenum
41	chr9:71600400-71600800	Genic enhancers	GM12878-XiMat	blood
42	chr9:71600600-71600800	Enhancers	Fetal Heart	heart
43	chr9:71600600-71601400	Strong transcription	Primary B cells from cord blood	blood
44	chr9:71600800-71601600	Enhancers	GM12878-XiMat	blood
45	chr9:71600800-71603400	Weak transcription	Fetal Intestine Small	intestine
46	chr9:71600800-71604800	Weak transcription	Fetal Heart	heart
47	chr9:71600800-71606000	Weak transcription	Duodenum Mucosa	Duodenum
48	chr9:71601000-71604200	Weak transcription	Fetal Intestine Large	intestine
49	chr9:71601200-71603800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr9:71601400-71605600	Weak transcription	Primary B cells from cord blood	blood

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