Variant report

Variant	nsv893745
Chromosome Location	chr9:115955271-116005783
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:901)
CpG islands
(count:305)
Chromatin interactive
region (count:70)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:901 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:115990291-115990958	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:115993968-115994315	K562	blood:	n/a	n/a
3	ARID3A	chr9:115984342-115985124	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:115983506-115983747	K562	blood:	n/a	n/a
5	ARID3A	chr9:115983338-115984123	HepG2	liver:	n/a	n/a
6	ATF1	chr9:115990413-115990708	K562	blood:	n/a	n/a
7	ATF1	chr9:115983423-115983901	K562	blood:	n/a	n/a
8	ATF2	chr9:115983017-115983980	H1-hESC	embryonic stem cell:	n/a	chr9:115983730-115983741
9	ATF2	chr9:115983304-115984037	GM12878	blood:	n/a	chr9:115983730-115983741
10	ATF2	chr9:115981259-115982696	GM12878	blood:	n/a	n/a
11	ATF2	chr9:115981374-115982764	GM12878	blood:	n/a	n/a
12	ATF2	chr9:115983357-115983928	GM12878	blood:	n/a	chr9:115983730-115983741
13	ATF2	chr9:115983337-115983806	H1-hESC	embryonic stem cell:	n/a	chr9:115983730-115983741
14	ATF3	chr9:115983301-115983851	H1-hESC	embryonic stem cell:	n/a	chr9:115983729-115983740 chr9:115983731-115983739 chr9:115983729-115983742 chr9:115983730-115983741 chr9:115983731-115983742 chr9:115983729-115983742 chr9:115983732-115983739
15	ATF3	chr9:115983220-115983829	HepG2	liver:	n/a	chr9:115983729-115983740 chr9:115983731-115983739 chr9:115983729-115983742 chr9:115983730-115983741 chr9:115983731-115983742 chr9:115983729-115983742 chr9:115983732-115983739
16	ATF3	chr9:115983213-115983792	GM12878	blood:	n/a	chr9:115983729-115983740 chr9:115983731-115983739 chr9:115983729-115983742 chr9:115983730-115983741 chr9:115983731-115983742 chr9:115983729-115983742 chr9:115983732-115983739
17	ATF3	chr9:115983440-115983712	GM12878	blood:	n/a	n/a
18	ATF3	chr9:115983170-115983797	K562	blood:	n/a	chr9:115983729-115983740 chr9:115983731-115983739 chr9:115983729-115983742 chr9:115983730-115983741 chr9:115983731-115983742 chr9:115983729-115983742 chr9:115983732-115983739
19	ATF3	chr9:115983440-115983907	K562	blood:	n/a	chr9:115983729-115983740 chr9:115983731-115983739 chr9:115983729-115983742 chr9:115983730-115983741 chr9:115983731-115983742 chr9:115983729-115983742 chr9:115983732-115983739
20	ATF3	chr9:115984765-115985094	K562	blood:	n/a	n/a
21	ATF3	chr9:115983419-115983792	H1-hESC	embryonic stem cell:	n/a	chr9:115983729-115983740 chr9:115983731-115983739 chr9:115983729-115983742 chr9:115983730-115983741 chr9:115983731-115983742 chr9:115983729-115983742 chr9:115983732-115983739
22	ATF3	chr9:115983233-115983781	HepG2	liver:	n/a	chr9:115983729-115983740 chr9:115983731-115983739 chr9:115983729-115983742 chr9:115983730-115983741 chr9:115983731-115983742 chr9:115983729-115983742 chr9:115983732-115983739
23	BACH1	chr9:115977469-115977786	K562	blood:	n/a	n/a
24	BACH1	chr9:115982879-115982887	K562	blood:	n/a	n/a
25	BACH1	chr9:115984091-115984099	K562	blood:	n/a	n/a
26	BACH1	chr9:115977514-115977791	H1-hESC	embryonic stem cell:	n/a	n/a
27	BATF	chr9:115981439-115981805	GM12878	blood:	n/a	chr9:115981724-115981732
28	BATF	chr9:115981447-115981779	GM12878	blood:	n/a	chr9:115981724-115981732
29	BATF	chr9:115982119-115982632	GM12878	blood:	n/a	n/a
30	BATF	chr9:115982206-115982623	GM12878	blood:	n/a	n/a
31	BCL11A	chr9:115981417-115981873	GM12878	blood:	n/a	chr9:115981634-115981643
32	BCL11A	chr9:115982153-115982635	GM12878	blood:	n/a	n/a
33	BCLAF1	chr9:115983290-115983801	GM12878	blood:	n/a	chr9:115983759-115983768 chr9:115983750-115983763 chr9:115983606-115983615
34	BCLAF1	chr9:115981212-115982657	GM12878	blood:	n/a	chr9:115981634-115981643
35	BCLAF1	chr9:115981455-115982653	GM12878	blood:	n/a	chr9:115981634-115981643
36	BHLHE40	chr9:115982855-115984189	K562	blood:	n/a	chr9:115984103-115984119
37	BHLHE40	chr9:115983525-115983870	A549	lung:	n/a	n/a
38	BHLHE40	chr9:115984504-115984694	K562	blood:	n/a	n/a
39	BHLHE40	chr9:115990316-115990750	HepG2	liver:	n/a	n/a
40	BHLHE40	chr9:115990322-115990675	K562	blood:	n/a	n/a
41	BHLHE40	chr9:115995278-115995394	GM12878	blood:	n/a	n/a
42	BHLHE40	chr9:115983468-115983999	HepG2	liver:	n/a	n/a
43	BHLHE40	chr9:115982127-115984239	GM12878	blood:	n/a	chr9:115984103-115984119
44	BHLHE40	chr9:115981434-115981876	GM12878	blood:	n/a	n/a
45	BRCA1	chr9:115983208-115984068	Hela-S3	cervix:	n/a	n/a
46	BRCA1	chr9:115983384-115983407	HepG2	liver:	n/a	n/a
47	BRCA1	chr9:115983701-115984066	HepG2	liver:	n/a	n/a
48	BRCA1	chr9:115984414-115984624	Hela-S3	cervix:	n/a	n/a
49	BRCA1	chr9:115983809-115983814	H1-hESC	embryonic stem cell:	n/a	n/a
50	CBX3	chr9:115983381-115984015	K562	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:115984268-115984318	BJ	skin:	n/a
2	chr9:115983049-115983099	T-47D	breast:	n/a
3	chr9:115983636-115983686	ovcar-3	ovarian:	n/a
4	chr9:115983049-115983099	SAEC	small airway:	n/a
5	chr9:115984268-115984318	GM06990	blood:	n/a
6	chr9:115984268-115984318	GM12878	blood:	n/a
7	chr9:115983049-115983099	AG10803	skin:	n/a
8	chr9:115987035-115987085	ovcar-3	ovarian:	n/a
9	chr9:115983636-115983686	HCT-116	colon:	n/a
10	chr9:115984268-115984318	Hepatocyte	liver:	n/a
11	chr9:115983636-115983686	HNPCEpiC	eye:	n/a
12	chr9:115983049-115983099	HRPEpiC	eye:	n/a
13	chr9:115983984-115984034	HL-60	blood:	n/a
14	chr9:115983049-115983099	PFSK-1	brain:	n/a
15	chr9:115983984-115984034	HEK293	kidney:	embryo
16	chr9:115983636-115983686	H1-hESC	embryonic stem cell:	embryo
17	chr9:115987035-115987085	PrEC	prostate:	n/a
18	chr9:115983049-115983099	HIPEpiC	eye:	n/a
19	chr9:115983984-115984034	LNCaP	prostate:	n/a
20	chr9:115984268-115984318	SK-N-SH_RA	brain:	n/a
21	chr9:115983636-115983686	RPTEC	kidney:	n/a
22	chr9:115987035-115987085	AG10803	skin:	n/a
23	chr9:115983049-115983099	SK-N-SH_RA	brain:	n/a
24	chr9:115983049-115983099	SK-N-SH	brain:	n/a
25	chr9:115983984-115984034	NHDF-neo	bronchial:	n/a
26	chr9:115983636-115983686	HRCEpiC	kidney:	n/a
27	chr9:115983049-115983099	NT2-D1	testis:	n/a
28	chr9:115983984-115984034	CMK	blood:	n/a
29	chr9:115984268-115984318	Jurkat	blood:	n/a
30	chr9:115983049-115983099	HEEpiC	esophagus:	n/a
31	chr9:115983636-115983686	AG09309	skin:	n/a
32	chr9:115987035-115987085	Jurkat	blood:	n/a
33	chr9:115984268-115984318	GM19239	blood:	n/a
34	chr9:115983984-115984034	SK-N-MC	brain:	n/a
35	chr9:115983049-115983099	HUVEC	blood vessel:	n/a
36	chr9:115983636-115983686	CMK	blood:	n/a
37	chr9:115983049-115983099	GM19239	blood:	n/a
38	chr9:115983636-115983686	PrEC	prostate:	n/a
39	chr9:115983636-115983686	T-47D	breast:	n/a
40	chr9:115984268-115984318	A549	lung:	n/a
41	chr9:115983636-115983686	AG04449	skin:	fetal
42	chr9:115987035-115987085	MCF-7	breast:	n/a
43	chr9:115984268-115984318	HCT-116	colon:	n/a
44	chr9:115983636-115983686	Jurkat	blood:	n/a
45	chr9:115983984-115984034	T-47D	breast:	n/a
46	chr9:115987035-115987085	H1-hESC	embryonic stem cell:	embryo
47	chr9:115984268-115984318	HRPEpiC	eye:	n/a
48	chr9:115987035-115987085	IMR90	lung:	fetal
49	chr9:115983049-115983099	HCT-116	colon:	n/a
50	chr9:115983636-115983686	HRPEpiC	eye:	n/a

(count:70 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr9:115990891..115993253-chr9:115993931..115999009,4	K562	blood:
2	chr9:115982005..115986983-chr9:116035777..116039702,5	K562	blood:
3	chr9:115951377..115953931-chr9:115974239..115975925,2	MCF-7	breast:
4	chr9:115974346..115976683-chr9:115980205..115982463,2	MCF-7	breast:
5	chr9:115983607..115986374-chr9:116170251..116172763,3	MCF-7	breast:
6	chr9:115953587..115956055-chr9:116171770..116173281,2	MCF-7	breast:
7	chr9:115990891..115993253-chr9:115993931..115999009,4	K562	blood:
8	chr9:115981728..115986983-chr9:116035777..116040437,9	K562	blood:
9	chr9:115988910..115990516-chr9:115992954..115994537,2	MCF-7	breast:
10	chr9:115961079..115963509-chr9:115965175..115968224,3	MCF-7	breast:
11	chr9:115995531..115997450-chr9:115998162..116001080,2	MCF-7	breast:
12	chr9:115968725..115971196-chr9:115981878..115984279,2	MCF-7	breast:
13	chr9:115961079..115963509-chr9:115965175..115968224,3	MCF-7	breast:
14	chr9:115979271..115982033-chr9:115982056..115983606,2	MCF-7	breast:
15	chr9:115983488..115985496-chr9:116035418..116038927,3	MCF-7	breast:
16	chr9:115963672..115965977-chr9:115972388..115974143,2	MCF-7	breast:
17	chr9:115955703..115958661-chr9:115961003..115965387,3	MCF-7	breast:
18	chr9:115959480..115961457-chr9:115966488..115968182,2	K562	blood:
19	chr9:115996965..115999527-chr9:116002148..116004164,2	K562	blood:
20	chr9:115982263..115984734-chr9:116036359..116038354,4	MCF-7	breast:
21	chr9:115967370..115970332-chr9:115970623..115973932,3	K562	blood:
22	chr9:115938881..115940407-chr9:115956072..115958715,2	MCF-7	breast:
23	chr9:115995531..115997450-chr9:115998162..116001080,2	MCF-7	breast:
24	chr9:115988089..115990143-chr9:115997118..115999123,2	MCF-7	breast:
25	chr9:115986078..115988319-chr9:115992917..115996032,3	MCF-7	breast:
26	chr9:115980759..115986590-chr9:115988652..115992433,8	K562	blood:
27	chr9:115976079..115978566-chr9:116036874..116039120,2	MCF-7	breast:
28	chr9:115979802..115981343-chr9:115983049..115985677,2	K562	blood:
29	chr9:116003514..116005216-chr9:116035646..116037704,2	MCF-7	breast:
30	chr9:115978706..115980364-chr9:115981064..115982891,2	K562	blood:
31	chr9:116001272..116004183-chr9:116010675..116013051,2	MCF-7	breast:
32	chr9:115956014..115959253-chr9:115961029..115963531,3	K562	blood:
33	chr9:115965291..115966796-chr9:115969248..115971645,2	K562	blood:
34	chr9:115993143..115995233-chr9:116002735..116005457,2	K562	blood:
35	chr9:115980360..115986264-chr9:116170629..116175189,6	K562	blood:
36	chr9:115978706..115980364-chr9:115981064..115982891,2	K562	blood:
37	chr9:115988089..115990143-chr9:115997118..115999123,2	MCF-7	breast:
38	chr9:115981852..115985156-chr9:116171660..116173942,3	MCF-7	breast:
39	chr9:115975066..115976588-chr9:115978815..115981431,2	MCF-7	breast:
40	chr9:115995999..115998465-chr9:116001136..116003648,2	K562	blood:
41	chr9:115983573..115985886-chr9:115986006..115988568,3	MCF-7	breast:
42	chr9:115981081..115983502-chr9:115983537..115987172,3	MCF-7	breast:
43	chr9:115991545..115993932-chr9:115995693..115997298,2	K562	blood:
44	chr9:115996965..115999527-chr9:116002148..116004164,2	K562	blood:
45	chr9:115988910..115990516-chr9:115992954..115994537,2	MCF-7	breast:
46	chr9:115952251..115954367-chr9:115960312..115963132,2	K562	blood:
47	chr9:115983851..115985489-chr9:115994207..115996988,2	MCF-7	breast:
48	chr12:53894115..53894858-chr9:115983781..115984688,2	Hela-S3	cervix:
49	chr9:115974346..115976683-chr9:115980205..115982463,2	MCF-7	breast:
50	chr9:115985715..115987380-chr9:116017322..116019580,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC31A1-1	chr9:115989558-115989940	NONHSAT134329
2	lnc-SLC31A1-1	chr9:115983808-115983958	NONHSAT134328
3	lnc-CDC26-2	chr9:115969492-115969576	NONHSAT134327
4	lnc-CDC26-2	chr9:115968291-115968858	NONHSAT134327
5	lnc-SLC31A1-1	chr9:115983867-115983958	NONHSAT134329

No data

Variant related genes	Relation type
FKBP15	TF binding region
SLC31A1	TF binding region
FKBP15	CpG island
SLC31A1	CpG island
ENSG00000167797	chromatin interactions
ENSG00000148229	chromatin interactions
ENSG00000176386	chromatin interactions
ENSG00000157653	chromatin interactions
ENSG00000119321	chromatin interactions
ENSG00000139546	chromatin interactions
ENSG00000136875	chromatin interactions
ENSG00000270175	chromatin interactions
ENSG00000136868	chromatin interactions

Extended variants
information (count: 1860 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:1860 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16926630	chr9:115955271-115955272	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs535302928	chr9:115955295-115955296	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs140756036	chr9:115955325-115955326	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs571579626	chr9:115955376-115955377	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs372810564	chr9:115955423-115955424	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs537449245	chr9:115955426-115955427	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs183052990	chr9:115955473-115955474	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs557214584	chr9:115955514-115955515	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs16926672	chr9:115955526-115955527	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs541625444	chr9:115955542-115955543	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs12346816	chr9:115955553-115955554	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs369010985	chr9:115955592-115955593	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs112281734	chr9:115955619-115955620	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs571896357	chr9:115955643-115955644	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs373345393	chr9:115955665-115955666	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs564404194	chr9:115955667-115955668	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs532831834	chr9:115955687-115955688	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs543365812	chr9:115955712-115955713	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs374848316	chr9:115955713-115955714	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs114395642	chr9:115955752-115955753	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs371216171	chr9:115955768-115955769	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs375529706	chr9:115955816-115955817	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs80167025	chr9:115955841-115955842	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs373279246	chr9:115955900-115955901	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs549615084	chr9:115955922-115955923	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs150457255	chr9:115955926-115955927	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs576024596	chr9:115955935-115955936	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs145319808	chr9:115955975-115955976	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs116192048	chr9:115955986-115955987	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs571898911	chr9:115955989-115955990	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs537058275	chr9:115956006-115956007	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs557274474	chr9:115956046-115956047	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs187747581	chr9:115956049-115956050	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs536309987	chr9:115956106-115956107	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs191355475	chr9:115956130-115956131	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs183718797	chr9:115956178-115956179	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs187696649	chr9:115956188-115956189	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs372413987	chr9:115956247-115956248	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs114976009	chr9:115956249-115956250	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs577822419	chr9:115956266-115956267	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs377326305	chr9:115956280-115956281	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs201737331	chr9:115956282-115956283	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs556332439	chr9:115956291-115956292	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs574831502	chr9:115956320-115956321	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs373790840	chr9:115956399-115956400	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs62636616	chr9:115956400-115956401	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs114054992	chr9:115956406-115956407	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs374760090	chr9:115956409-115956410	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs149222255	chr9:115956435-115956436	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs528719122	chr9:115956496-115956497	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Oral squamous cell carcinoma	17134496	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
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
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
small cell lung cancer	20016488	CNVD
Cardiac fibroma	18329553	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Lung cancer	19147751	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16272173	CNVD
Bladder cancer	21909424	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1824 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:115920000-115970200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr9:115920000-115973400	Strong transcription	Rectal Mucosa Donor 29	rectum
3	chr9:115920200-115956600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr9:115920400-115973400	Strong transcription	Primary T helper cells fromperipheralblood	blood
5	chr9:115920800-115966400	Strong transcription	Dnd41	blood
6	chr9:115920800-115975000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr9:115922800-115956400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
8	chr9:115923000-115956200	Strong transcription	Primary T helper cells PMA-I stimulated	--
9	chr9:115923400-115976400	Strong transcription	Primary T cells fromperipheralblood	blood
10	chr9:115924000-115965800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr9:115924200-115969600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr9:115926000-115956200	Strong transcription	HUES64 Cell Line	embryonic stem cell
13	chr9:115927600-115973400	Strong transcription	Skeletal Muscle Female	skeletal muscle
14	chr9:115936800-115982400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr9:115941200-115968600	Strong transcription	Primary B cells from peripheral blood	blood
16	chr9:115941200-115969200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr9:115942000-115956400	Strong transcription	Rectal Mucosa Donor 31	rectum
18	chr9:115942400-115956000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
19	chr9:115943200-115956800	Strong transcription	Duodenum Mucosa	Duodenum
20	chr9:115945400-115977200	Weak transcription	Stomach Mucosa	stomach
21	chr9:115945600-115982800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr9:115946000-115963600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
23	chr9:115947800-115956600	Strong transcription	Brain Angular Gyrus	brain
24	chr9:115949800-115961800	Weak transcription	Small Intestine	intestine
25	chr9:115950400-115972800	Weak transcription	Right Ventricle	heart
26	chr9:115950600-115959400	Weak transcription	Placenta Amnion	Placenta Amnion
27	chr9:115950600-115968600	Weak transcription	Fetal Heart	heart
28	chr9:115950600-115982400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr9:115950800-115955600	Weak transcription	Brain Inferior Temporal Lobe	brain
30	chr9:115950800-115956000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr9:115950800-115956400	Weak transcription	Pancreatic Islets	Pancreatic Islet
32	chr9:115950800-115961800	Weak transcription	H1 Cell Line	embryonic stem cell
33	chr9:115950800-115963400	Weak transcription	H9 Cell Line	embryonic stem cell
34	chr9:115950800-115963600	Weak transcription	Spleen	Spleen
35	chr9:115950800-115982800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr9:115951000-115955400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
37	chr9:115951000-115955600	Weak transcription	Esophagus	oesophagus
38	chr9:115951000-115956000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr9:115951000-115957600	Weak transcription	NHLF	lung
40	chr9:115951000-115959000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr9:115951000-115959200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr9:115951000-115972200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr9:115951000-115972200	Weak transcription	Gastric	stomach
44	chr9:115951000-115972200	Weak transcription	Pancreas	Pancrea
45	chr9:115951000-115974000	Strong transcription	Placenta	Placenta
46	chr9:115951000-115982800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
47	chr9:115951200-115955600	Strong transcription	Primary hematopoietic stem cells	blood
48	chr9:115951200-115959000	Weak transcription	Fetal Kidney	kidney
49	chr9:115951200-115959200	Weak transcription	Colonic Mucosa	Colon
50	chr9:115951200-115964800	Weak transcription	Fetal Brain Male	brain

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