Variant report

Variant	nsv894664
Chromosome Location	chr9:140442503-140454791
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1203)
CpG islands
(count:613)
Chromatin interactive
region (count:48)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1203 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr9:140444794-140445032	K562	blood:	n/a	n/a
2	BACH1	chr9:140444871-140445043	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr9:140445891-140445908	K562	blood:	n/a	n/a
4	BACH1	chr9:140445812-140446093	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr9:140453668-140453847	GM12878	blood:	n/a	n/a
6	BCL3	chr9:140446495-140447277	A549	lung:	n/a	chr9:140446514-140446527
7	BCL3	chr9:140446470-140447336	A549	lung:	n/a	chr9:140446514-140446527
8	BCLAF1	chr9:140446664-140447061	GM12878	blood:	n/a	n/a
9	BHLHE40	chr9:140444689-140445061	HepG2	liver:	n/a	n/a
10	BHLHE40	chr9:140445842-140446042	GM12878	blood:	n/a	chr9:140445881-140445897
11	BHLHE40	chr9:140454110-140454295	K562	blood:	n/a	n/a
12	BHLHE40	chr9:140444730-140445039	GM12878	blood:	n/a	n/a
13	BHLHE40	chr9:140445821-140446098	K562	blood:	n/a	chr9:140445881-140445897
14	BHLHE40	chr9:140444679-140445082	K562	blood:	n/a	n/a
15	BHLHE40	chr9:140444731-140445029	A549	lung:	n/a	n/a
16	BHLHE40	chr9:140446341-140446464	K562	blood:	n/a	n/a
17	BRCA1	chr9:140445938-140446071	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr9:140449577-140449680	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr9:140444741-140444956	Hela-S3	cervix:	n/a	n/a
20	CBX3	chr9:140445754-140446101	K562	blood:	n/a	n/a
21	CBX3	chr9:140453597-140453983	K562	blood:	n/a	n/a
22	CBX3	chr9:140444784-140445046	K562	blood:	n/a	n/a
23	CBX3	chr9:140446570-140447020	K562	blood:	n/a	n/a
24	CCNT2	chr9:140444833-140444990	K562	blood:	n/a	n/a
25	CCNT2	chr9:140445684-140446909	K562	blood:	n/a	n/a
26	CEBPB	chr9:140442201-140442569	IMR90	lung:	n/a	chr9:140442378-140442389
27	CEBPB	chr9:140442209-140442570	HepG2	liver:	n/a	chr9:140442378-140442389
28	CEBPB	chr9:140442133-140442606	MCF-7	breast:	n/a	chr9:140442378-140442389
29	CEBPB	chr9:140446756-140446772	K562	blood:	n/a	n/a
30	CEBPB	chr9:140442208-140442554	K562	blood:	n/a	chr9:140442378-140442389
31	CEBPB	chr9:140445888-140445963	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr9:140442209-140442534	Hela-S3	cervix:	n/a	chr9:140442378-140442389
33	CEBPB	chr9:140442333-140442549	H1-hESC	embryonic stem cell:	n/a	chr9:140442378-140442389
34	CEBPB	chr9:140442227-140442551	A549	lung:	n/a	chr9:140442378-140442389
35	CEBPD	chr9:140446183-140446577	HepG2	liver:	n/a	n/a
36	CHD1	chr9:140446613-140446783	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD1	chr9:140446424-140446648	GM12878	blood:	n/a	n/a
38	CHD2	chr9:140446911-140446947	Hela-S3	cervix:	n/a	n/a
39	CHD2	chr9:140446311-140446853	HepG2	liver:	n/a	n/a
40	CHD2	chr9:140446217-140446497	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD2	chr9:140445897-140446058	HepG2	liver:	n/a	n/a
42	CHD2	chr9:140445738-140446999	GM12878	blood:	n/a	n/a
43	CHD2	chr9:140445726-140446611	Hela-S3	cervix:	n/a	n/a
44	CHD2	chr9:140445921-140447101	K562	blood:	n/a	n/a
45	CHD2	chr9:140444778-140445068	Hela-S3	cervix:	n/a	n/a
46	CREB1	chr9:140446174-140446540	H1-hESC	embryonic stem cell:	n/a	n/a
47	CREB1	chr9:140446187-140446937	A549	lung:	n/a	n/a
48	CREB1	chr9:140446182-140447240	HepG2	liver:	n/a	n/a
49	CREB1	chr9:140453699-140453836	A549	lung:	n/a	n/a
50	CREB1	chr9:140445710-140446093	A549	lung:	n/a	n/a

(count:613 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:140446993-140447043	HCPEpiC	choroid plexus:	n/a
2	chr9:140446823-140446873	U87	brain:	n/a
3	chr9:140446656-140446706	HL-60	blood:	n/a
4	chr9:140446993-140447043	HCPEpiC	choroid plexus:	n/a
5	chr9:140446823-140446873	U87	brain:	n/a
6	chr9:140446656-140446706	HL-60	blood:	n/a
7	chr9:140449460-140449510	AG10803	skin:	n/a
8	chr9:140444966-140445016	HEEpiC	esophagus:	n/a
9	chr9:140447608-140447658	IMR90	lung:	fetal
10	chr9:140449460-140449510	SK-N-SH_RA	brain:	n/a
11	chr9:140446993-140447043	A549	lung:	n/a
12	chr9:140449460-140449510	NHBE	bronchial:	n/a
13	chr9:140446656-140446706	HepG2	liver:	n/a
14	chr9:140444378-140444428	HRCEpiC	kidney:	n/a
15	chr9:140445760-140445810	Caco-2	colon:	n/a
16	chr9:140446240-140446290	ovcar-3	ovarian:	n/a
17	chr9:140446823-140446873	BJ	skin:	n/a
18	chr9:140446993-140447043	MCF-7	breast:	n/a
19	chr9:140446458-140446508	AG04449	skin:	fetal
20	chr9:140447608-140447658	AG04450	lung:	fetal
21	chr9:140445760-140445810	NB4	blood:	n/a
22	chr9:140447608-140447658	GM19239	blood:	n/a
23	chr9:140445760-140445810	GM12878	blood:	n/a
24	chr9:140444378-140444428	LNCaP	prostate:	n/a
25	chr9:140449460-140449510	SKMC	muscle:	n/a
26	chr9:140446656-140446706	Hepatocyte	liver:	n/a
27	chr9:140445760-140445810	NHBE	bronchial:	n/a
28	chr9:140446656-140446706	Hela-S3	cervix:	n/a
29	chr9:140446458-140446508	HEEpiC	esophagus:	n/a
30	chr9:140446993-140447043	GM19239	blood:	n/a
31	chr9:140446240-140446290	SK-N-SH_RA	brain:	n/a
32	chr9:140446458-140446508	U87	brain:	n/a
33	chr9:140446823-140446873	AG09309	skin:	n/a
34	chr9:140446823-140446873	H1-hESC	embryonic stem cell:	embryo
35	chr9:140446993-140447043	HMEC	breast:	n/a
36	chr9:140446656-140446706	PANC-1	pancreas:	n/a
37	chr9:140446458-140446508	SK-N-SH	brain:	n/a
38	chr9:140446240-140446290	H1-hESC	embryonic stem cell:	embryo
39	chr9:140447608-140447658	Jurkat	blood:	n/a
40	chr9:140444378-140444428	CMK	blood:	n/a
41	chr9:140445760-140445810	Hela-S3	cervix:	n/a
42	chr9:140446458-140446508	NT2-D1	testis:	n/a
43	chr9:140444966-140445016	NB4	blood:	n/a
44	chr9:140446656-140446706	PrEC	prostate:	n/a
45	chr9:140447608-140447658	SK-N-SH	brain:	n/a
46	chr9:140446458-140446508	GM19239	blood:	n/a
47	chr9:140445760-140445810	HCT-116	colon:	n/a
48	chr9:140446458-140446508	ProgFib	skin:	n/a
49	chr9:140447608-140447658	HRE	kidney:	n/a
50	chr9:140447608-140447658	BJ	skin:	n/a

(count:48 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:140444476..140446866-chr9:140469262..140473127,6	MCF-7	breast:
2	chr9:140130666..140131228-chr9:140445991..140446498,2	K562	blood:
3	chr9:140444055..140447780-chr9:140498087..140502451,7	MCF-7	breast:
4	chr14:81687170..81687965-chr9:140446133..140446842,2	Hela-S3	cervix:
5	chr9:140444557..140448587-chr9:140470804..140473699,6	MCF-7	breast:
6	chr9:140444420..140448721-chr9:140471876..140474832,3	K562	blood:
7	chr9:140444243..140447461-chr9:140473220..140477204,4	MCF-7	breast:
8	chr9:140447442..140450048-chr9:140483763..140485400,2	MCF-7	breast:
9	chr9:140445818..140448729-chr9:140451345..140453162,4	MCF-7	breast:
10	chr9:140443433..140448155-chr9:140497818..140502870,8	MCF-7	breast:
11	chr9:140170828..140173620-chr9:140446274..140448338,3	K562	blood:
12	chr9:140450468..140452580-chr9:140456810..140458829,2	MCF-7	breast:
13	chr9:140444986..140448753-chr9:140497892..140501428,4	K562	blood:
14	chr9:140443479..140444983-chr9:140499290..140501657,2	K562	blood:
15	chr9:140205840..140207870-chr9:140446473..140449405,2	MCF-7	breast:
16	chr9:140446189..140447738-chr9:140484697..140486582,2	K562	blood:
17	chr9:140448023..140449747-chr9:140465385..140467974,2	K562	blood:
18	chr9:140444995..140447677-chr9:140508337..140511208,2	MCF-7	breast:
19	chr9:140188507..140191128-chr9:140444764..140447765,3	MCF-7	breast:
20	chr9:140171323..140173620-chr9:140444809..140447880,3	K562	blood:
21	chr9:140395969..140398056-chr9:140445670..140447895,2	K562	blood:
22	chr9:140081713..140085345-chr9:140445556..140447863,3	MCF-7	breast:
23	chr9:140189775..140190406-chr9:140445582..140446845,3	K562	blood:
24	chr9:140446439..140449718-chr9:140469897..140473461,3	K562	blood:
25	chr9:140189588..140190355-chr9:140445590..140446295,2	MCF-7	breast:
26	chr9:140445810..140448101-chr9:140449501..140452314,4	K562	blood:
27	chr9:140443475..140446294-chr9:140484220..140486836,3	MCF-7	breast:
28	chr9:140444528..140447263-chr9:140504669..140508200,5	MCF-7	breast:
29	chr9:140448822..140451446-chr9:140457626..140459240,2	K562	blood:
30	chr9:140317304..140318861-chr9:140444413..140447408,2	K562	blood:
31	chr9:140355494..140357648-chr9:140446528..140449268,2	K562	blood:
32	chr9:140439935..140442817-chr9:140445009..140447280,2	MCF-7	breast:
33	chr9:140449572..140452200-chr9:140506963..140508845,2	MCF-7	breast:
34	chr19:48281795..48283367-chr9:140445657..140447919,2	MCF-7	breast:
35	chr9:140443477..140447796-chr9:140449022..140451330,7	MCF-7	breast:
36	chr9:140447049..140448753-chr9:140497892..140500070,2	K562	blood:
37	chr9:140443274..140446260-chr9:140471876..140474598,3	K562	blood:
38	chr9:140352080..140354787-chr9:140444624..140448715,3	MCF-7	breast:
39	chr9:140441799..140446269-chr9:140505086..140508400,5	MCF-7	breast:
40	chr8:135112230..135113008-chr9:140445827..140446528,2	MCF-7	breast:
41	chr9:140445818..140448729-chr9:140451345..140453162,4	MCF-7	breast:
42	chr9:140118466..140120300-chr9:140443395..140446342,2	MCF-7	breast:
43	chr9:140445810..140448101-chr9:140449501..140452314,4	K562	blood:
44	chr9:140439935..140442817-chr9:140445009..140447280,2	MCF-7	breast:
45	chr9:140445002..140446703-chr9:140512317..140515053,2	MCF-7	breast:
46	chr9:140193137..140197903-chr9:140443164..140449787,14	MCF-7	breast:
47	chr9:140188389..140190191-chr9:140444959..140446807,2	MCF-7	breast:
48	chr9:140447426..140450339-chr9:140645965..140648548,2	K562	blood:

No data

Variant related genes	Relation type
PNPLA7	TF binding region
MRPL41	TF binding region
PNPLA7	CpG island
MRPL41	CpG island
ENSG00000181090	chromatin interactions
ENSG00000198435	chromatin interactions
ENSG00000187609	chromatin interactions
ENSG00000260996	chromatin interactions
ENSG00000165724	chromatin interactions
ENSG00000165802	chromatin interactions
ENSG00000178980	chromatin interactions
ENSG00000198113	chromatin interactions
ENSG00000263933	chromatin interactions
ENSG00000165417	chromatin interactions
ENSG00000197070	chromatin interactions
ENSG00000188747	chromatin interactions
ENSG00000203993	chromatin interactions
ENSG00000176248	chromatin interactions
ENSG00000182154	chromatin interactions
ENSG00000130653	chromatin interactions
ENSG00000148399	chromatin interactions
ENSG00000176101	chromatin interactions
ENSG00000197191	chromatin interactions

Extended variants
information (count: 552 )
Associated
traits (count: 20 )

Variant overlapped rSNPs/rCNVs (count:552 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9410023	chr9:140442503-140442504	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs535762355	chr9:140442553-140442554	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs549226078	chr9:140442557-140442558	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs566267717	chr9:140442563-140442564	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs534954976	chr9:140442570-140442571	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs35361268	chr9:140442606-140442607	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs554307475	chr9:140442615-140442616	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs190868281	chr9:140442616-140442617	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs371010345	chr9:140442634-140442635	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs180921619	chr9:140442654-140442655	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs556210549	chr9:140442669-140442670	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs576064493	chr9:140442707-140442708	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs148472716	chr9:140442712-140442713	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs555744488	chr9:140442716-140442717	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs572293687	chr9:140442717-140442718	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs540905110	chr9:140442719-140442720	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs564287308	chr9:140442720-140442721	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs533290449	chr9:140442769-140442770	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs543479255	chr9:140442799-140442800	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs141778336	chr9:140442862-140442863	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs529203849	chr9:140442866-140442867	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs78641400	chr9:140442916-140442917	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs187259869	chr9:140442921-140442922	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs528760554	chr9:140442923-140442924	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs577119323	chr9:140442924-140442925	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs571778615	chr9:140442928-140442929	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs147205077	chr9:140442944-140442945	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs10867029	chr9:140442998-140442999	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs569761917	chr9:140443006-140443007	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs535482780	chr9:140443037-140443038	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs1776756	chr9:140443056-140443057	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs561850592	chr9:140443120-140443121	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs369592012	chr9:140443125-140443126	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs572281034	chr9:140443131-140443132	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs35323366	chr9:140443169-140443170	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs147785762	chr9:140443186-140443187	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs35745259	chr9:140443216-140443217	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs557686355	chr9:140443218-140443219	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs577378159	chr9:140443242-140443243	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs543513599	chr9:140443254-140443255	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs34029966	chr9:140443258-140443259	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs563488847	chr9:140443266-140443267	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs529339187	chr9:140443284-140443285	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs542639471	chr9:140443307-140443308	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs559669861	chr9:140443368-140443369	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs528796749	chr9:140443370-140443371	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs192054375	chr9:140443371-140443372	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs139052151	chr9:140443416-140443417	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs531174193	chr9:140443506-140443507	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs200725694	chr9:140443539-140443540	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:20)

Disease	PMID	Source
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Cardiac fibroma	18329553	CNVD
Lung cancer	19147751	CNVD
Cervical cancer	17311676	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Chordoma	18071362	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Sudden cardiac death	19188705	CNVD
Myoepithelioma	18604193	CNVD
Tuberous sclerosis	19566914	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Mantle cell lymphoma	19029149	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:1147 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:140376800-140444000	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr9:140408600-140444400	Weak transcription	Esophagus	oesophagus
3	chr9:140411200-140444200	Weak transcription	Right Atrium	heart
4	chr9:140429600-140443400	Weak transcription	Brain Germinal Matrix	brain
5	chr9:140429600-140444400	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr9:140429800-140443200	Weak transcription	Stomach Mucosa	stomach
7	chr9:140429800-140444200	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr9:140429800-140444200	Weak transcription	Colon Smooth Muscle	Colon
9	chr9:140429800-140444200	Weak transcription	Duodenum Smooth Muscle	Duodenum
10	chr9:140429800-140444200	Weak transcription	Fetal Lung	lung
11	chr9:140429800-140444200	Weak transcription	Rectal Smooth Muscle	rectum
12	chr9:140429800-140444600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr9:140429800-140444600	Weak transcription	NH-A	brain
14	chr9:140431600-140444200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
15	chr9:140431600-140444200	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr9:140431800-140443200	Weak transcription	Primary T helper cells fromperipheralblood	blood
17	chr9:140431800-140444200	Weak transcription	Primary T cells from cord blood	blood
18	chr9:140431800-140444800	Weak transcription	Dnd41	blood
19	chr9:140432200-140443400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
20	chr9:140433000-140443800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr9:140433000-140444200	Weak transcription	Brain Substantia Nigra	brain
22	chr9:140433200-140443400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
23	chr9:140435400-140444600	Weak transcription	Aorta	Aorta
24	chr9:140437400-140442600	Weak transcription	Rectal Mucosa Donor 29	rectum
25	chr9:140437400-140444600	Weak transcription	Fetal Kidney	kidney
26	chr9:140437800-140442600	Weak transcription	Lung	lung
27	chr9:140437800-140443400	Weak transcription	Rectal Mucosa Donor 31	rectum
28	chr9:140438000-140444200	Weak transcription	Fetal Brain Female	brain
29	chr9:140438400-140443400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr9:140438400-140443400	Weak transcription	Brain Angular Gyrus	brain
31	chr9:140438400-140444000	Weak transcription	Brain Cingulate Gyrus	brain
32	chr9:140438400-140444200	Weak transcription	Brain Hippocampus Middle	brain
33	chr9:140439000-140443200	Weak transcription	Colonic Mucosa	Colon
34	chr9:140439000-140444200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr9:140439000-140444200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr9:140439800-140444400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr9:140439800-140444400	Weak transcription	HSMM	muscle
38	chr9:140440000-140443400	Weak transcription	Fetal Muscle Trunk	muscle
39	chr9:140440000-140443400	Weak transcription	Fetal Muscle Leg	muscle
40	chr9:140440000-140444200	Weak transcription	HSMMtube	muscle
41	chr9:140440000-140444400	Weak transcription	Muscle Satellite Cultured Cells	--
42	chr9:140440400-140444400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr9:140441000-140442600	Enhancers	Breast Myoepithelial Primary Cells	Breast
44	chr9:140441200-140444200	Enhancers	Brain Inferior Temporal Lobe	brain
45	chr9:140441200-140444200	Weak transcription	Fetal Intestine Small	intestine
46	chr9:140441400-140444000	Enhancers	Primary B cells from peripheral blood	blood
47	chr9:140441400-140444400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr9:140441600-140443800	Weak transcription	Fetal Thymus	thymus
49	chr9:140441600-140444200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr9:140441600-140444200	Weak transcription	Fetal Stomach	stomach

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