Variant report

Variant	nsv540361
Chromosome Location	chr9:140376959-140415925
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:832)
CpG islands
(count:1345)
Chromatin interactive
region (count:116)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:832 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:140397266-140397473	K562	blood:	n/a	n/a
2	ARID3A	chr9:140388745-140388839	K562	blood:	n/a	n/a
3	ARID3A	chr9:140406300-140406534	K562	blood:	n/a	n/a
4	ATF1	chr9:140376674-140377053	K562	blood:	n/a	n/a
5	ATF1	chr9:140413661-140413862	K562	blood:	n/a	n/a
6	ATF1	chr9:140385237-140385607	K562	blood:	n/a	n/a
7	ATF1	chr9:140386077-140386838	K562	blood:	n/a	n/a
8	ATF1	chr9:140406110-140406643	K562	blood:	n/a	n/a
9	ATF3	chr9:140411303-140411539	K562	blood:	n/a	n/a
10	ATF3	chr9:140376711-140377025	K562	blood:	n/a	n/a
11	ATF3	chr9:140376631-140377006	K562	blood:	n/a	n/a
12	ATF3	chr9:140411269-140411670	K562	blood:	n/a	n/a
13	ATF3	chr9:140406167-140406614	K562	blood:	n/a	n/a
14	ATF3	chr9:140412120-140413744	K562	blood:	n/a	n/a
15	ATF3	chr9:140406275-140406755	K562	blood:	n/a	n/a
16	BACH1	chr9:140376512-140377007	K562	blood:	n/a	n/a
17	BACH1	chr9:140405284-140405477	K562	blood:	n/a	n/a
18	BATF	chr9:140406195-140406475	GM12878	blood:	n/a	n/a
19	BATF	chr9:140406312-140406518	GM12878	blood:	n/a	n/a
20	BCL3	chr9:140403490-140404024	GM12878	blood:	n/a	n/a
21	BCL3	chr9:140401077-140401330	GM12878	blood:	n/a	n/a
22	BHLHE40	chr9:140388628-140388967	K562	blood:	n/a	n/a
23	BHLHE40	chr9:140406121-140406881	K562	blood:	n/a	n/a
24	BHLHE40	chr9:140376779-140377018	A549	lung:	n/a	n/a
25	BHLHE40	chr9:140401074-140401443	HepG2	liver:	n/a	n/a
26	BHLHE40	chr9:140386093-140386833	K562	blood:	n/a	n/a
27	BHLHE40	chr9:140413599-140414372	K562	blood:	n/a	n/a
28	BHLHE40	chr9:140387537-140387771	K562	blood:	n/a	n/a
29	BHLHE40	chr9:140376543-140377273	K562	blood:	n/a	n/a
30	BHLHE40	chr9:140376682-140377094	HepG2	liver:	n/a	n/a
31	BRCA1	chr9:140396706-140397075	Hela-S3	cervix:	n/a	n/a
32	BRCA1	chr9:140405434-140405481	Hela-S3	cervix:	n/a	n/a
33	CBX3	chr9:140376496-140377104	K562	blood:	n/a	n/a
34	CBX3	chr9:140387464-140387854	K562	blood:	n/a	n/a
35	CBX3	chr9:140404370-140404806	K562	blood:	n/a	n/a
36	CBX3	chr9:140413277-140413859	K562	blood:	n/a	n/a
37	CBX3	chr9:140386246-140386901	K562	blood:	n/a	n/a
38	CBX3	chr9:140405335-140406878	K562	blood:	n/a	n/a
39	CBX3	chr9:140405383-140405862	K562	blood:	n/a	n/a
40	CBX3	chr9:140388325-140388963	K562	blood:	n/a	n/a
41	CBX3	chr9:140404369-140404739	K562	blood:	n/a	n/a
42	CBX3	chr9:140388579-140388820	K562	blood:	n/a	n/a
43	CCNT2	chr9:140386132-140386794	K562	blood:	n/a	chr9:140386518-140386538
44	CCNT2	chr9:140376819-140377100	K562	blood:	n/a	n/a
45	CCNT2	chr9:140388585-140388851	K562	blood:	n/a	n/a
46	CEBPB	chr9:140396538-140397084	Hela-S3	cervix:	n/a	chr9:140396806-140396818
47	CEBPB	chr9:140396723-140396820	K562	blood:	n/a	chr9:140396806-140396818
48	CEBPB	chr9:140413585-140413601	A549	lung:	n/a	n/a
49	CEBPB	chr9:140376625-140377105	K562	blood:	n/a	n/a
50	CEBPB	chr9:140376448-140377055	MCF-7	breast:	n/a	n/a

(count:1345 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:140399104-140399154	Hela-S3	cervix:	n/a
2	chr9:140380767-140380817	NB4	blood:	n/a
3	chr9:140392749-140392799	AG04449	skin:	fetal
4	chr9:140399104-140399154	Hela-S3	cervix:	n/a
5	chr9:140380767-140380817	NB4	blood:	n/a
6	chr9:140392749-140392799	AG04449	skin:	fetal
7	chr9:140406894-140406944	PANC-1	pancreas:	n/a
8	chr9:140401576-140401626	SK-N-SH	brain:	n/a
9	chr9:140408634-140408684	HEEpiC	esophagus:	n/a
10	chr9:140392749-140392799	HAEpiC	amniotic membrane:	n/a
11	chr9:140401576-140401626	MCF-7	breast:	n/a
12	chr9:140388523-140388573	AG09319	gingival:	n/a
13	chr9:140388604-140388654	HCF	heart:	n/a
14	chr9:140395754-140395804	HMEC	breast:	n/a
15	chr9:140401382-140401432	GM12891	blood:	n/a
16	chr9:140380767-140380817	AG09309	skin:	n/a
17	chr9:140400563-140400613	CMK	blood:	n/a
18	chr9:140400563-140400613	AoSMC	blood vessel:	n/a
19	chr9:140388604-140388654	NT2-D1	testis:	n/a
20	chr9:140408634-140408684	HNPCEpiC	eye:	n/a
21	chr9:140401382-140401432	HAEpiC	amniotic membrane:	n/a
22	chr9:140380767-140380817	AG04449	skin:	fetal
23	chr9:140406123-140406173	HRPEpiC	eye:	n/a
24	chr9:140401437-140401487	HUVEC	blood vessel:	n/a
25	chr9:140388523-140388573	NT2-D1	testis:	n/a
26	chr9:140400693-140400743	K562	blood:	n/a
27	chr9:140400693-140400743	HCPEpiC	choroid plexus:	n/a
28	chr9:140395219-140395269	HCPEpiC	choroid plexus:	n/a
29	chr9:140388523-140388573	NHDF-neo	bronchial:	n/a
30	chr9:140388604-140388654	HAEpiC	amniotic membrane:	n/a
31	chr9:140401437-140401487	SAEC	small airway:	n/a
32	chr9:140389750-140389800	IMR90	lung:	fetal
33	chr9:140401455-140401505	PFSK-1	brain:	n/a
34	chr9:140406123-140406173	HCM	heart:	n/a
35	chr9:140391480-140391530	AG09319	gingival:	n/a
36	chr9:140380767-140380817	NT2-D1	testis:	n/a
37	chr9:140408634-140408684	BJ	skin:	n/a
38	chr9:140409915-140409965	GM12891	blood:	n/a
39	chr9:140395219-140395269	Hepatocyte	liver:	n/a
40	chr9:140380767-140380817	NH-A	brain:	n/a
41	chr9:140406123-140406173	HCT-116	colon:	n/a
42	chr9:140395219-140395269	AG04449	skin:	fetal
43	chr9:140406123-140406173	RPTEC	kidney:	n/a
44	chr9:140388604-140388654	NB4	blood:	n/a
45	chr9:140400693-140400743	LNCaP	prostate:	n/a
46	chr9:140392749-140392799	AoSMC	blood vessel:	n/a
47	chr9:140401382-140401432	HL-60	blood:	n/a
48	chr9:140401437-140401487	Hepatocyte	liver:	n/a
49	chr9:140406645-140406695	Jurkat	blood:	n/a
50	chr9:140377789-140377839	HCM	heart:	n/a

(count:116 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr9:140347379..140350027-chr9:140394775..140397563,4	K562	blood:
2	chr9:140412465..140415104-chr9:140500104..140501750,2	MCF-7	breast:
3	chr9:140377265..140380212-chr9:140382477..140384358,2	MCF-7	breast:
4	chr9:140412905..140414820-chr9:140475554..140478292,2	K562	blood:
5	chr9:140348925..140356512-chr9:140392643..140399279,11	MCF-7	breast:
6	chr9:140358054..140360809-chr9:140375764..140378242,2	MCF-7	breast:
7	chr9:140192004..140196032-chr9:140413457..140417425,3	MCF-7	breast:
8	chr9:140386446..140388269-chr9:140413186..140415741,2	K562	blood:
9	chr9:140353655..140356104-chr9:140385846..140387400,2	MCF-7	breast:
10	chr9:140379847..140381560-chr9:140394727..140396348,2	MCF-7	breast:
11	chr9:140195239..140196828-chr9:140374464..140377100,2	MCF-7	breast:
12	chr9:140390425..140392825-chr9:140393171..140396140,3	MCF-7	breast:
13	chr17:41398685..41402669-chr9:140403955..140406978,23	K562	blood:
14	chr9:140332776..140334313-chr9:140412829..140415749,2	MCF-7	breast:
15	chr9:140386948..140388697-chr9:140392621..140394758,2	K562	blood:
16	chr9:140193294..140197517-chr9:140375531..140379734,5	K562	blood:
17	chr3:73158225..73159978-chr9:140403956..140405478,2	K562	blood:
18	chr9:140390425..140392825-chr9:140393171..140396140,3	MCF-7	breast:
19	chr9:140192575..140194190-chr9:140396987..140398919,2	MCF-7	breast:
20	chr17:41464359..41467817-chr9:140403952..140405475,5	MCF-7	breast:
21	chr9:140195173..140197851-chr9:140381665..140386088,4	MCF-7	breast:
22	chr9:140413558..140415139-chr9:140438109..140439773,2	MCF-7	breast:
23	chr9:140353512..140355543-chr9:140385777..140387498,2	MCF-7	breast:
24	chr9:140381904..140384229-chr9:140391274..140393120,2	MCF-7	breast:
25	chr9:140355725..140357240-chr9:140385390..140388277,2	K562	blood:
26	chr17:41464810..41468604-chr9:140403948..140406978,10	K562	blood:
27	chr9:140347395..140351065-chr9:140385610..140390076,3	K562	blood:
28	chr9:140406090..140408073-chr9:140408484..140412188,3	K562	blood:
29	chr9:140379847..140381560-chr9:140394727..140396348,2	MCF-7	breast:
30	chr11:62607627..62609127-chr9:140403971..140406953,2	K562	blood:
31	chr9:140189560..140193480-chr9:140384679..140388476,4	K562	blood:
32	chr9:140385373..140390339-chr9:140393084..140398390,8	MCF-7	breast:
33	chr9:140392839..140394933-chr9:140399102..140401511,2	K562	blood:
34	chr9:140189647..140191629-chr9:140408835..140411014,2	MCF-7	breast:
35	chr9:140392839..140394933-chr9:140399102..140401511,2	K562	blood:
36	chr9:140377045..140378867-chr9:140380603..140382500,2	K562	blood:
37	chr9:140402660..140405211-chr9:140405983..140408009,2	MCF-7	breast:
38	chr9:140320912..140322713-chr9:140405258..140407507,2	MCF-7	breast:
39	chr9:140390861..140392833-chr9:140394887..140396541,2	MCF-7	breast:
40	chr9:140396811..140398508-chr9:140398608..140401370,2	MCF-7	breast:
41	chr9:140353788..140359040-chr9:140385385..140389520,8	K562	blood:
42	chr9:140395969..140398056-chr9:140445670..140447895,2	K562	blood:
43	chr9:140374535..140376997-chr9:140379595..140382767,4	MCF-7	breast:
44	chr9:140385602..140387946-chr9:140412336..140414686,2	K562	blood:
45	chr9:140401353..140403296-chr9:140405117..140407444,2	K562	blood:
46	chr9:139681947..139682447-chr9:140405240..140405846,2	K562	blood:
47	chr9:140189399..140191424-chr9:140391666..140393367,2	K562	blood:
48	chr17:41398704..41402669-chr9:140403952..140406979,22	K562	blood:
49	chr9:140352371..140354173-chr9:140410410..140412850,2	MCF-7	breast:
50	chr9:140351004..140356661-chr9:140371273..140378307,10	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NOXA1-2	chr9:140383407-140384391	NONHSAT135733
2	lnc-NOXA1-2	chr9:140383003-140383341	NONHSAT135732
3	lnc-NELF-2	chr9:140382990-140383726	NONHSAT135731
4	lnc-NOXA1-2	chr9:140383224-140383341	NONHSAT135733
5	lnc-WDR85-1	chr9:140412889-140412899	NONHSAT135734
6	lnc-NELF-2	chr9:140385913-140386550	NONHSAT135731
7	lnc-WDR85-1	chr9:140411319-140412418	NONHSAT135734
8	lnc-NOXA1-2	chr9:140383507-140383567	NONHSAT135732

No data

Variant related genes	Relation type
PNPLA7	TF binding region
PNPLA7	CpG island
ENSG00000197070	chromatin interactions
ENSG00000149136	chromatin interactions
ENSG00000187609	chromatin interactions
ENSG00000130653	chromatin interactions
ENSG00000260996	chromatin interactions
ENSG00000236383	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000181090	chromatin interactions
ENSG00000198113	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000198435	chromatin interactions
ENSG00000203993	chromatin interactions
ENSG00000188833	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000263933	chromatin interactions
ENSG00000165802	chromatin interactions

Extended variants
information (count: 2028 )
Associated
traits (count: 20 )

Variant overlapped rSNPs/rCNVs (count:2028 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577447583	chr9:140376994-140376995	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs543887532	chr9:140376999-140377000	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs189637579	chr9:140377015-140377016	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs74709370	chr9:140377030-140377031	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs561117642	chr9:140377033-140377034	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs79666259	chr9:140377064-140377065	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs528775613	chr9:140377112-140377113	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs35998893	chr9:140377124-140377125	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs370979761	chr9:140377147-140377148	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs552139810	chr9:140377190-140377191	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs565470198	chr9:140377192-140377193	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs531059313	chr9:140377196-140377197	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs556556310	chr9:140377197-140377198	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs551158702	chr9:140377202-140377203	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs576376601	chr9:140377208-140377209	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs34127077	chr9:140377215-140377216	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs74566455	chr9:140377226-140377227	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs373919147	chr9:140377233-140377234	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs375400841	chr9:140377252-140377253	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs11137250	chr9:140377402-140377403	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs562167004	chr9:140377427-140377428	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs572563488	chr9:140377442-140377443	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs565364167	chr9:140377443-140377444	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs377628096	chr9:140377448-140377449	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs534587796	chr9:140377474-140377475	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs11998929	chr9:140377512-140377513	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs143409795	chr9:140377513-140377514	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs11137252	chr9:140377542-140377543	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs536796409	chr9:140377554-140377555	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs557125524	chr9:140377603-140377604	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs574025262	chr9:140377660-140377661	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs541274055	chr9:140377676-140377677	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs17065427	chr9:140377720-140377721	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs371031787	chr9:140377726-140377727	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs530023033	chr9:140377745-140377746	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs545713913	chr9:140377789-140377790	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs565532074	chr9:140377839-140377840	Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs564104004	chr9:140377885-140377886	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs531246177	chr9:140377897-140377898	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs180759809	chr9:140377938-140377939	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs561553120	chr9:140377951-140377952	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs533289954	chr9:140377952-140377953	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs528959421	chr9:140377970-140377971	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs12345175	chr9:140378098-140378099	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs112319577	chr9:140378111-140378112	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs543789264	chr9:140378155-140378156	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs375000589	chr9:140378156-140378157	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs368203729	chr9:140378170-140378171	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs543366138	chr9:140378226-140378227	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs144767983	chr9:140378260-140378261	Weak transcription	Chromatin interactive region	2 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:642 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:140356600-140377000	Weak transcription	Rectal Smooth Muscle	rectum
2	chr9:140370800-140383400	Weak transcription	Duodenum Smooth Muscle	Duodenum
3	chr9:140371000-140385800	Weak transcription	Primary B cells from peripheral blood	blood
4	chr9:140371200-140382200	Weak transcription	Brain Anterior Caudate	brain
5	chr9:140371200-140383200	Weak transcription	Primary B cells from cord blood	blood
6	chr9:140371800-140382000	Weak transcription	Fetal Intestine Small	intestine
7	chr9:140373000-140377600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr9:140373200-140377400	Bivalent Enhancer	Placenta	Placenta
9	chr9:140373800-140377000	Weak transcription	Colonic Mucosa	Colon
10	chr9:140373800-140377600	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr9:140373800-140396000	Weak transcription	Esophagus	oesophagus
12	chr9:140374000-140377200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr9:140374000-140386200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr9:140374600-140385800	Weak transcription	Brain Hippocampus Middle	brain
15	chr9:140374800-140377000	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr9:140375000-140392200	Weak transcription	Brain Angular Gyrus	brain
17	chr9:140375400-140382200	Weak transcription	Lung	lung
18	chr9:140375400-140386000	Weak transcription	Aorta	Aorta
19	chr9:140375400-140387600	Weak transcription	Sigmoid Colon	Sigmoid Colon
20	chr9:140375600-140377200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr9:140375600-140379000	Weak transcription	Pancreas	Pancrea
22	chr9:140375800-140377200	Enhancers	Fetal Muscle Trunk	muscle
23	chr9:140375800-140377400	Enhancers	HMEC	breast
24	chr9:140375800-140377600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr9:140376000-140379000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr9:140376400-140377000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr9:140376400-140377000	Enhancers	Brain Substantia Nigra	brain
28	chr9:140376400-140377000	Enhancers	Rectal Mucosa Donor 29	rectum
29	chr9:140376400-140377000	Enhancers	Stomach Mucosa	stomach
30	chr9:140376400-140377200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr9:140376400-140377200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr9:140376400-140377200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr9:140376400-140377200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr9:140376400-140377200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr9:140376400-140377200	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr9:140376400-140377200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr9:140376400-140377200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr9:140376400-140377200	Enhancers	Muscle Satellite Cultured Cells	--
39	chr9:140376400-140377200	Enhancers	Adipose Nuclei	Adipose
40	chr9:140376400-140377200	Enhancers	Liver	Liver
41	chr9:140376400-140377200	Enhancers	Fetal Muscle Leg	muscle
42	chr9:140376400-140377200	Enhancers	Ovary	ovary
43	chr9:140376400-140377200	Enhancers	Skeletal Muscle Male	skeletal muscle
44	chr9:140376400-140377200	Flanking Active TSS	Hela-S3	cervix
45	chr9:140376400-140377200	Enhancers	HSMMtube	muscle
46	chr9:140376400-140377200	Flanking Active TSS	K562	blood
47	chr9:140376400-140377400	Enhancers	Primary monocytes fromperipheralblood	blood
48	chr9:140376400-140377400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr9:140376400-140377800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr9:140376400-140377800	Enhancers	HepG2	liver

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