Variant report

Variant	nsv1002970
Chromosome Location	chr3:47120592-47170607
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:47145094-47145536	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:47159207-47159826	K562	blood:	n/a	n/a
3	ARID3A	chr3:47143694-47144068	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:47142903-47143265	HepG2	liver:	n/a	n/a
5	ATF1	chr3:47159343-47159662	K562	blood:	n/a	n/a
6	BACH1	chr3:47161895-47162469	K562	blood:	n/a	n/a
7	BACH1	chr3:47163355-47163527	K562	blood:	n/a	n/a
8	BATF	chr3:47124036-47124433	GM12878	blood:	n/a	n/a
9	BATF	chr3:47124091-47124363	GM12878	blood:	n/a	n/a
10	BATF	chr3:47142908-47143130	GM12878	blood:	n/a	n/a
11	BCL11A	chr3:47155147-47155456	GM12878	blood:	n/a	chr3:47155335-47155344
12	CBX3	chr3:47160847-47161398	K562	blood:	n/a	n/a
13	CBX3	chr3:47160907-47161254	K562	blood:	n/a	n/a
14	CCNT2	chr3:47159323-47159735	K562	blood:	n/a	n/a
15	CEBPB	chr3:47163300-47163642	K562	blood:	n/a	chr3:47163481-47163492
16	CEBPB	chr3:47163393-47163598	HepG2	liver:	n/a	chr3:47163481-47163492
17	CEBPB	chr3:47133607-47133967	IMR90	lung:	n/a	chr3:47133782-47133791 chr3:47133780-47133793 chr3:47133782-47133791 chr3:47133782-47133791 chr3:47133639-47133650 chr3:47133780-47133793 chr3:47133781-47133792 chr3:47133782-47133791 chr3:47133780-47133791
18	CEBPB	chr3:47133659-47133865	H1-hESC	embryonic stem cell:	n/a	chr3:47133782-47133791 chr3:47133780-47133793 chr3:47133782-47133791 chr3:47133782-47133791 chr3:47133780-47133793 chr3:47133781-47133792 chr3:47133782-47133791 chr3:47133780-47133791
19	CEBPB	chr3:47163327-47163575	A549	lung:	n/a	chr3:47163481-47163492
20	CEBPB	chr3:47128361-47128554	H1-hESC	embryonic stem cell:	n/a	chr3:47128481-47128492
21	CEBPB	chr3:47133624-47133914	Hela-S3	cervix:	n/a	chr3:47133782-47133791 chr3:47133780-47133793 chr3:47133782-47133791 chr3:47133782-47133791 chr3:47133639-47133650 chr3:47133780-47133793 chr3:47133781-47133792 chr3:47133782-47133791 chr3:47133780-47133791
22	CEBPB	chr3:47128364-47128687	ECC-1	luminal epithelium:	n/a	chr3:47128481-47128492
23	CEBPB	chr3:47125489-47125579	HepG2	liver:	n/a	n/a
24	CEBPB	chr3:47152896-47153038	K562	blood:	n/a	n/a
25	CEBPB	chr3:47133604-47133938	K562	blood:	n/a	chr3:47133782-47133791 chr3:47133780-47133793 chr3:47133782-47133791 chr3:47133782-47133791 chr3:47133639-47133650 chr3:47133780-47133793 chr3:47133781-47133792 chr3:47133782-47133791 chr3:47133780-47133791
26	CEBPB	chr3:47128359-47128629	K562	blood:	n/a	chr3:47128481-47128492
27	CEBPB	chr3:47128336-47128584	HepG2	liver:	n/a	chr3:47128481-47128492
28	CEBPB	chr3:47128322-47128640	IMR90	lung:	n/a	chr3:47128481-47128492
29	CEBPB	chr3:47123964-47124541	IMR90	lung:	n/a	n/a
30	CEBPB	chr3:47133607-47133954	HepG2	liver:	n/a	chr3:47133782-47133791 chr3:47133780-47133793 chr3:47133782-47133791 chr3:47133782-47133791 chr3:47133639-47133650 chr3:47133780-47133793 chr3:47133781-47133792 chr3:47133782-47133791 chr3:47133780-47133791
31	CEBPB	chr3:47145139-47145629	HepG2	liver:	n/a	n/a
32	CEBPB	chr3:47133624-47133897	A549	lung:	n/a	chr3:47133782-47133791 chr3:47133780-47133793 chr3:47133782-47133791 chr3:47133782-47133791 chr3:47133639-47133650 chr3:47133780-47133793 chr3:47133781-47133792 chr3:47133782-47133791 chr3:47133780-47133791
33	CEBPB	chr3:47143820-47144046	HepG2	liver:	n/a	chr3:47143919-47143930
34	CEBPD	chr3:47159210-47159784	K562	blood:	n/a	n/a
35	CEBPD	chr3:47159159-47159792	K562	blood:	n/a	n/a
36	CHD1	chr3:47124482-47124500	GM12878	blood:	n/a	n/a
37	CHD1	chr3:47142714-47142740	GM12878	blood:	n/a	n/a
38	CHD2	chr3:47142952-47143206	GM12878	blood:	n/a	n/a
39	CHD2	chr3:47162172-47162353	K562	blood:	n/a	n/a
40	CTCF	chr3:47125360-47125510	GM12872	blood:	n/a	n/a
41	CTCF	chr3:47128926-47129054	MCF-7	breast:	n/a	n/a
42	CTCF	chr3:47123820-47123970	GM12875	blood:	n/a	n/a
43	CTCF	chr3:47123800-47123950	AG10803	skin:	n/a	n/a
44	CTCF	chr3:47123880-47124030	AG04450	lung:	n/a	n/a
45	CTCF	chr3:47123800-47123950	AG09319	gingival:	n/a	n/a
46	CTCF	chr3:47128940-47129090	A549	lung:	n/a	n/a
47	CTCF	chr3:47123780-47123930	HPF	lung:	n/a	n/a
48	CTCF	chr3:47128956-47129006	GM13977	blood:	n/a	n/a
49	CTCF	chr3:47128908-47129051	GM12891	blood:	n/a	n/a
50	CTCF	chr3:47128900-47129050	Caco-2	colon:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:47164794-47164844	AoSMC	blood vessel:	n/a
2	chr3:47165568-47165618	HRE	kidney:	n/a
3	chr3:47168872-47168922	SKMC	muscle:	n/a
4	chr3:47165568-47165618	Hepatocyte	liver:	n/a
5	chr3:47156062-47156112	HRCEpiC	kidney:	n/a
6	chr3:47156062-47156112	HRPEpiC	eye:	n/a
7	chr3:47149884-47149934	NH-A	brain:	n/a
8	chr3:47165568-47165618	AG04449	skin:	fetal
9	chr3:47164921-47164971	K562	blood:	n/a
10	chr3:47164921-47164971	T-47D	breast:	n/a
11	chr3:47156062-47156112	ProgFib	skin:	n/a
12	chr3:47138673-47138723	SK-N-MC	brain:	n/a
13	chr3:47149884-47149934	HNPCEpiC	eye:	n/a
14	chr3:47164921-47164971	ECC-1	luminal epithelium:	n/a
15	chr3:47156062-47156112	HepG2	liver:	n/a
16	chr3:47164804-47164854	NHBE	bronchial:	n/a
17	chr3:47164921-47164971	PFSK-1	brain:	n/a
18	chr3:47156062-47156112	SK-N-MC	brain:	n/a
19	chr3:47164921-47164971	HRPEpiC	eye:	n/a
20	chr3:47168872-47168922	MCF10A-Er-Src	breast:	n/a
21	chr3:47164794-47164844	AG09309	skin:	n/a
22	chr3:47165568-47165618	GM19239	blood:	n/a
23	chr3:47156062-47156112	K562	blood:	n/a
24	chr3:47156062-47156112	HPAEpiC	pulmonary alveolar:	n/a
25	chr3:47165568-47165618	BE2_C	brain:	n/a
26	chr3:47149884-47149934	AoSMC	blood vessel:	n/a
27	chr3:47165568-47165618	SK-N-MC	brain:	n/a
28	chr3:47168872-47168922	LNCaP	prostate:	n/a
29	chr3:47164804-47164854	HRE	kidney:	n/a
30	chr3:47156062-47156112	AG04450	lung:	fetal
31	chr3:47164794-47164844	SKMC	muscle:	n/a
32	chr3:47156062-47156112	HRE	kidney:	n/a
33	chr3:47164804-47164854	HL-60	blood:	n/a
34	chr3:47168872-47168922	HRCEpiC	kidney:	n/a
35	chr3:47165568-47165618	K562	blood:	n/a
36	chr3:47156062-47156112	BJ	skin:	n/a
37	chr3:47164921-47164971	SK-N-SH_RA	brain:	n/a
38	chr3:47164804-47164854	BE2_C	brain:	n/a
39	chr3:47164921-47164971	HRCEpiC	kidney:	n/a
40	chr3:47164794-47164844	HRCEpiC	kidney:	n/a
41	chr3:47165568-47165618	HPAEpiC	pulmonary alveolar:	n/a
42	chr3:47164794-47164844	SK-N-SH	brain:	n/a
43	chr3:47138673-47138723	HIPEpiC	eye:	n/a
44	chr3:47165568-47165618	NHDF-neo	bronchial:	n/a
45	chr3:47164804-47164854	HAEpiC	amniotic membrane:	n/a
46	chr3:47164921-47164971	Caco-2	colon:	n/a
47	chr3:47138673-47138723	MCF-7	breast:	n/a
48	chr3:47164804-47164854	AoSMC	blood vessel:	n/a
49	chr3:47138673-47138723	HEEpiC	esophagus:	n/a
50	chr3:47138673-47138723	SKMC	muscle:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:47125477..47129323-chr3:47137612..47139651,3	K562	blood:
2	chr3:47122254..47124275-chr3:47192922..47194900,2	K562	blood:
3	chr3:47125477..47129323-chr3:47137612..47139651,3	K562	blood:
4	chr3:47137775..47140078-chr3:47143848..47146629,2	MCF-7	breast:
5	chr3:47169888..47172250-chr3:47173863..47176112,2	K562	blood:
6	chr3:47160235..47164319-chr3:47167866..47171765,6	K562	blood:
7	chr3:47151756..47154654-chr3:47157875..47159694,2	K562	blood:
8	chr3:47121965..47124709-chr3:47429013..47430772,2	K562	blood:
9	chr3:47147445..47150358-chr3:47462787..47464363,2	K562	blood:
10	chr3:47122352..47125407-chr3:47126462..47130249,3	K562	blood:
11	chr3:47160235..47164319-chr3:47167866..47171765,6	K562	blood:
12	chr3:47164535..47167910-chr3:47168833..47170750,3	K562	blood:
13	chr3:47150417..47152283-chr3:47160822..47163333,2	MCF-7	breast:
14	chr3:47117444..47119975-chr3:47141387..47143617,2	K562	blood:
15	chr3:47132552..47135430-chr4:99181740..99183260,2	MCF-7	breast:
16	chr3:47157453..47160237-chr3:47204049..47206459,2	K562	blood:
17	chr3:47150626..47153559-chr3:47155579..47157656,2	K562	blood:
18	chr3:47170479..47172359-chr3:47184922..47186502,2	K562	blood:
19	chr3:47115603..47117354-chr3:47121967..47124210,2	K562	blood:
20	chr3:47139097..47140627-chr3:47822792..47824576,2	K562	blood:
21	chr3:47148587..47150185-chr3:47152146..47155145,2	K562	blood:
22	chr3:47145721..47147823-chr3:47174346..47176792,2	K562	blood:
23	chr3:47148587..47150185-chr3:47152146..47155145,2	K562	blood:
24	chr3:47144584..47146288-chr3:47160200..47162965,2	K562	blood:
25	chr3:47150626..47153559-chr3:47155579..47157656,2	K562	blood:
26	chr3:47157859..47160237-chr3:47204049..47206220,2	K562	blood:
27	chr3:47160775..47162844-chr3:47166336..47168539,2	MCF-7	breast:
28	chr3:47160775..47162844-chr3:47166336..47168539,2	MCF-7	breast:
29	chr3:47150417..47152283-chr3:47160822..47163333,2	MCF-7	breast:
30	chr3:47118002..47122103-chr3:47123133..47127114,5	K562	blood:
31	chr3:47144386..47146568-chr3:47206115..47208943,2	K562	blood:
32	chr3:47016641..47019456-chr3:47138519..47140806,2	K562	blood:
33	chr3:47160419..47162941-chr3:47203566..47205231,2	K562	blood:
34	chr3:47144584..47146288-chr3:47160200..47162965,2	K562	blood:
35	chr3:47124271..47126877-chr3:47134928..47137579,2	K562	blood:
36	chr3:47160899..47162845-chr3:47163476..47165450,2	K562	blood:
37	chr3:47151756..47154654-chr3:47157875..47159694,2	K562	blood:
38	chr3:47098199..47100265-chr3:47118377..47121357,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000251938	TF binding region
SETD2	TF binding region
ENSG00000251938	CpG island
SETD2	CpG island
ENSG00000160799	chromatin interactions
ENSG00000173473	chromatin interactions
ENSG00000214559	chromatin interactions
ENSG00000227398	chromatin interactions
ENSG00000114650	chromatin interactions
ENSG00000138698	chromatin interactions
ENSG00000251938	chromatin interactions
ENSG00000181555	chromatin interactions

Extended variants
information (count: 1700 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:1700 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142740299	chr3:47120597-47120598	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs186066749	chr3:47120610-47120611	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs7433300	chr3:47120640-47120641	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs532355303	chr3:47120676-47120677	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs547567253	chr3:47120694-47120695	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs559732307	chr3:47120850-47120851	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs530008421	chr3:47120890-47120891	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs565083492	chr3:47120920-47120921	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs190884272	chr3:47120927-47120928	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs183429105	chr3:47120928-47120929	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs375751063	chr3:47120954-47120955	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs537014766	chr3:47121013-47121014	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs552005769	chr3:47121087-47121088	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs6414435	chr3:47121140-47121141	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs534894471	chr3:47121157-47121158	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs187764825	chr3:47121186-47121187	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs191963673	chr3:47121202-47121203	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs200926623	chr3:47121232-47121233	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs550915272	chr3:47121263-47121264	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs183494823	chr3:47121273-47121274	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs558299556	chr3:47121278-47121279	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs147387792	chr3:47121294-47121295	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs114818993	chr3:47121339-47121340	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs372909488	chr3:47121360-47121361	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs7641068	chr3:47121394-47121395	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs557980266	chr3:47121439-47121440	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs573365780	chr3:47121474-47121475	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs377229866	chr3:47121478-47121479	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs544080109	chr3:47121539-47121540	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs559565443	chr3:47121560-47121561	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs530049993	chr3:47121606-47121607	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs139445937	chr3:47121622-47121623	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs368693668	chr3:47121627-47121628	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs532541901	chr3:47121639-47121640	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs149470529	chr3:47121665-47121666	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs530424793	chr3:47121681-47121682	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs529937470	chr3:47121771-47121772	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs143875847	chr3:47121782-47121783	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs570261773	chr3:47121824-47121825	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs528154384	chr3:47121861-47121862	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs546827151	chr3:47121872-47121873	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs73831474	chr3:47121901-47121902	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs371430721	chr3:47121902-47121903	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs142230690	chr3:47121911-47121912	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs375753290	chr3:47121912-47121913	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs188198433	chr3:47121972-47121973	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs552336961	chr3:47122040-47122041	Strong transcription Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs539490511	chr3:47122044-47122045	Strong transcription Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs558129066	chr3:47122273-47122274	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs34406148	chr3:47122300-47122301	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	21080181	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Kartagener syndrome	16639409	CNVD
Biliary cancer	19435499	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Breast cancer	21509527	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22032731	CNVD
Non-small cell lung cancer	20864512	CNVD
Colorectal cancer	16912164	CNVD
Non-small cell lung cancer	19010865	CNVD
Colorectal cancer	16272173	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute myeloid leukemia	17268525	CNVD
Salivary gland tumor	18059337	CNVD
Gastric cancer	16891809	CNVD
Night blindness	17160897	CNVD
Cancer	17160897	CNVD
Breast cancer	20409316	CNVD
Lung cancer	17297452	CNVD
Multiple myeloma	16616336	CNVD
Effusion lymphoma	18079361	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Urothelial cell carcinoma	18451213	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Melanoma	17363583	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Adrenocortical carcinoma	18281524	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1890 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:47078000-47130600	Weak transcription	Stomach Mucosa	stomach
2	chr3:47079600-47123800	Weak transcription	Pancreas	Pancrea
3	chr3:47079600-47124200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr3:47079800-47124200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr3:47083200-47135200	Weak transcription	Small Intestine	intestine
6	chr3:47083400-47138600	Weak transcription	Psoas Muscle	Psoas
7	chr3:47093400-47122600	Strong transcription	Monocytes-CD14+_RO01746	blood
8	chr3:47093800-47123400	Strong transcription	Primary monocytes fromperipheralblood	blood
9	chr3:47094200-47123800	Weak transcription	Esophagus	oesophagus
10	chr3:47095800-47121000	Weak transcription	Fetal Brain Male	brain
11	chr3:47098800-47121800	Weak transcription	Rectal Smooth Muscle	rectum
12	chr3:47098800-47122000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr3:47098800-47122000	Weak transcription	Aorta	Aorta
14	chr3:47098800-47149600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr3:47099000-47121600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr3:47099000-47121800	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr3:47099000-47121800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr3:47099000-47121800	Weak transcription	Skeletal Muscle Male	skeletal muscle
19	chr3:47099000-47122000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr3:47099000-47122000	Weak transcription	Gastric	stomach
21	chr3:47099000-47125200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr3:47099000-47128200	Weak transcription	Spleen	Spleen
23	chr3:47099200-47122000	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr3:47100000-47122200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr3:47101000-47125200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr3:47101200-47123800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
27	chr3:47101400-47147800	Strong transcription	Dnd41	blood
28	chr3:47101600-47123800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr3:47101800-47121800	Weak transcription	Stomach Smooth Muscle	stomach
30	chr3:47103800-47122000	Weak transcription	Placenta Amnion	Placenta Amnion
31	chr3:47105000-47121800	Weak transcription	HMEC	breast
32	chr3:47106200-47121800	Weak transcription	Cortex derived primary cultured neurospheres	brain
33	chr3:47106800-47121600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
34	chr3:47106800-47121600	Weak transcription	Colon Smooth Muscle	Colon
35	chr3:47107000-47121800	Weak transcription	H1 Cell Line	embryonic stem cell
36	chr3:47107600-47122000	Weak transcription	Ovary	ovary
37	chr3:47107800-47121600	Weak transcription	Duodenum Smooth Muscle	Duodenum
38	chr3:47108000-47121800	Weak transcription	Brain Germinal Matrix	brain
39	chr3:47108000-47121800	Weak transcription	Colonic Mucosa	Colon
40	chr3:47108000-47122000	Weak transcription	Lung	lung
41	chr3:47108000-47125000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr3:47108200-47121400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
43	chr3:47110200-47150200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr3:47110400-47133200	Strong transcription	Primary T cells fromperipheralblood	blood
45	chr3:47110600-47131600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
46	chr3:47110600-47148000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
47	chr3:47110800-47125200	Strong transcription	Primary B cells from peripheral blood	blood
48	chr3:47111000-47147600	Strong transcription	Primary T helper cells fromperipheralblood	blood
49	chr3:47111800-47132400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr3:47112400-47153600	Weak transcription	Pancreatic Islets	Pancreatic Islet

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