Variant report

Variant	nsv2834
Chromosome Location	chr2:96772925-96785110
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	chr2:96782951-96783012	HepG2	liver:	n/a	n/a
2	ATF3	chr2:96782739-96783021	HepG2	liver:	n/a	n/a
3	ATF3	chr2:96777584-96777802	K562	blood:	n/a	n/a
4	BACH1	chr2:96774128-96774400	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr2:96781886-96783188	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr2:96783420-96783795	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL3	chr2:96781533-96781896	GM12878	blood:	n/a	n/a
8	BCLAF1	chr2:96782646-96783121	GM12878	blood:	n/a	chr2:96782920-96782933 chr2:96782912-96782925
9	BHLHE40	chr2:96782759-96783267	K562	blood:	n/a	chr2:96782901-96782917 chr2:96782912-96782928
10	BHLHE40	chr2:96783680-96783861	K562	blood:	n/a	n/a
11	BHLHE40	chr2:96777171-96777276	GM12878	blood:	n/a	n/a
12	BHLHE40	chr2:96777144-96777217	K562	blood:	n/a	n/a
13	BRCA1	chr2:96782730-96783019	H1-hESC	embryonic stem cell:	n/a	n/a
14	BRCA1	chr2:96782874-96783038	HepG2	liver:	n/a	n/a
15	CCNT2	chr2:96782166-96783194	K562	blood:	n/a	chr2:96782722-96782731
16	CEBPB	chr2:96778550-96778851	Hela-S3	cervix:	n/a	chr2:96778689-96778700
17	CEBPB	chr2:96778513-96778882	A549	lung:	n/a	chr2:96778689-96778700
18	CEBPB	chr2:96785081-96785445	K562	blood:	n/a	chr2:96785258-96785269
19	CEBPB	chr2:96778523-96778881	HepG2	liver:	n/a	chr2:96778689-96778700
20	CEBPB	chr2:96778593-96778832	IMR90	lung:	n/a	chr2:96778689-96778700
21	CEBPB	chr2:96778583-96778871	K562	blood:	n/a	chr2:96778689-96778700
22	CEBPB	chr2:96785109-96785438	HepG2	liver:	n/a	chr2:96785258-96785269
23	CEBPB	chr2:96778521-96778831	H1-hESC	embryonic stem cell:	n/a	chr2:96778689-96778700
24	CEBPB	chr2:96782793-96783075	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr2:96774132-96774799	H1-hESC	embryonic stem cell:	n/a	chr2:96774471-96774481
26	CHD2	chr2:96782980-96783161	K562	blood:	n/a	n/a
27	CHD2	chr2:96782368-96782490	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr2:96782713-96783107	GM12878	blood:	n/a	chr2:96782875-96782885
29	CHD2	chr2:96782742-96783092	HepG2	liver:	n/a	chr2:96782875-96782885
30	CHD2	chr2:96773921-96773940	HepG2	liver:	n/a	n/a
31	CHD2	chr2:96783403-96783562	HepG2	liver:	n/a	n/a
32	CREB1	chr2:96782672-96783073	A549	lung:	n/a	n/a
33	CTBP2	chr2:96773011-96774966	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTBP2	chr2:96781457-96783861	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr2:96779160-96779310	HEK293	kidney:	n/a	n/a
36	CTCF	chr2:96783680-96783830	WERI-Rb-1	eye:	n/a	chr2:96783740-96783753
37	CTCF	chr2:96783720-96783870	GM12864	blood:	n/a	chr2:96783740-96783753
38	CTCF	chr2:96783540-96783690	HRPEpiC	eye:	n/a	chr2:96783645-96783653
39	CTCF	chr2:96783145-96783235	GM19239	blood:	n/a	n/a
40	CTCF	chr2:96782860-96783010	HA-sp	spinal cord:	n/a	chr2:96782905-96782918 chr2:96782904-96782920 chr2:96782906-96782916 chr2:96782903-96782921
41	CTCF	chr2:96778967-96779452	K562	blood:	n/a	n/a
42	CTCF	chr2:96782900-96783050	HCFaa	heart:	n/a	chr2:96782905-96782918 chr2:96782904-96782920 chr2:96782906-96782916 chr2:96782903-96782921
43	CTCF	chr2:96782734-96783130	GM12891	blood:	n/a	chr2:96782905-96782918 chr2:96782904-96782920 chr2:96782906-96782916 chr2:96782903-96782921
44	CTCF	chr2:96783680-96783830	HRE	kidney:	n/a	chr2:96783740-96783753
45	CTCF	chr2:96783680-96783830	GM12871	blood:	n/a	chr2:96783740-96783753
46	CTCF	chr2:96782646-96783108	HepG2	liver:	n/a	chr2:96782905-96782918 chr2:96782904-96782920 chr2:96782906-96782916 chr2:96782903-96782921
47	CTCF	chr2:96782769-96783043	Pancreas_OC	pancreas:	n/a	chr2:96782905-96782918 chr2:96782904-96782920 chr2:96782906-96782916 chr2:96782903-96782921
48	CTCF	chr2:96783680-96783830	GM06990	blood:	n/a	chr2:96783740-96783753
49	CTCF	chr2:96783640-96783790	HCT-116	colon:	n/a	chr2:96783645-96783653 chr2:96783740-96783753
50	CTCF	chr2:96779219-96779368	GM10266	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:96780804-96780854	GM12878	blood:	n/a
2	chr2:96782027-96782077	NH-A	brain:	n/a
3	chr2:96783070-96783120	NHBE	bronchial:	n/a
4	chr2:96780594-96780644	LNCaP	prostate:	n/a
5	chr2:96780655-96780705	PFSK-1	brain:	n/a
6	chr2:96780804-96780854	GM12891	blood:	n/a
7	chr2:96780594-96780644	HCF	heart:	n/a
8	chr2:96780804-96780854	HEEpiC	esophagus:	n/a
9	chr2:96780804-96780854	GM12892	blood:	n/a
10	chr2:96780655-96780705	HMEC	breast:	n/a
11	chr2:96781407-96781457	ProgFib	skin:	n/a
12	chr2:96781891-96781941	NB4	blood:	n/a
13	chr2:96779778-96779828	ECC-1	luminal epithelium:	n/a
14	chr2:96781407-96781457	A549	lung:	n/a
15	chr2:96780655-96780705	NT2-D1	testis:	n/a
16	chr2:96782027-96782077	LNCaP	prostate:	n/a
17	chr2:96774492-96774542	NHDF-neo	bronchial:	n/a
18	chr2:96781891-96781941	RPTEC	kidney:	n/a
19	chr2:96780594-96780644	HAEpiC	amniotic membrane:	n/a
20	chr2:96781407-96781457	PrEC	prostate:	n/a
21	chr2:96780804-96780854	AG04449	skin:	fetal
22	chr2:96782027-96782077	HIPEpiC	eye:	n/a
23	chr2:96781891-96781941	AG09309	skin:	n/a
24	chr2:96780804-96780854	HRE	kidney:	n/a
25	chr2:96782027-96782077	SAEC	small airway:	n/a
26	chr2:96783070-96783120	SKMC	muscle:	n/a
27	chr2:96782027-96782077	T-47D	breast:	n/a
28	chr2:96783070-96783120	HPAEpiC	pulmonary alveolar:	n/a
29	chr2:96782443-96782493	HPAEpiC	pulmonary alveolar:	n/a
30	chr2:96780655-96780705	HEEpiC	esophagus:	n/a
31	chr2:96783070-96783120	U87	brain:	n/a
32	chr2:96780804-96780854	HNPCEpiC	eye:	n/a
33	chr2:96778750-96778800	CMK	blood:	n/a
34	chr2:96774492-96774542	HIPEpiC	eye:	n/a
35	chr2:96780594-96780644	Hepatocyte	liver:	n/a
36	chr2:96779778-96779828	HRPEpiC	eye:	n/a
37	chr2:96783070-96783120	HRPEpiC	eye:	n/a
38	chr2:96781407-96781457	T-47D	breast:	n/a
39	chr2:96780655-96780705	NH-A	brain:	n/a
40	chr2:96783070-96783120	GM19239	blood:	n/a
41	chr2:96774492-96774542	SAEC	small airway:	n/a
42	chr2:96781891-96781941	HUVEC	blood vessel:	n/a
43	chr2:96780594-96780644	HNPCEpiC	eye:	n/a
44	chr2:96781407-96781457	BJ	skin:	n/a
45	chr2:96778750-96778800	MCF10A-Er-Src	breast:	n/a
46	chr2:96781407-96781457	ECC-1	luminal epithelium:	n/a
47	chr2:96780594-96780644	HMEC	breast:	n/a
48	chr2:96781407-96781457	Hela-S3	cervix:	n/a
49	chr2:96780594-96780644	BE2_C	brain:	n/a
50	chr2:96780655-96780705	Hela-S3	cervix:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:96781378..96786213-chr2:96808688..96812498,6	MCF-7	breast:
2	chr2:96782213..96784499-chr2:96930229..96931847,2	MCF-7	breast:
3	chr2:96781942..96784647-chr2:96809826..96814461,4	MCF-7	breast:
4	chr2:96784034..96786646-chr2:96786886..96788520,2	MCF-7	breast:
5	chr2:96753566..96754241-chr2:96782628..96783306,2	K562	blood:
6	chr2:96777558..96778246-chr2:96839972..96840755,3	MCF-7	breast:
7	chr2:96777756..96780230-chr2:96872542..96875164,2	MCF-7	breast:
8	chr2:96769361..96771911-chr2:96776985..96778762,2	K562	blood:
9	chr2:96784106..96786319-chr2:96789442..96791079,2	K562	blood:
10	chr2:96768848..96771320-chr2:96776985..96780678,4	K562	blood:
11	chr2:96770104..96776221-chr2:96777736..96784239,9	MCF-7	breast:
12	chr2:96781026..96783523-chr2:96872750..96874386,2	MCF-7	breast:
13	chr2:96756578..96759551-chr2:96774122..96776954,2	MCF-7	breast:
14	chr2:96783327..96784989-chr2:96786453..96788374,2	K562	blood:
15	chr2:96769737..96771522-chr2:96772870..96775346,2	MCF-7	breast:
16	chr2:96656483..96658831-chr2:96781728..96784486,2	K562	blood:
17	chr2:96749229..96750745-chr2:96772910..96775152,2	MCF-7	breast:
18	chr2:96776047..96778196-chr2:96780042..96782966,2	MCF-7	breast:
19	chr2:96782361..96784893-chr2:96801744..96803597,2	MCF-7	breast:
20	chr2:96762558..96765319-chr2:96774708..96776428,2	K562	blood:
21	chr2:96688443..96689089-chr2:96782413..96783451,3	MCF-7	breast:
22	chr2:96766427..96768591-chr2:96778243..96780408,2	K562	blood:

Variant related genes	Relation type
ADRA2B	TF binding region
ADRA2B	CpG island
ENSG00000188886	chromatin interactions
ENSG00000204685	chromatin interactions
ENSG00000222040	chromatin interactions
ENSG00000084090	chromatin interactions
ENSG00000228873	chromatin interactions
ENSG00000135956	chromatin interactions
ENSG00000158050	chromatin interactions
ENSG00000174501	chromatin interactions

Extended variants
information (count: 436 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:436 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536668198	chr2:96772928-96772929	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs76413681	chr2:96772950-96772951	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
3	rs147762479	chr2:96772957-96772958	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs534108481	chr2:96772992-96772993	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs548100819	chr2:96772994-96772995	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs562169759	chr2:96772999-96773000	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs140199278	chr2:96773101-96773102	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs187102198	chr2:96773149-96773150	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs570849074	chr2:96773200-96773201	Enhancers Bivalent Enhancer Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs559149093	chr2:96773223-96773224	Enhancers Bivalent Enhancer Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs539874933	chr2:96773265-96773266	Enhancers Bivalent Enhancer Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs550472297	chr2:96773314-96773315	Enhancers Bivalent Enhancer Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs570273619	chr2:96773362-96773363	Enhancers Bivalent Enhancer Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs536013720	chr2:96773404-96773405	Enhancers Bivalent Enhancer Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs190827962	chr2:96773450-96773451	Enhancers Bivalent Enhancer Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs553629322	chr2:96773525-96773526	Enhancers Bivalent Enhancer Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs566310137	chr2:96773556-96773557	Enhancers Bivalent Enhancer Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs150312599	chr2:96773559-96773560	Enhancers Bivalent Enhancer Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs553487114	chr2:96773560-96773561	Enhancers Bivalent Enhancer Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs181697436	chr2:96773568-96773569	Enhancers Bivalent Enhancer Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs56039027	chr2:96773601-96773602	Enhancers Genic enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs545419822	chr2:96773652-96773653	Enhancers Genic enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs556392483	chr2:96773769-96773770	Enhancers Genic enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs576264772	chr2:96773777-96773778	Enhancers Genic enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs541958111	chr2:96773856-96773857	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs78520341	chr2:96773932-96773933	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs62152962	chr2:96773950-96773951	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs541520600	chr2:96773971-96773972	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs138055513	chr2:96773987-96773988	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs149084522	chr2:96774009-96774010	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs550214120	chr2:96774157-96774158	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs13019188	chr2:96774199-96774200	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs529558448	chr2:96774216-96774217	Flanking Active TSS Enhancers Bivalent Enhancer Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs72825829	chr2:96774247-96774248	Flanking Active TSS Enhancers Bivalent Enhancer Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs566127352	chr2:96774250-96774251	Flanking Active TSS Enhancers Bivalent Enhancer Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs544927025	chr2:96774261-96774262	Flanking Active TSS Enhancers Bivalent Enhancer Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs534918136	chr2:96774299-96774300	Flanking Active TSS Enhancers Bivalent Enhancer Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs553425612	chr2:96774400-96774401	Flanking Active TSS Enhancers Bivalent Enhancer Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs186132328	chr2:96774480-96774481	Flanking Active TSS Enhancers Bivalent Enhancer Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs35033714	chr2:96774650-96774651	Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs574904345	chr2:96774687-96774688	Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs539009388	chr2:96774745-96774746	Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs10183151	chr2:96774786-96774787	Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs576031582	chr2:96774795-96774796	Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs541746430	chr2:96774806-96774807	Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs555666854	chr2:96774823-96774824	Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs372616417	chr2:96774944-96774945	Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs58377194	chr2:96774978-96774979	Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs7561198	chr2:96774981-96774982	Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs564537315	chr2:96774987-96774988	Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:51)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	17483303	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Lung cancer	18438408	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Neuroblastoma	18574593	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21509527	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Epilepsy	22083797	CNVD
Glioblastoma multiforme	21138945	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:592 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:96769600-96773400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr2:96769800-96773000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr2:96770600-96773400	Weak transcription	Right Ventricle	heart
4	chr2:96770600-96774000	Weak transcription	Right Atrium	heart
5	chr2:96770800-96773200	Weak transcription	Left Ventricle	heart
6	chr2:96770800-96773600	Weak transcription	Fetal Heart	heart
7	chr2:96771600-96773200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr2:96772000-96773200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr2:96772000-96774000	Weak transcription	Spleen	Spleen
10	chr2:96772000-96782200	Weak transcription	Liver	Liver
11	chr2:96772800-96773000	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr2:96772800-96773400	Enhancers	Skeletal Muscle Male	skeletal muscle
13	chr2:96772800-96774400	Enhancers	Fetal Muscle Trunk	muscle
14	chr2:96772800-96774800	Enhancers	Duodenum Smooth Muscle	Duodenum
15	chr2:96772800-96774800	Enhancers	Fetal Muscle Leg	muscle
16	chr2:96773000-96773600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr2:96773000-96773800	Enhancers	HepG2	liver
18	chr2:96773000-96775400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr2:96773200-96773400	Bivalent Enhancer	Stomach Mucosa	stomach
20	chr2:96773200-96773600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr2:96773200-96774000	Enhancers	Primary hematopoietic stem cells	blood
22	chr2:96773200-96774200	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr2:96773200-96774400	Enhancers	Gastric	stomach
24	chr2:96773200-96774600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr2:96773200-96775600	Enhancers	H1 Cell Line	embryonic stem cell
26	chr2:96773200-96775600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr2:96773200-96775600	Enhancers	Left Ventricle	heart
28	chr2:96773200-96775800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr2:96773200-96776200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
30	chr2:96773400-96773600	Enhancers	Lung	lung
31	chr2:96773400-96773800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr2:96773400-96774400	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr2:96773400-96774800	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
34	chr2:96773400-96775400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr2:96773400-96776200	Enhancers	Right Ventricle	heart
36	chr2:96773600-96773800	Enhancers	Primary hematopoietic stem cells short term culture	blood
37	chr2:96773600-96774000	Enhancers	Fetal Thymus	thymus
38	chr2:96773600-96774200	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr2:96773600-96774200	Weak transcription	Lung	lung
40	chr2:96773600-96774600	Enhancers	Skeletal Muscle Female	skeletal muscle
41	chr2:96773600-96774600	Bivalent Enhancer	Stomach Smooth Muscle	stomach
42	chr2:96773600-96775200	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr2:96773600-96775400	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr2:96773600-96776200	Enhancers	Fetal Heart	heart
45	chr2:96773800-96774800	Flanking Active TSS	HepG2	liver
46	chr2:96773800-96775200	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr2:96773800-96775400	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr2:96773800-96775400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr2:96773800-96775600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr2:96773800-96775600	Enhancers	Placenta	Placenta

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