Variant report

Variant	nsv526359
Chromosome Location	chr2:57616965-57703467
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:363)
CpG islands
(count:61)
Chromatin interactive
region (count:16)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:363 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr2:57677308-57677677	GM12878	blood:	n/a	n/a
2	ATF2	chr2:57677283-57677736	GM12878	blood:	n/a	n/a
3	BACH1	chr2:57623493-57623938	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr2:57677301-57677735	GM12878	blood:	n/a	n/a
5	BATF	chr2:57677353-57677672	GM12878	blood:	n/a	n/a
6	BCL11A	chr2:57677351-57677642	GM12878	blood:	n/a	n/a
7	BCL11A	chr2:57677323-57677668	GM12878	blood:	n/a	n/a
8	BCL3	chr2:57656947-57657199	GM12878	blood:	n/a	n/a
9	BCL3	chr2:57677288-57677769	GM12878	blood:	n/a	n/a
10	BHLHE40	chr2:57677398-57677689	GM12878	blood:	n/a	n/a
11	BRCA1	chr2:57625938-57625986	GM12878	blood:	n/a	n/a
12	CEBPB	chr2:57644218-57644262	A549	lung:	n/a	n/a
13	CEBPB	chr2:57686957-57687253	A549	lung:	n/a	chr2:57687072-57687083
14	CEBPB	chr2:57695207-57695482	A549	lung:	n/a	chr2:57695337-57695348
15	CEBPB	chr2:57695187-57695496	IMR90	lung:	n/a	chr2:57695337-57695348
16	CEBPB	chr2:57671064-57671644	HCT-116	colon:	n/a	chr2:57671434-57671445
17	CEBPB	chr2:57630938-57631021	A549	lung:	n/a	chr2:57630962-57630975
18	CEBPB	chr2:57695169-57695487	HepG2	liver:	n/a	chr2:57695337-57695348
19	CEBPB	chr2:57686952-57687247	HepG2	liver:	n/a	chr2:57687072-57687083
20	CEBPB	chr2:57671281-57671572	HepG2	liver:	n/a	chr2:57671434-57671445
21	CEBPB	chr2:57653300-57653715	HepG2	liver:	n/a	n/a
22	CEBPB	chr2:57635068-57635356	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr2:57671313-57671586	IMR90	lung:	n/a	chr2:57671434-57671445
24	CEBPB	chr2:57670883-57671690	HCT-116	colon:	n/a	chr2:57671434-57671445
25	CEBPB	chr2:57677243-57677819	GM12878	blood:	n/a	n/a
26	CEBPB	chr2:57671275-57671658	A549	lung:	n/a	chr2:57671434-57671445
27	CEBPB	chr2:57671256-57671580	Hela-S3	cervix:	n/a	chr2:57671434-57671445
28	CHD2	chr2:57677410-57677610	GM12878	blood:	n/a	n/a
29	CREB1	chr2:57677261-57677817	GM12878	blood:	n/a	n/a
30	CTCF	chr2:57681180-57681330	NHEK	skin:	n/a	n/a
31	CTCF	chr2:57625791-57625901	MCF-7	breast:	n/a	n/a
32	CTCF	chr2:57681160-57681310	GM12866	blood:	n/a	n/a
33	CTCF	chr2:57681140-57681290	RPTEC	kidney:	n/a	n/a
34	CTCF	chr2:57686076-57686166	GM20000	blood:	n/a	n/a
35	CTCF	chr2:57681216-57681320	GM13977	blood:	n/a	n/a
36	CTCF	chr2:57681200-57681350	HepG2	liver:	n/a	n/a
37	CTCF	chr2:57681180-57681330	Caco-2	colon:	n/a	n/a
38	CTCF	chr2:57681260-57681410	BE2_C	brain:	n/a	n/a
39	CTCF	chr2:57681160-57681310	GM12872	blood:	n/a	n/a
40	CTCF	chr2:57681200-57681350	HEK293	kidney:	n/a	n/a
41	CTCF	chr2:57625805-57625897	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr2:57681220-57681370	HCPEpiC	choroid plexus:	n/a	n/a
43	CTCF	chr2:57681140-57681290	GM12872	blood:	n/a	n/a
44	CTCF	chr2:57700160-57700310	AG10803	skin:	n/a	n/a
45	CTCF	chr2:57681172-57681356	HUVEC	blood vessel:	n/a	n/a
46	CTCF	chr2:57681180-57681330	HCPEpiC	choroid plexus:	n/a	n/a
47	CTCF	chr2:57681140-57681290	GM12873	blood:	n/a	n/a
48	CTCF	chr2:57681420-57681570	GM12871	blood:	n/a	n/a
49	CTCF	chr2:57681180-57681330	GM12864	blood:	n/a	n/a
50	CTCF	chr2:57681160-57681310	GM12867	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:57634837-57634887	HPAEpiC	pulmonary alveolar:	n/a
2	chr2:57634837-57634887	HMEC	breast:	n/a
3	chr2:57634837-57634887	SAEC	small airway:	n/a
4	chr2:57634837-57634887	Hela-S3	cervix:	n/a
5	chr2:57634837-57634887	HUVEC	blood vessel:	n/a
6	chr2:57634837-57634887	AG09319	gingival:	n/a
7	chr2:57634837-57634887	GM06990	blood:	n/a
8	chr2:57634837-57634887	ProgFib	skin:	n/a
9	chr2:57634837-57634887	AG09309	skin:	n/a
10	chr2:57634837-57634887	HCPEpiC	choroid plexus:	n/a
11	chr2:57634837-57634887	GM19239	blood:	n/a
12	chr2:57634837-57634887	HepG2	liver:	n/a
13	chr2:57634837-57634887	CMK	blood:	n/a
14	chr2:57634837-57634887	NB4	blood:	n/a
15	chr2:57634837-57634887	AG04450	lung:	fetal
16	chr2:57634837-57634887	SKMC	muscle:	n/a
17	chr2:57634837-57634887	HEEpiC	esophagus:	n/a
18	chr2:57634837-57634887	ECC-1	luminal epithelium:	n/a
19	chr2:57634837-57634887	NHBE	bronchial:	n/a
20	chr2:57634837-57634887	PANC-1	pancreas:	n/a
21	chr2:57634837-57634887	SK-N-SH	brain:	n/a
22	chr2:57634837-57634887	HL-60	blood:	n/a
23	chr2:57634837-57634887	K562	blood:	n/a
24	chr2:57634837-57634887	SK-N-SH_RA	brain:	n/a
25	chr2:57634837-57634887	MCF10A-Er-Src	breast:	n/a
26	chr2:57634837-57634887	Caco-2	colon:	n/a
27	chr2:57634837-57634887	AG04449	skin:	fetal
28	chr2:57634837-57634887	HRCEpiC	kidney:	n/a
29	chr2:57634837-57634887	LNCaP	prostate:	n/a
30	chr2:57634837-57634887	Jurkat	blood:	n/a
31	chr2:57634837-57634887	HCM	heart:	n/a
32	chr2:57634837-57634887	AG10803	skin:	n/a
33	chr2:57634837-57634887	HAEpiC	amniotic membrane:	n/a
34	chr2:57634837-57634887	MCF-7	breast:	n/a
35	chr2:57634837-57634887	HCT-116	colon:	n/a
36	chr2:57634837-57634887	PFSK-1	brain:	n/a
37	chr2:57634837-57634887	ovcar-3	ovarian:	n/a
38	chr2:57634837-57634887	HCF	heart:	n/a
39	chr2:57634837-57634887	RPTEC	kidney:	n/a
40	chr2:57634837-57634887	A549	lung:	n/a
41	chr2:57634837-57634887	GM12892	blood:	n/a
42	chr2:57634837-57634887	NT2-D1	testis:	n/a
43	chr2:57634837-57634887	HRPEpiC	eye:	n/a
44	chr2:57634837-57634887	HNPCEpiC	eye:	n/a
45	chr2:57634837-57634887	H1-hESC	embryonic stem cell:	embryo
46	chr2:57634837-57634887	IMR90	lung:	fetal
47	chr2:57634837-57634887	NH-A	brain:	n/a
48	chr2:57634837-57634887	T-47D	breast:	n/a
49	chr2:57634837-57634887	SK-N-MC	brain:	n/a
50	chr2:57634837-57634887	BJ	skin:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:57669021..57671005-chr2:57673900..57675904,2	K562	blood:
2	chr2:57695038..57697832-chr2:57697917..57700071,2	MCF-7	breast:
3	chr2:57680802..57681722-chr2:57724395..57725159,3	MCF-7	breast:
4	chr2:57669021..57671005-chr2:57673900..57675904,2	K562	blood:
5	chr2:57633446..57635721-chr2:57643662..57645382,2	MCF-7	breast:
6	chr2:57696000..57698302-chr2:57699957..57702610,2	K562	blood:
7	chr2:57627476..57629537-chr2:57644280..57646195,2	MCF-7	breast:
8	chr2:57670502..57672263-chr2:57675373..57678104,2	MCF-7	breast:
9	chr2:57686552..57689405-chr2:57735534..57737911,2	K562	blood:
10	chr2:57695038..57697832-chr2:57697917..57700071,2	MCF-7	breast:
11	chr2:57631506..57633055-chr2:57645760..57647304,2	MCF-7	breast:
12	chr2:57670502..57672263-chr2:57675373..57678104,2	MCF-7	breast:
13	chr2:57633446..57635721-chr2:57643662..57645382,2	MCF-7	breast:
14	chr2:57627476..57629537-chr2:57644280..57646195,2	MCF-7	breast:
15	chr2:57696000..57698302-chr2:57699957..57702610,2	K562	blood:
16	chr2:57631506..57633055-chr2:57645760..57647304,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FANCL-8	chr2:57657781-57657828	NONHSAT070833
2	lnc-VRK2-16	chr2:57659475-57659520	NONHSAT070834
3	lnc-FANCL-8	chr2:57657275-57657340	NONHSAT070833
4	lnc-FANCL-8	chr2:57656683-57656947	NONHSAT070833
5	lnc-VRK2-16	chr2:57672949-57673194	NONHSAT070834

No data

Variant related genes	Relation type
ENSG00000270569	TF binding region
ENSG00000270569	CpG island

Extended variants
information (count: 1900 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:1900 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571895820	chr2:57623212-57623213	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs75046815	chr2:57623231-57623232	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs1607429	chr2:57623240-57623241	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs567720852	chr2:57623331-57623332	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs536652847	chr2:57623334-57623335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs556327842	chr2:57623374-57623375	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs76675973	chr2:57623378-57623379	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs570186483	chr2:57623399-57623400	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs545003571	chr2:57623433-57623434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs367714495	chr2:57623478-57623479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs144773053	chr2:57623517-57623518	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs371671179	chr2:57623520-57623521	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs540787205	chr2:57623531-57623532	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs538623469	chr2:57623549-57623550	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs560654999	chr2:57623550-57623551	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs558449649	chr2:57623555-57623556	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs181340709	chr2:57623558-57623559	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs139715990	chr2:57623584-57623585	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs543496185	chr2:57623671-57623672	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs114804163	chr2:57623695-57623696	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs532109366	chr2:57623711-57623712	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs185815343	chr2:57623729-57623730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs144466989	chr2:57623741-57623742	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs527894315	chr2:57623767-57623768	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs547964084	chr2:57623771-57623772	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs572380005	chr2:57623779-57623780	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs190573247	chr2:57623785-57623786	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs536385511	chr2:57623822-57623823	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs10170749	chr2:57623850-57623851	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs569973876	chr2:57623891-57623892	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs538991344	chr2:57623919-57623920	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs558439411	chr2:57623945-57623946	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs181494699	chr2:57623950-57623951	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs367898331	chr2:57623966-57623967	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs146155232	chr2:57624027-57624028	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs554386186	chr2:57624041-57624042	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs372128311	chr2:57624053-57624054	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs140206742	chr2:57624067-57624068	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs543178351	chr2:57624086-57624087	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs563365886	chr2:57624089-57624090	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs532023984	chr2:57624097-57624098	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs545772956	chr2:57624104-57624105	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs142269470	chr2:57624118-57624119	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs151257372	chr2:57624124-57624125	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs186187093	chr2:57624132-57624133	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs10179366	chr2:57624133-57624134	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs561357732	chr2:57624141-57624142	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs117154297	chr2:57624164-57624165	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs550022112	chr2:57624269-57624270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs192110875	chr2:57624277-57624278	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	16272173	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Retinoblastoma	22278416	CNVD
Cancer	21183584	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Hereditary non-polyposis colorectal cancer	19566914	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Mental retardation	19951919	CNVD
Myelofibrosis	22110671	CNVD
Microcephaly	20799320	CNVD
camptodactyly	20799320	CNVD
cognitive delay	20799320	CNVD
prenatal and postnatal growth deficiency	20799320	CNVD
ptosis of eyelids	20799320	CNVD
Maculopathy	20981449	CNVD
2p16.1 microdeletion syndrome	22283845	CNVD
Autism	22579565	CNVD
Autism	16963482	CNVD
Autism	21750575	CNVD
idiopathic intellectual disability	16963482	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Multiple myeloma	16616336	CNVD
Follicular lymphoma	17699855	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:106 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:57623200-57624000	Enhancers	Primary hematopoietic stem cells short term culture	blood
2	chr2:57623400-57623800	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr2:57623400-57624000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr2:57623400-57624200	Enhancers	H1 Cell Line	embryonic stem cell
5	chr2:57623400-57624200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr2:57623400-57624200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr2:57623400-57624200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr2:57623400-57624200	Enhancers	A549	lung
9	chr2:57623400-57624200	Enhancers	Monocytes-CD14+_RO01746	blood
10	chr2:57623400-57624400	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr2:57623600-57624000	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr2:57623800-57624000	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr2:57623800-57625000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr2:57623800-57625200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr2:57624000-57624200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
16	chr2:57624000-57634800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr2:57624200-57624800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr2:57624800-57625400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr2:57625000-57625200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr2:57629000-57629400	Enhancers	Fetal Brain Female	brain
21	chr2:57629000-57630400	Enhancers	Fetal Lung	lung
22	chr2:57633400-57633600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr2:57633400-57636000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr2:57633600-57633800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr2:57633800-57634800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr2:57634200-57636000	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr2:57634400-57635800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
28	chr2:57634600-57635200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr2:57634600-57635600	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr2:57634600-57635800	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr2:57634600-57636000	Enhancers	H1 Cell Line	embryonic stem cell
32	chr2:57634600-57636000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr2:57634800-57635200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr2:57634800-57635200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
35	chr2:57634800-57635400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr2:57634800-57635600	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr2:57634800-57635800	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr2:57634800-57635800	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr2:57634800-57635800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr2:57634800-57636000	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr2:57635000-57635400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr2:57635000-57635400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr2:57635000-57635400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr2:57635400-57637600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr2:57644200-57644400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr2:57645400-57645800	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr2:57645800-57646200	Active TSS	HUES6 Cell Line	embryonic stem cell
48	chr2:57645800-57646400	Active TSS	ES-I3 Cell Line	embryonic stem cell
49	chr2:57654800-57655200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr2:57656400-57658000	Enhancers	Monocytes-CD14+_RO01746	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links