Variant report

Variant	nsv874197
Chromosome Location	chr2:57978858-58068741
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:654)
CpG islands
(count:305)
Chromatin interactive
region (count:14)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:654 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:57987011-57987296	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:58004102-58004565	K562	blood:	n/a	n/a
3	ATF2	chr2:58036295-58036793	GM12878	blood:	n/a	n/a
4	ATF2	chr2:58023548-58024173	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr2:58023643-58024051	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr2:58036301-58036756	GM12878	blood:	n/a	n/a
7	ATF2	chr2:57987004-57987361	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr2:57986897-57987440	A549	lung:	n/a	n/a
9	BATF	chr2:57987032-57987313	GM12878	blood:	n/a	n/a
10	BATF	chr2:57987544-57987875	GM12878	blood:	n/a	n/a
11	BATF	chr2:57987600-57987899	GM12878	blood:	n/a	n/a
12	BCL11A	chr2:58023700-58023881	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCL11A	chr2:58023688-58023959	H1-hESC	embryonic stem cell:	n/a	n/a
14	BCL3	chr2:57986988-57987518	A549	lung:	n/a	n/a
15	BCLAF1	chr2:58036584-58036924	GM12878	blood:	n/a	n/a
16	BCLAF1	chr2:57986905-57987354	GM12878	blood:	n/a	n/a
17	BHLHE40	chr2:57987004-57987358	GM12878	blood:	n/a	chr2:57987168-57987184
18	BHLHE40	chr2:57987037-57987376	K562	blood:	n/a	chr2:57987168-57987184
19	BRCA1	chr2:57987020-57987264	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr2:57987082-57987288	HepG2	liver:	n/a	n/a
21	CBX3	chr2:57986961-57987351	K562	blood:	n/a	n/a
22	CBX3	chr2:58025644-58026095	HCT-116	colon:	n/a	n/a
23	CCNT2	chr2:58003915-58004345	K562	blood:	n/a	chr2:58004252-58004272
24	CEBPB	chr2:58023708-58024097	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr2:57986953-57987329	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr2:57992915-57993112	HepG2	liver:	n/a	chr2:57993006-57993015 chr2:57993004-57993017 chr2:57993006-57993015 chr2:57993006-57993015
27	CEBPB	chr2:58047259-58047309	A549	lung:	n/a	n/a
28	CEBPB	chr2:58031044-58031333	HepG2	liver:	n/a	chr2:58031196-58031207 chr2:58031195-58031206 chr2:58031195-58031208
29	CEBPB	chr2:58047253-58047267	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPD	chr2:58003994-58004534	K562	blood:	n/a	n/a
31	CEBPD	chr2:58003956-58004557	K562	blood:	n/a	n/a
32	CHD1	chr2:57985974-57986064	GM12878	blood:	n/a	n/a
33	CHD1	chr2:58023946-58024228	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD1	chr2:57987084-57987426	GM12878	blood:	n/a	n/a
35	CHD2	chr2:57987032-57987329	Hela-S3	cervix:	n/a	n/a
36	CHD2	chr2:57986997-57987328	GM12878	blood:	n/a	n/a
37	CHD2	chr2:57987130-57987294	HepG2	liver:	n/a	n/a
38	CHD2	chr2:58023614-58024021	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr2:57987160-57987349	K562	blood:	n/a	n/a
40	CREB1	chr2:57987023-57987420	A549	lung:	n/a	n/a
41	CTCF	chr2:57987022-57987281	HepG2	liver:	n/a	chr2:57987138-57987154 chr2:57987142-57987150 chr2:57987137-57987155 chr2:57987139-57987160
42	CTCF	chr2:57987080-57987230	HCFaa	heart:	n/a	chr2:57987139-57987160 chr2:57987138-57987154 chr2:57987137-57987155 chr2:57987142-57987150
43	CTCF	chr2:57987740-57987890	GM12865	blood:	n/a	n/a
44	CTCF	chr2:57987100-57987250	HVMF	connective:	n/a	chr2:57987139-57987160 chr2:57987138-57987154 chr2:57987137-57987155 chr2:57987142-57987150
45	CTCF	chr2:57987060-57987210	K562	blood:	n/a	chr2:57987139-57987160 chr2:57987138-57987154 chr2:57987137-57987155 chr2:57987142-57987150
46	CTCF	chr2:57987080-57987230	HPF	lung:	n/a	chr2:57987139-57987160 chr2:57987138-57987154 chr2:57987137-57987155 chr2:57987142-57987150
47	CTCF	chr2:57987781-57987884	GM12878	blood:	n/a	n/a
48	CTCF	chr2:57987060-57987210	GM12867	blood:	n/a	chr2:57987139-57987160 chr2:57987138-57987154 chr2:57987137-57987155 chr2:57987142-57987150
49	CTCF	chr2:57986886-57987282	HCT-116	colon:	n/a	chr2:57987139-57987160 chr2:57987138-57987154 chr2:57987137-57987155 chr2:57987142-57987150
50	CTCF	chr2:57986720-57986870	AG04449	skin:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:58029565-58029615	RPTEC	kidney:	n/a
2	chr2:57986550-57986600	AG10803	skin:	n/a
3	chr2:58023996-58024046	GM12891	blood:	n/a
4	chr2:58023996-58024046	BE2_C	brain:	n/a
5	chr2:57987263-57987313	MCF-7	breast:	n/a
6	chr2:58029503-58029553	SK-N-SH	brain:	n/a
7	chr2:58023996-58024046	HUVEC	blood vessel:	n/a
8	chr2:58023996-58024046	IMR90	lung:	fetal
9	chr2:58029503-58029553	Hepatocyte	liver:	n/a
10	chr2:58029503-58029553	MCF-7	breast:	n/a
11	chr2:58029565-58029615	GM12878	blood:	n/a
12	chr2:58029503-58029553	ovcar-3	ovarian:	n/a
13	chr2:58029503-58029553	MCF10A-Er-Src	breast:	n/a
14	chr2:57987263-57987313	ProgFib	skin:	n/a
15	chr2:57987263-57987313	PANC-1	pancreas:	n/a
16	chr2:57987263-57987313	BJ	skin:	n/a
17	chr2:58029503-58029553	CMK	blood:	n/a
18	chr2:58029565-58029615	IMR90	lung:	fetal
19	chr2:58029503-58029553	AG09309	skin:	n/a
20	chr2:58023996-58024046	HAEpiC	amniotic membrane:	n/a
21	chr2:58029565-58029615	MCF10A-Er-Src	breast:	n/a
22	chr2:57986550-57986600	T-47D	breast:	n/a
23	chr2:58029565-58029615	PFSK-1	brain:	n/a
24	chr2:58023996-58024046	GM06990	blood:	n/a
25	chr2:58023996-58024046	A549	lung:	n/a
26	chr2:58023996-58024046	HRE	kidney:	n/a
27	chr2:58029565-58029615	NB4	blood:	n/a
28	chr2:58029565-58029615	U87	brain:	n/a
29	chr2:57986550-57986600	NB4	blood:	n/a
30	chr2:58029565-58029615	A549	lung:	n/a
31	chr2:57986550-57986600	HAEpiC	amniotic membrane:	n/a
32	chr2:57987263-57987313	A549	lung:	n/a
33	chr2:57987263-57987313	BE2_C	brain:	n/a
34	chr2:57987263-57987313	GM06990	blood:	n/a
35	chr2:58023996-58024046	HCPEpiC	choroid plexus:	n/a
36	chr2:58023996-58024046	SKMC	muscle:	n/a
37	chr2:58029565-58029615	HCPEpiC	choroid plexus:	n/a
38	chr2:58029503-58029553	AoSMC	blood vessel:	n/a
39	chr2:57987263-57987313	HCT-116	colon:	n/a
40	chr2:57987263-57987313	SK-N-MC	brain:	n/a
41	chr2:57987263-57987313	HAEpiC	amniotic membrane:	n/a
42	chr2:58029503-58029553	HRPEpiC	eye:	n/a
43	chr2:58023996-58024046	NHBE	bronchial:	n/a
44	chr2:58029503-58029553	SKMC	muscle:	n/a
45	chr2:58023996-58024046	BJ	skin:	n/a
46	chr2:58029503-58029553	GM19239	blood:	n/a
47	chr2:58029503-58029553	AG04450	lung:	fetal
48	chr2:57986550-57986600	NHDF-neo	bronchial:	n/a
49	chr2:58029503-58029553	NB4	blood:	n/a
50	chr2:58029503-58029553	HCT-116	colon:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:57988189..57989874-chr2:57990120..57992632,2	K562	blood:
2	chr2:58025264..58027443-chr2:58030430..58032051,2	MCF-7	breast:
3	chr2:57986735..57987942-chr2:58674900..58675939,5	MCF-7	breast:
4	chr2:58067853..58070668-chr20:48552901..48554981,2	MCF-7	breast:
5	chr2:57986668..57987445-chr2:58674884..58675821,3	K562	blood:
6	chr2:57986795..57987623-chr2:58674835..58675860,4	MCF-7	breast:
7	chr2:58003897..58005970-chr2:58009303..58012151,2	K562	blood:
8	chr2:58025264..58027443-chr2:58030430..58032051,2	MCF-7	breast:
9	chr2:58035263..58037581-chr2:58040221..58042453,2	K562	blood:
10	chr2:57947756..57948609-chr2:57986675..57987249,2	MCF-7	breast:
11	chr2:58035263..58037581-chr2:58040221..58042453,2	K562	blood:
12	chr2:58003897..58005970-chr2:58009303..58012151,2	K562	blood:
13	chr2:57988184..57990505-chr2:57993308..57996155,2	K562	blood:
14	chr2:57988184..57990505-chr2:57993308..57996155,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-VRK2-10	chr2:57982563-57982922	NONHSAT070842
2	lnc-VRK2-10	chr2:57991847-57992345	NONHSAT070842

No data

Variant related genes	Relation type
ENSG00000271615	TF binding region
ENSG00000271615	CpG island
ENSG00000271615	chromatin interactions
ENSG00000124226	chromatin interactions

Extended variants
information (count: 2186 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:2186 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1460255	chr2:57978858-57978859	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs537551165	chr2:57978875-57978876	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs557850970	chr2:57978879-57978880	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs571284572	chr2:57978926-57978927	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs188310599	chr2:57978962-57978963	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs553736142	chr2:57978963-57978964	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs114128780	chr2:57979040-57979041	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs541328302	chr2:57979064-57979065	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs536093261	chr2:57979102-57979103	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs555686348	chr2:57979108-57979109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs181169112	chr2:57979112-57979113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs544317518	chr2:57979127-57979128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs564216852	chr2:57979128-57979129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs143374512	chr2:57979184-57979185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs147137301	chr2:57979190-57979191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs34035400	chr2:57979248-57979249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs374625726	chr2:57979249-57979250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs565827554	chr2:57979275-57979276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs139486523	chr2:57979293-57979294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs149689199	chr2:57979294-57979295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs562028266	chr2:57979315-57979316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs145522565	chr2:57979320-57979321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs370588354	chr2:57979333-57979334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs79454476	chr2:57979350-57979351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs569003539	chr2:57979369-57979370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs537525483	chr2:57979392-57979393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs540098310	chr2:57979399-57979400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs369010468	chr2:57979435-57979436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs150720889	chr2:57979493-57979494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs570373206	chr2:57979496-57979497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs557463626	chr2:57979504-57979505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs537432492	chr2:57979506-57979507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs372878043	chr2:57979515-57979516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs577332590	chr2:57979561-57979562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs574425372	chr2:57979627-57979628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs535194597	chr2:57979635-57979636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs553513670	chr2:57979637-57979638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs148553529	chr2:57979659-57979660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs186436081	chr2:57979694-57979695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs144403308	chr2:57979706-57979707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs532066199	chr2:57979719-57979720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs576322503	chr2:57979761-57979762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs530264886	chr2:57979775-57979776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs562135901	chr2:57979824-57979825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs529372978	chr2:57979885-57979886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs547921734	chr2:57979909-57979910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs545894019	chr2:57979956-57979957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs146624255	chr2:57979992-57979993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs377251956	chr2:57979999-57980000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs552043846	chr2:57980081-57980082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

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
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:370 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:57979000-57983400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr2:57981000-57981200	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr2:57981200-57981400	Enhancers	Thymus	Thymus
4	chr2:57981200-57985600	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr2:57981400-57982400	Weak transcription	Thymus	Thymus
6	chr2:57981600-57982800	Enhancers	Fetal Thymus	thymus
7	chr2:57982000-57982600	Enhancers	Primary B cells from cord blood	blood
8	chr2:57982400-57982800	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr2:57982400-57982800	Enhancers	Primary B cells from peripheral blood	blood
10	chr2:57982400-57983000	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr2:57982400-57983200	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr2:57982400-57983400	Enhancers	Thymus	Thymus
13	chr2:57982600-57982800	Enhancers	H1 Cell Line	embryonic stem cell
14	chr2:57982600-57982800	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr2:57982600-57983600	Enhancers	GM12878-XiMat	blood
16	chr2:57982600-57987000	Weak transcription	Primary B cells from cord blood	blood
17	chr2:57982800-57985600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr2:57982800-57986200	Weak transcription	Primary B cells from peripheral blood	blood
19	chr2:57982800-57986200	Weak transcription	Fetal Thymus	thymus
20	chr2:57983000-57986000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr2:57983200-57985200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
22	chr2:57983400-57983600	Enhancers	Cortex derived primary cultured neurospheres	brain
23	chr2:57983400-57983800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr2:57983400-57985000	Weak transcription	HUES6 Cell Line	embryonic stem cell
25	chr2:57983400-57986000	Weak transcription	Thymus	Thymus
26	chr2:57983600-57983800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr2:57983600-57985200	Weak transcription	GM12878-XiMat	blood
28	chr2:57983600-57987200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr2:57983800-57985000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr2:57983800-57986800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr2:57985000-57985400	Weak transcription	H1 Cell Line	embryonic stem cell
32	chr2:57985000-57986800	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr2:57985000-57987200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr2:57985200-57985400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr2:57985200-57986600	Enhancers	GM12878-XiMat	blood
36	chr2:57985200-57986800	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr2:57985400-57986400	Enhancers	Brain Germinal Matrix	brain
38	chr2:57985400-57986600	Enhancers	H9 Cell Line	embryonic stem cell
39	chr2:57985400-57987400	Enhancers	H1 Cell Line	embryonic stem cell
40	chr2:57985400-57988400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr2:57985600-57985800	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr2:57985600-57986400	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr2:57985600-57987400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr2:57985800-57986200	Weak transcription	HUES64 Cell Line	embryonic stem cell
45	chr2:57985800-57986200	Enhancers	Colon Smooth Muscle	Colon
46	chr2:57985800-57986800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr2:57985800-57986800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr2:57986000-57986200	Enhancers	Brain Inferior Temporal Lobe	brain
49	chr2:57986000-57986400	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr2:57986000-57986400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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