Variant report

Variant	nsv521318
Chromosome Location	chr2:55716650-55736704
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:163)
CpG islands
(count:61)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:163 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:55727308-55727534	K562	blood:	n/a	n/a
2	ATF3	chr2:55716695-55717073	HCT-116	colon:	n/a	n/a
3	BACH1	chr2:55727252-55727522	K562	blood:	n/a	n/a
4	BACH1	chr2:55717835-55718065	K562	blood:	n/a	chr2:55717897-55717911
5	BACH1	chr2:55717677-55718117	H1-hESC	embryonic stem cell:	n/a	chr2:55717897-55717911
6	BACH1	chr2:55727236-55727462	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr2:55727291-55727547	GM12878	blood:	n/a	n/a
8	BATF	chr2:55727303-55727514	GM12878	blood:	n/a	n/a
9	BHLHE40	chr2:55717856-55717871	K562	blood:	n/a	n/a
10	CBX3	chr2:55717657-55718073	K562	blood:	n/a	n/a
11	CBX3	chr2:55730401-55730882	K562	blood:	n/a	n/a
12	CEBPB	chr2:55727220-55727418	K562	blood:	n/a	chr2:55727360-55727371
13	CEBPB	chr2:55727119-55727565	A549	lung:	n/a	chr2:55727360-55727371
14	CEBPB	chr2:55727188-55727556	K562	blood:	n/a	chr2:55727360-55727371
15	CEBPB	chr2:55727174-55727553	Hela-S3	cervix:	n/a	chr2:55727360-55727371
16	CEBPB	chr2:55716677-55716979	HepG2	liver:	n/a	chr2:55716802-55716813
17	CEBPB	chr2:55727046-55727716	A549	lung:	n/a	chr2:55727360-55727371
18	CEBPB	chr2:55716669-55716962	A549	lung:	n/a	chr2:55716802-55716813
19	CEBPB	chr2:55727283-55727417	HepG2	liver:	n/a	chr2:55727360-55727371
20	CEBPB	chr2:55716625-55717140	HCT-116	colon:	n/a	chr2:55716802-55716813
21	CEBPB	chr2:55720513-55720635	IMR90	lung:	n/a	n/a
22	CEBPB	chr2:55727126-55727603	HCT-116	colon:	n/a	chr2:55727360-55727371
23	CEBPB	chr2:55727192-55727550	HepG2	liver:	n/a	chr2:55727360-55727371
24	CEBPB	chr2:55727152-55727560	K562	blood:	n/a	chr2:55727360-55727371
25	CEBPB	chr2:55716557-55717114	HCT-116	colon:	n/a	chr2:55716802-55716813
26	CEBPB	chr2:55727182-55727554	A549	lung:	n/a	chr2:55727360-55727371
27	CEBPB	chr2:55727148-55727724	HCT-116	colon:	n/a	chr2:55727360-55727371
28	CEBPB	chr2:55716643-55716948	H1-hESC	embryonic stem cell:	n/a	chr2:55716802-55716813
29	CEBPB	chr2:55716682-55716951	IMR90	lung:	n/a	chr2:55716802-55716813
30	CEBPB	chr2:55727170-55727574	IMR90	lung:	n/a	chr2:55727360-55727371
31	CEBPB	chr2:55716620-55716993	K562	blood:	n/a	chr2:55716802-55716813
32	CTCF	chr2:55730420-55730570	HepG2	liver:	n/a	n/a
33	CTCF	chr2:55719075-55719161	K562	blood:	n/a	chr2:55719102-55719112
34	CTCF	chr2:55732520-55732670	HepG2	liver:	n/a	n/a
35	CTCF	chr2:55730530-55730602	MCF-7	breast:	n/a	n/a
36	CTCF	chr2:55719080-55719230	HepG2	liver:	n/a	chr2:55719102-55719112
37	CTCF	chr2:55730340-55730490	MCF-7	breast:	n/a	n/a
38	CTCF	chr2:55730300-55730450	HCT-116	colon:	n/a	n/a
39	CTCF	chr2:55730060-55730210	HepG2	liver:	n/a	n/a
40	CTCF	chr2:55732500-55732650	HCT-116	colon:	n/a	n/a
41	CTCF	chr2:55730300-55730450	A549	lung:	n/a	n/a
42	CTCF	chr2:55730560-55730710	HCT-116	colon:	n/a	n/a
43	CTCF	chr2:55730360-55730510	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr2:55718954-55719221	K562	blood:	n/a	chr2:55719102-55719112
45	CUX1	chr2:55727287-55727476	K562	blood:	n/a	n/a
46	E2F4	chr2:55717707-55718081	MCF10A-Er-Src	breast:	n/a	chr2:55717893-55717900
47	E2F4	chr2:55727267-55727513	MCF10A-Er-Src	breast:	n/a	n/a
48	ELF1	chr2:55730319-55730701	K562	blood:	n/a	chr2:55730513-55730526
49	EP300	chr2:55717812-55718012	K562	blood:	n/a	chr2:55717899-55717908
50	FOS	chr2:55716617-55716999	MCF10A-Er-Src	breast:	n/a	chr2:55716694-55716706

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:55717980-55718030	HRE	kidney:	n/a
2	chr2:55717980-55718030	ovcar-3	ovarian:	n/a
3	chr2:55717980-55718030	PANC-1	pancreas:	n/a
4	chr2:55717980-55718030	SK-N-MC	brain:	n/a
5	chr2:55717980-55718030	IMR90	lung:	fetal
6	chr2:55717980-55718030	HL-60	blood:	n/a
7	chr2:55717980-55718030	Hepatocyte	liver:	n/a
8	chr2:55717980-55718030	HNPCEpiC	eye:	n/a
9	chr2:55717980-55718030	NH-A	brain:	n/a
10	chr2:55717980-55718030	AG04450	lung:	fetal
11	chr2:55717980-55718030	Hela-S3	cervix:	n/a
12	chr2:55717980-55718030	HAEpiC	amniotic membrane:	n/a
13	chr2:55717980-55718030	HPAEpiC	pulmonary alveolar:	n/a
14	chr2:55717980-55718030	GM12892	blood:	n/a
15	chr2:55717980-55718030	PrEC	prostate:	n/a
16	chr2:55717980-55718030	BE2_C	brain:	n/a
17	chr2:55717980-55718030	HRCEpiC	kidney:	n/a
18	chr2:55717980-55718030	Jurkat	blood:	n/a
19	chr2:55717980-55718030	SAEC	small airway:	n/a
20	chr2:55717980-55718030	HCT-116	colon:	n/a
21	chr2:55717980-55718030	NHBE	bronchial:	n/a
22	chr2:55717980-55718030	AG09319	gingival:	n/a
23	chr2:55717980-55718030	SKMC	muscle:	n/a
24	chr2:55717980-55718030	AoSMC	blood vessel:	n/a
25	chr2:55717980-55718030	NT2-D1	testis:	n/a
26	chr2:55717980-55718030	NHDF-neo	bronchial:	n/a
27	chr2:55717980-55718030	ECC-1	luminal epithelium:	n/a
28	chr2:55717980-55718030	HRPEpiC	eye:	n/a
29	chr2:55717980-55718030	HEEpiC	esophagus:	n/a
30	chr2:55717980-55718030	MCF10A-Er-Src	breast:	n/a
31	chr2:55717980-55718030	HCM	heart:	n/a
32	chr2:55717980-55718030	PFSK-1	brain:	n/a
33	chr2:55717980-55718030	H1-hESC	embryonic stem cell:	embryo
34	chr2:55717980-55718030	GM06990	blood:	n/a
35	chr2:55717980-55718030	SK-N-SH_RA	brain:	n/a
36	chr2:55717980-55718030	AG10803	skin:	n/a
37	chr2:55717980-55718030	MCF-7	breast:	n/a
38	chr2:55717980-55718030	RPTEC	kidney:	n/a
39	chr2:55717980-55718030	HCF	heart:	n/a
40	chr2:55717980-55718030	HEK293	kidney:	embryo
41	chr2:55717980-55718030	Caco-2	colon:	n/a
42	chr2:55717980-55718030	GM19239	blood:	n/a
43	chr2:55717980-55718030	ProgFib	skin:	n/a
44	chr2:55717980-55718030	U87	brain:	n/a
45	chr2:55717980-55718030	BJ	skin:	n/a
46	chr2:55717980-55718030	HMEC	breast:	n/a
47	chr2:55717980-55718030	K562	blood:	n/a
48	chr2:55717980-55718030	SK-N-SH	brain:	n/a
49	chr2:55717980-55718030	HCPEpiC	choroid plexus:	n/a
50	chr2:55717980-55718030	GM12891	blood:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:55734348..55736732-chr2:55747645..55749289,2	K562	blood:
2	chr2:55733547..55736199-chr2:55744050..55746817,2	MCF-7	breast:
3	chr2:55719796..55722184-chr2:55731465..55733382,2	MCF-7	breast:
4	chr2:55641621..55644231-chr2:55715263..55717892,2	K562	blood:
5	chr2:55463589..55465767-chr2:55732207..55734884,2	MCF-7	breast:
6	chr2:55735103..55738045-chr2:55741187..55743259,2	K562	blood:
7	chr2:55716556..55719523-chr2:55721485..55723403,3	K562	blood:
8	chr2:55726280..55728850-chr2:55731449..55734016,2	K562	blood:
9	chr2:55459396..55462117-chr2:55715734..55717681,2	K562	blood:
10	chr2:55716414..55718011-chr2:55844321..55846630,2	K562	blood:
11	chr2:55719796..55722184-chr2:55731465..55733382,2	MCF-7	breast:
12	chr2:55720808..55723210-chr2:55837791..55839820,2	MCF-7	breast:
13	chr2:55731157..55733900-chr2:55736800..55738554,2	MCF-7	breast:
14	chr2:55716556..55719523-chr2:55720351..55723403,5	K562	blood:
15	chr2:55716556..55719523-chr2:55720351..55723403,5	K562	blood:
16	chr2:55728050..55729964-chr2:55747020..55749706,2	MCF-7	breast:
17	chr2:55716556..55719523-chr2:55721485..55723403,3	K562	blood:
18	chr2:55709620..55711839-chr2:55714950..55717947,2	K562	blood:
19	chr2:55714333..55716529-chr2:55717522..55719586,2	K562	blood:
20	chr2:55727452..55730813-chr2:55743534..55747364,4	K562	blood:

No data

Variant related genes	Relation type
RNU6-634P	TF binding region
RNU6-634P	CpG island
ENSG00000143947	chromatin interactions
ENSG00000163001	chromatin interactions
ENSG00000138041	chromatin interactions
ENSG00000272606	chromatin interactions
ENSG00000162994	chromatin interactions
ENSG00000239189	chromatin interactions

Extended variants
information (count: 771 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:771 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17792521	chr2:55716650-55716651	Weak transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs372658523	chr2:55716662-55716663	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs532849553	chr2:55716670-55716671	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs17792539	chr2:55716683-55716684	Weak transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs545675897	chr2:55716706-55716707	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs565519687	chr2:55716708-55716709	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs151329420	chr2:55716709-55716710	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs554384093	chr2:55716798-55716799	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs17792577	chr2:55716801-55716802	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs111774616	chr2:55716802-55716803	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs141826033	chr2:55716803-55716804	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs372552424	chr2:55716828-55716829	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs576765845	chr2:55716887-55716888	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs191720807	chr2:55716922-55716923	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs558935544	chr2:55716941-55716942	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs78492285	chr2:55716943-55716944	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs74622170	chr2:55716948-55716949	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs528282783	chr2:55717057-55717058	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs548043806	chr2:55717069-55717070	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs541378510	chr2:55717079-55717080	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs78064605	chr2:55717080-55717081	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs530178937	chr2:55717093-55717094	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs182555841	chr2:55717119-55717120	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs186884854	chr2:55717149-55717150	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs192529609	chr2:55717184-55717185	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs532886903	chr2:55717260-55717261	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs552580496	chr2:55717292-55717293	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs553915737	chr2:55717297-55717298	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs540003793	chr2:55717395-55717396	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs566330469	chr2:55717403-55717404	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs572099411	chr2:55717533-55717534	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs548123429	chr2:55717535-55717536	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs72801575	chr2:55717552-55717553	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs570453060	chr2:55717612-55717613	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs539475707	chr2:55717640-55717641	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs536738000	chr2:55717648-55717649	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs550407402	chr2:55717695-55717696	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs570290677	chr2:55717702-55717703	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs147088531	chr2:55717718-55717719	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs115236656	chr2:55717740-55717741	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs373865956	chr2:55717761-55717762	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs116725201	chr2:55717823-55717824	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs541110835	chr2:55717894-55717895	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs554995547	chr2:55717898-55717899	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs575034595	chr2:55717899-55717900	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs138443474	chr2:55717958-55717959	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs563908955	chr2:55718029-55718030	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs552802996	chr2:55718056-55718057	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs577528772	chr2:55718084-55718085	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs546350789	chr2:55718088-55718089	Enhancers Weak transcription	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
Williams Syndrome	20824207	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
Ependymoma	20639864	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:80 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:55710000-55716800	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr2:55711000-55717000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr2:55715000-55717800	Weak transcription	K562	blood
4	chr2:55715600-55717400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr2:55716800-55717000	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr2:55716800-55717000	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr2:55716800-55717000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr2:55716800-55717200	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr2:55716800-55717400	Enhancers	NHEK	skin
10	chr2:55717000-55717200	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr2:55717000-55717600	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr2:55717000-55717800	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr2:55717000-55718000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr2:55717000-55718200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr2:55717000-55718400	Enhancers	Brain Substantia Nigra	brain
16	chr2:55717000-55718800	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr2:55717200-55717400	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr2:55717200-55718000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr2:55717200-55718200	Weak transcription	HUES48 Cell Line	embryonic stem cell
20	chr2:55717400-55717800	Weak transcription	NHEK	skin
21	chr2:55717400-55718000	Weak transcription	HUES64 Cell Line	embryonic stem cell
22	chr2:55717400-55718000	Enhancers	Fetal Muscle Leg	muscle
23	chr2:55717400-55718000	Enhancers	NHLF	lung
24	chr2:55717400-55718200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr2:55717400-55718400	Enhancers	Muscle Satellite Cultured Cells	--
26	chr2:55717400-55718600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr2:55717600-55718000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr2:55717600-55718000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr2:55717600-55718000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr2:55717600-55718000	Enhancers	Fetal Muscle Trunk	muscle
31	chr2:55717600-55718600	Enhancers	Brain Inferior Temporal Lobe	brain
32	chr2:55717800-55718000	Enhancers	Ovary	ovary
33	chr2:55717800-55718000	Enhancers	K562	blood
34	chr2:55717800-55718000	Enhancers	NHEK	skin
35	chr2:55717800-55718400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
36	chr2:55717800-55718400	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr2:55717800-55718400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr2:55717800-55718600	Enhancers	Cortex derived primary cultured neurospheres	brain
39	chr2:55717800-55718800	Enhancers	HSMM	muscle
40	chr2:55717800-55720000	Enhancers	Brain Germinal Matrix	brain
41	chr2:55718000-55718400	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr2:55718000-55718600	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr2:55718000-55718600	Weak transcription	K562	blood
44	chr2:55718000-55718800	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr2:55718000-55718800	Enhancers	iPS-20b Cell Line	embryonic stem cell
46	chr2:55718000-55718800	Enhancers	Brain Hippocampus Middle	brain
47	chr2:55718000-55719000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr2:55718000-55720200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr2:55718000-55720200	Weak transcription	NHEK	skin
50	chr2:55718200-55718400	Enhancers	HUVEC	blood vessel

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