Variant report

Variant	nsv874011
Chromosome Location	chr2:49358655-49489333
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:436)
CpG islands
(count:306)
Chromatin interactive
region (count:13)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:436 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:49467819-49468047	HepG2	liver:	n/a	n/a
2	BACH1	chr2:49478947-49479134	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr2:49367907-49368045	K562	blood:	n/a	n/a
4	BATF	chr2:49456700-49457056	GM12878	blood:	n/a	n/a
5	BATF	chr2:49368436-49368647	GM12878	blood:	n/a	chr2:49368533-49368544
6	BATF	chr2:49456588-49457058	GM12878	blood:	n/a	n/a
7	BCL11A	chr2:49456598-49457072	GM12878	blood:	n/a	n/a
8	BCL11A	chr2:49456707-49457049	GM12878	blood:	n/a	n/a
9	BCL3	chr2:49475653-49475916	GM12878	blood:	n/a	n/a
10	BHLHE40	chr2:49456686-49457070	HepG2	liver:	n/a	n/a
11	BHLHE40	chr2:49437340-49437444	HepG2	liver:	n/a	n/a
12	CEBPB	chr2:49475560-49476060	A549	lung:	n/a	n/a
13	CEBPB	chr2:49389153-49389221	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr2:49475457-49476102	IMR90	lung:	n/a	n/a
15	CEBPB	chr2:49381388-49381670	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr2:49426968-49427294	HepG2	liver:	n/a	chr2:49427145-49427158 chr2:49427145-49427156 chr2:49427146-49427157
17	CEBPB	chr2:49475654-49475976	A549	lung:	n/a	n/a
18	CEBPB	chr2:49468706-49469063	IMR90	lung:	n/a	chr2:49468909-49468922 chr2:49468909-49468920
19	CEBPB	chr2:49475606-49475954	A549	lung:	n/a	n/a
20	CEBPB	chr2:49426971-49427266	A549	lung:	n/a	chr2:49427145-49427158 chr2:49427145-49427156 chr2:49427146-49427157
21	CEBPB	chr2:49478933-49479311	IMR90	lung:	n/a	n/a
22	CEBPB	chr2:49475649-49476007	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr2:49475637-49475993	HepG2	liver:	n/a	n/a
24	CEBPB	chr2:49468748-49469036	HepG2	liver:	n/a	chr2:49468909-49468922 chr2:49468909-49468920
25	CEBPB	chr2:49484910-49485040	HepG2	liver:	n/a	chr2:49484942-49484953
26	CEBPB	chr2:49468771-49469019	A549	lung:	n/a	chr2:49468909-49468922 chr2:49468909-49468920
27	CEBPD	chr2:49456704-49457038	K562	blood:	n/a	n/a
28	CTCF	chr2:49482680-49482830	HPF	lung:	n/a	n/a
29	CTCF	chr2:49442913-49443060	Kidney_OC	kidney:	n/a	n/a
30	CTCF	chr2:49436459-49436533	MCF-7	breast:	n/a	n/a
31	CTCF	chr2:49449467-49449731	IMR90	lung:	n/a	n/a
32	CTCF	chr2:49449420-49449570	AG04450	lung:	n/a	n/a
33	CTCF	chr2:49449500-49449650	HCFaa	heart:	n/a	n/a
34	CTCF	chr2:49397515-49397635	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr2:49482540-49482690	HCPEpiC	choroid plexus:	n/a	chr2:49482619-49482640
36	CTCF	chr2:49482660-49482810	NHDF-neo	bronchial:	n/a	n/a
37	CTCF	chr2:49482533-49482687	Lung_OC	lung:	n/a	chr2:49482619-49482640
38	CTCF	chr2:49437440-49437590	HepG2	liver:	n/a	n/a
39	CTCF	chr2:49482500-49482650	HMEC	breast:	n/a	chr2:49482619-49482640
40	CTCF	chr2:49482600-49482750	BE2_C	brain:	n/a	chr2:49482619-49482640
41	CTCF	chr2:49397530-49397607	GM19239	blood:	n/a	n/a
42	CTCF	chr2:49482700-49482850	A549	lung:	n/a	n/a
43	CTCF	chr2:49366260-49366410	Caco-2	colon:	n/a	n/a
44	CTCF	chr2:49482560-49482710	HMF	breast:	n/a	chr2:49482619-49482640
45	CTCF	chr2:49437480-49437630	Caco-2	colon:	n/a	n/a
46	CTCF	chr2:49482540-49482690	AG04450	lung:	n/a	chr2:49482619-49482640
47	CTCF	chr2:49482600-49482750	HRPEpiC	eye:	n/a	chr2:49482619-49482640
48	CTCF	chr2:49449548-49449642	MCF-7	breast:	n/a	n/a
49	CTCF	chr2:49397520-49397670	WERI-Rb-1	eye:	n/a	n/a
50	CTCF	chr2:49482560-49482710	HCPEpiC	choroid plexus:	n/a	chr2:49482619-49482640

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:49382401-49382451	GM12891	blood:	n/a
2	chr2:49382401-49382451	GM12891	blood:	n/a
3	chr2:49382265-49382315	K562	blood:	n/a
4	chr2:49382401-49382451	HAEpiC	amniotic membrane:	n/a
5	chr2:49382159-49382209	NT2-D1	testis:	n/a
6	chr2:49382159-49382209	BE2_C	brain:	n/a
7	chr2:49382265-49382315	GM19239	blood:	n/a
8	chr2:49381495-49381545	AG10803	skin:	n/a
9	chr2:49381495-49381545	SAEC	small airway:	n/a
10	chr2:49381495-49381545	NT2-D1	testis:	n/a
11	chr2:49380959-49381009	GM12878	blood:	n/a
12	chr2:49381495-49381545	HCF	heart:	n/a
13	chr2:49380959-49381009	Caco-2	colon:	n/a
14	chr2:49381495-49381545	A549	lung:	n/a
15	chr2:49380959-49381009	U87	brain:	n/a
16	chr2:49381495-49381545	MCF10A-Er-Src	breast:	n/a
17	chr2:49380959-49381009	IMR90	lung:	fetal
18	chr2:49382159-49382209	NHDF-neo	bronchial:	n/a
19	chr2:49380959-49381009	PANC-1	pancreas:	n/a
20	chr2:49380959-49381009	AG09319	gingival:	n/a
21	chr2:49381495-49381545	HEK293	kidney:	embryo
22	chr2:49382265-49382315	HPAEpiC	pulmonary alveolar:	n/a
23	chr2:49382265-49382315	SK-N-MC	brain:	n/a
24	chr2:49380959-49381009	AG10803	skin:	n/a
25	chr2:49380959-49381009	HL-60	blood:	n/a
26	chr2:49382159-49382209	HCF	heart:	n/a
27	chr2:49380959-49381009	HAEpiC	amniotic membrane:	n/a
28	chr2:49382265-49382315	NH-A	brain:	n/a
29	chr2:49380959-49381009	PFSK-1	brain:	n/a
30	chr2:49382159-49382209	HRCEpiC	kidney:	n/a
31	chr2:49382401-49382451	CMK	blood:	n/a
32	chr2:49382159-49382209	T-47D	breast:	n/a
33	chr2:49382401-49382451	PFSK-1	brain:	n/a
34	chr2:49382159-49382209	HCPEpiC	choroid plexus:	n/a
35	chr2:49382265-49382315	CMK	blood:	n/a
36	chr2:49382265-49382315	BE2_C	brain:	n/a
37	chr2:49382159-49382209	PANC-1	pancreas:	n/a
38	chr2:49380959-49381009	NHBE	bronchial:	n/a
39	chr2:49382265-49382315	IMR90	lung:	fetal
40	chr2:49382401-49382451	HNPCEpiC	eye:	n/a
41	chr2:49382159-49382209	U87	brain:	n/a
42	chr2:49382401-49382451	SK-N-SH_RA	brain:	n/a
43	chr2:49382401-49382451	SAEC	small airway:	n/a
44	chr2:49382159-49382209	AG10803	skin:	n/a
45	chr2:49380959-49381009	ProgFib	skin:	n/a
46	chr2:49382159-49382209	SAEC	small airway:	n/a
47	chr2:49382265-49382315	H1-hESC	embryonic stem cell:	embryo
48	chr2:49381495-49381545	PrEC	prostate:	n/a
49	chr2:49382265-49382315	Hela-S3	cervix:	n/a
50	chr2:49382265-49382315	AoSMC	blood vessel:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:49482602..49483344-chr2:49717972..49718732,2	MCF-7	breast:
2	chr2:49476946..49478961-chr2:49480994..49483698,2	K562	blood:
3	chr2:49425509..49426338-chr3:115937869..115938784,2	MCF-7	breast:
4	chr2:49467020..49468811-chr2:49494310..49496052,2	MCF-7	breast:
5	chr2:49394074..49396341-chr2:49397153..49398810,2	K562	blood:
6	chr2:49482564..49483069-chr2:50629187..50629937,2	MCF-7	breast:
7	chr2:49371083..49372770-chr2:49374962..49377778,2	K562	blood:
8	chr2:49371083..49372770-chr2:49374962..49377778,2	K562	blood:
9	chr2:49464339..49466660-chr2:49467162..49469670,2	MCF-7	breast:
10	chr2:49482441..49483071-chr2:49559200..49560186,2	MCF-7	breast:
11	chr2:49464339..49466660-chr2:49467162..49469670,2	MCF-7	breast:
12	chr2:49394074..49396341-chr2:49397153..49398810,2	K562	blood:
13	chr2:49476946..49478961-chr2:49480994..49483698,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STON1-GTF2A1L-3	chr2:49436966-49437234	NONHSAT070638
2	lnc-STON1-GTF2A1L-3	chr2:49452602-49452611	NONHSAT070638
3	lnc-STON1-GTF2A1L-3	chr2:49456719-49457043	NONHSAT070638
4	lnc-STON1-GTF2A1L-3	chr2:49437434-49437440	NONHSAT070638

No data

Variant related genes	Relation type
FSHR	TF binding region
RNU6-439P	TF binding region
FSHR	CpG island
RNU6-439P	CpG island

Extended variants
information (count: 3785 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:3785 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138606159	chr2:49373206-49373207	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs564690593	chr2:49373227-49373228	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs141709690	chr2:49373238-49373239	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs540733383	chr2:49373356-49373357	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs368706032	chr2:49373382-49373383	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs188648572	chr2:49373384-49373385	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs12473794	chr2:49373385-49373386	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs565621340	chr2:49373395-49373396	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs541851941	chr2:49373806-49373807	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs116332503	chr2:49373829-49373830	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs531249901	chr2:49373839-49373840	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs187255109	chr2:49373853-49373854	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs564779669	chr2:49373898-49373899	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs528714895	chr2:49373937-49373938	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs1504182	chr2:49373939-49373940	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs191974070	chr2:49373957-49373958	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs55655312	chr2:49374034-49374035	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs1504183	chr2:49374051-49374052	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs182645362	chr2:49374136-49374137	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs568876891	chr2:49374152-49374153	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs17038354	chr2:49374153-49374154	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs558603299	chr2:49374167-49374168	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs577049385	chr2:49374184-49374185	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs571010191	chr2:49374195-49374196	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs144227275	chr2:49374196-49374197	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs553087835	chr2:49374206-49374207	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs574596058	chr2:49374214-49374215	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs567285231	chr2:49374232-49374233	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs186794444	chr2:49374250-49374251	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs116590553	chr2:49374259-49374260	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs575340089	chr2:49374297-49374298	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs545799718	chr2:49374312-49374313	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs564667971	chr2:49374389-49374390	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs191663523	chr2:49374401-49374402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs534872903	chr2:49374421-49374422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs546880041	chr2:49374454-49374455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs562267108	chr2:49374468-49374469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs529361881	chr2:49374481-49374482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs550630499	chr2:49374489-49374490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs568986022	chr2:49374521-49374522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs369494728	chr2:49374536-49374537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs182655823	chr2:49374609-49374610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs551740127	chr2:49374616-49374617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs550020464	chr2:49374644-49374645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs534878701	chr2:49374656-49374657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs552910977	chr2:49374673-49374674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs187075933	chr2:49374685-49374686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs191972637	chr2:49374801-49374802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs557128239	chr2:49374821-49374822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs142324472	chr2:49374838-49374839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
Bladder cancer	21909424	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
small cell lung cancer	20016488	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
Lung cancer	17297452	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	20433910	CNVD
Autism	21701786	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Austim spectrum disorder	21302340	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	20553308	CNVD
Autism	22241247	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Retinoblastoma	22278416	CNVD
Cancer	21183584	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	18768390	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	18940311	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18945720	CNVD
Schizophrenia	19571808	CNVD
Prostate cancer	16573809	CNVD
Neuroticism	17667963	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19546859	CNVD
Autism	17322880	CNVD
Lung cancer	17086460	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Hereditary non-polyposis colorectal cancer	19566914	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:261 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:49373200-49373400	Enhancers	HSMMtube	muscle
2	chr2:49373800-49374400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr2:49373800-49376400	Weak transcription	HSMMtube	muscle
4	chr2:49374400-49376400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr2:49376400-49376600	Enhancers	HSMMtube	muscle
6	chr2:49376400-49377200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr2:49376400-49377400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr2:49376400-49377800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr2:49376600-49379800	Weak transcription	HSMMtube	muscle
10	chr2:49377200-49379600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr2:49377400-49380400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr2:49377800-49379400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr2:49379400-49381800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr2:49379600-49380200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr2:49379800-49380000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr2:49379800-49381200	Flanking Active TSS	HSMMtube	muscle
17	chr2:49380000-49380400	Flanking Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr2:49380000-49380400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr2:49380000-49380800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr2:49380000-49381200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr2:49380000-49381200	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr2:49380000-49381400	Active TSS	Ovary	ovary
23	chr2:49380000-49382200	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr2:49380000-49382200	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr2:49380000-49382400	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr2:49380000-49382600	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr2:49380200-49380400	Enhancers	H9 Cell Line	embryonic stem cell
28	chr2:49380200-49380400	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr2:49380200-49380600	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr2:49380200-49380600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr2:49380200-49381200	Enhancers	Fetal Heart	heart
32	chr2:49380200-49382400	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr2:49380400-49381000	Active TSS	Fetal Muscle Leg	muscle
34	chr2:49380400-49381200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr2:49380400-49381400	Weak transcription	H9 Cell Line	embryonic stem cell
36	chr2:49380400-49381400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr2:49380400-49382400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr2:49380600-49381800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
39	chr2:49380600-49382200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr2:49381000-49381200	Weak transcription	Fetal Muscle Leg	muscle
41	chr2:49381200-49381400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr2:49381200-49381400	Enhancers	HSMMtube	muscle
43	chr2:49381200-49381600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
44	chr2:49381200-49381600	Flanking Active TSS	Fetal Heart	heart
45	chr2:49381200-49381600	Enhancers	Fetal Muscle Leg	muscle
46	chr2:49381200-49381600	Active TSS	Right Atrium	heart
47	chr2:49381200-49382000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr2:49381400-49381600	Flanking Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr2:49381400-49381600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr2:49381400-49381600	Enhancers	Left Ventricle	heart

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