Variant report

Variant	nsv998637
Chromosome Location	chr2:52370482-52527949
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:331)
CpG islands
(count:61)
Chromatin interactive
region (count:7)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:331 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:52467445-52467547	K562	blood:	n/a	n/a
2	BRCA1	chr2:52412674-52412755	GM12878	blood:	n/a	n/a
3	CEBPB	chr2:52488046-52488388	IMR90	lung:	n/a	n/a
4	CEBPB	chr2:52496591-52497101	IMR90	lung:	n/a	chr2:52496760-52496771
5	CEBPB	chr2:52508166-52508428	IMR90	lung:	n/a	chr2:52508316-52508327
6	CEBPB	chr2:52437849-52438049	IMR90	lung:	n/a	n/a
7	CEBPB	chr2:52424571-52424862	HepG2	liver:	n/a	chr2:52424680-52424691
8	CEBPB	chr2:52497321-52497563	HepG2	liver:	n/a	chr2:52497433-52497444
9	CEBPB	chr2:52493705-52493946	IMR90	lung:	n/a	n/a
10	CEBPB	chr2:52424578-52424825	A549	lung:	n/a	chr2:52424680-52424691
11	CEBPB	chr2:52475213-52475267	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr2:52484597-52484933	IMR90	lung:	n/a	chr2:52484762-52484773 chr2:52484763-52484772 chr2:52484761-52484774 chr2:52484761-52484772
13	CEBPB	chr2:52484592-52484943	HepG2	liver:	n/a	chr2:52484762-52484773 chr2:52484763-52484772 chr2:52484761-52484774 chr2:52484761-52484772
14	CEBPB	chr2:52475176-52475438	HepG2	liver:	n/a	chr2:52475269-52475280
15	CEBPB	chr2:52516375-52516634	IMR90	lung:	n/a	chr2:52516470-52516481
16	CEBPB	chr2:52496622-52496897	A549	lung:	n/a	chr2:52496760-52496771
17	CEBPB	chr2:52434940-52435407	HepG2	liver:	n/a	n/a
18	CEBPB	chr2:52447446-52447926	ECC-1	luminal epithelium:	n/a	n/a
19	CEBPB	chr2:52484634-52484917	A549	lung:	n/a	chr2:52484762-52484773 chr2:52484763-52484772 chr2:52484761-52484774 chr2:52484761-52484772
20	CEBPB	chr2:52508157-52508457	HepG2	liver:	n/a	chr2:52508316-52508327
21	CEBPB	chr2:52516890-52517212	IMR90	lung:	n/a	n/a
22	CEBPB	chr2:52475235-52475401	A549	lung:	n/a	chr2:52475269-52475280
23	CEBPB	chr2:52516417-52516634	HepG2	liver:	n/a	chr2:52516470-52516481
24	CEBPB	chr2:52424527-52424851	IMR90	lung:	n/a	chr2:52424680-52424691
25	CEBPB	chr2:52516875-52517234	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr2:52424565-52424782	Hela-S3	cervix:	n/a	chr2:52424680-52424691
27	CEBPB	chr2:52496637-52496874	HepG2	liver:	n/a	chr2:52496760-52496771
28	CEBPB	chr2:52447440-52447956	ECC-1	luminal epithelium:	n/a	n/a
29	CHD2	chr2:52480885-52480914	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr2:52456925-52457018	NHEK	skin:	n/a	n/a
31	CTCF	chr2:52474540-52474690	HCT-116	colon:	n/a	n/a
32	CTCF	chr2:52491800-52491950	HCPEpiC	choroid plexus:	n/a	n/a
33	CTCF	chr2:52371840-52371990	Hela-S3	cervix:	n/a	n/a
34	CTCF	chr2:52524865-52524936	Lung_OC	lung:	n/a	n/a
35	CTCF	chr2:52371799-52372551	IMR90	lung:	n/a	chr2:52372370-52372391
36	CTCF	chr2:52371918-52372041	Gliobla	brain:	n/a	n/a
37	CTCF	chr2:52371880-52372030	AoAF	blood vessel:	n/a	n/a
38	CTCF	chr2:52372270-52372490	GM12878	blood:	n/a	chr2:52372370-52372391
39	CTCF	chr2:52371880-52372030	HMF	breast:	n/a	n/a
40	CTCF	chr2:52371840-52371990	HCT-116	colon:	n/a	n/a
41	CTCF	chr2:52456920-52457018	GM12892	blood:	n/a	n/a
42	CTCF	chr2:52371920-52372070	HCPEpiC	choroid plexus:	n/a	n/a
43	CTCF	chr2:52456919-52457017	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr2:52408003-52408026	GM13976	blood:	n/a	n/a
45	CTCF	chr2:52456945-52456997	MCF-7	breast:	n/a	n/a
46	CTCF	chr2:52497009-52497059	A549	lung:	n/a	n/a
47	CTCF	chr2:52456921-52457008	GM19238	blood:	n/a	n/a
48	CTCF	chr2:52372320-52372470	HCPEpiC	choroid plexus:	n/a	chr2:52372370-52372391
49	CTCF	chr2:52371820-52371970	HPAF	blood vessel:	n/a	n/a
50	CTCF	chr2:52371900-52372050	HA-sp	spinal cord:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:52480467-52480517	HCPEpiC	choroid plexus:	n/a
2	chr2:52480467-52480517	HUVEC	blood vessel:	n/a
3	chr2:52480467-52480517	HNPCEpiC	eye:	n/a
4	chr2:52480467-52480517	Hepatocyte	liver:	n/a
5	chr2:52480467-52480517	NH-A	brain:	n/a
6	chr2:52480467-52480517	ECC-1	luminal epithelium:	n/a
7	chr2:52480467-52480517	SKMC	muscle:	n/a
8	chr2:52480467-52480517	PFSK-1	brain:	n/a
9	chr2:52480467-52480517	RPTEC	kidney:	n/a
10	chr2:52480467-52480517	Hela-S3	cervix:	n/a
11	chr2:52480467-52480517	HCM	heart:	n/a
12	chr2:52480467-52480517	GM06990	blood:	n/a
13	chr2:52480467-52480517	NB4	blood:	n/a
14	chr2:52480467-52480517	U87	brain:	n/a
15	chr2:52480467-52480517	BJ	skin:	n/a
16	chr2:52480467-52480517	HIPEpiC	eye:	n/a
17	chr2:52480467-52480517	MCF-7	breast:	n/a
18	chr2:52480467-52480517	SAEC	small airway:	n/a
19	chr2:52480467-52480517	LNCaP	prostate:	n/a
20	chr2:52480467-52480517	HRPEpiC	eye:	n/a
21	chr2:52480467-52480517	IMR90	lung:	fetal
22	chr2:52480467-52480517	SK-N-MC	brain:	n/a
23	chr2:52480467-52480517	HepG2	liver:	n/a
24	chr2:52480467-52480517	A549	lung:	n/a
25	chr2:52480467-52480517	NHDF-neo	bronchial:	n/a
26	chr2:52480467-52480517	Jurkat	blood:	n/a
27	chr2:52480467-52480517	ovcar-3	ovarian:	n/a
28	chr2:52480467-52480517	T-47D	breast:	n/a
29	chr2:52480467-52480517	HCT-116	colon:	n/a
30	chr2:52480467-52480517	Caco-2	colon:	n/a
31	chr2:52480467-52480517	HAEpiC	amniotic membrane:	n/a
32	chr2:52480467-52480517	AG04449	skin:	fetal
33	chr2:52480467-52480517	SK-N-SH	brain:	n/a
34	chr2:52480467-52480517	K562	blood:	n/a
35	chr2:52480467-52480517	SK-N-SH_RA	brain:	n/a
36	chr2:52480467-52480517	HPAEpiC	pulmonary alveolar:	n/a
37	chr2:52480467-52480517	NT2-D1	testis:	n/a
38	chr2:52480467-52480517	HRCEpiC	kidney:	n/a
39	chr2:52480467-52480517	AG04450	lung:	fetal
40	chr2:52480467-52480517	HEK293	kidney:	embryo
41	chr2:52480467-52480517	PrEC	prostate:	n/a
42	chr2:52480467-52480517	H1-hESC	embryonic stem cell:	embryo
43	chr2:52480467-52480517	HRE	kidney:	n/a
44	chr2:52480467-52480517	PANC-1	pancreas:	n/a
45	chr2:52480467-52480517	GM12878	blood:	n/a
46	chr2:52480467-52480517	AG09319	gingival:	n/a
47	chr2:52480467-52480517	GM12892	blood:	n/a
48	chr2:52480467-52480517	GM19239	blood:	n/a
49	chr2:52480467-52480517	HMEC	breast:	n/a
50	chr2:52480467-52480517	CMK	blood:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:52521422..52524399-chr2:52528510..52532522,3	K562	blood:
2	chr2:52476747..52479271-chr2:52487226..52489997,2	K562	blood:
3	chr2:52476747..52479271-chr2:52487226..52489997,2	K562	blood:
4	chr2:52444137..52446093-chr2:52447228..52448981,2	K562	blood:
5	chr2:52444137..52446093-chr2:52447228..52448981,2	K562	blood:
6	chr2:52367783..52370728-chr2:52370744..52372935,2	K562	blood:
7	chr2:52367783..52370728-chr2:52370744..52372935,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHAC2-10	chr2:52453760-52453813	NONHSAT070667
2	lnc-CHAC2-10	chr2:52470105-52470654	NONHSAT070667

No data

Variant related genes	Relation type
ENSG00000202195	TF binding region
ENSG00000202195	CpG island

Extended variants
information (count: 2698 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:2698 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192950583	chr2:52370518-52370519	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs11886202	chr2:52370572-52370573	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs7564560	chr2:52370579-52370580	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs76763193	chr2:52370587-52370588	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs111329432	chr2:52370588-52370589	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs375277925	chr2:52370622-52370623	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs183597377	chr2:52370655-52370656	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs528439188	chr2:52370733-52370734	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs542220449	chr2:52370745-52370746	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs561802529	chr2:52370748-52370749	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs374985732	chr2:52370805-52370806	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs186819856	chr2:52370887-52370888	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs574196821	chr2:52370903-52370904	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs533051098	chr2:52370926-52370927	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs570697422	chr2:52370934-52370935	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs533603579	chr2:52370946-52370947	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs542985132	chr2:52371003-52371004	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs562959996	chr2:52371006-52371007	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs146319442	chr2:52371021-52371022	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs534275206	chr2:52371055-52371056	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs191579074	chr2:52371085-52371086	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs184833720	chr2:52371091-52371092	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs537126464	chr2:52371104-52371105	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs190780169	chr2:52371135-52371136	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs576461251	chr2:52371138-52371139	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs576932244	chr2:52371162-52371163	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs371952183	chr2:52371167-52371168	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs375318019	chr2:52371220-52371221	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs545991711	chr2:52371228-52371229	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs79865844	chr2:52371253-52371254	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs370780273	chr2:52371254-52371255	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs138415247	chr2:52371267-52371268	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs541807828	chr2:52371297-52371298	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs561739278	chr2:52371310-52371311	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs7594573	chr2:52371363-52371364	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs142926583	chr2:52371399-52371400	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs116137274	chr2:52371420-52371421	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs533330639	chr2:52371433-52371434	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs528277950	chr2:52371450-52371451	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs548088296	chr2:52371459-52371460	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs562138236	chr2:52371479-52371480	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs77372193	chr2:52371495-52371496	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs531044567	chr2:52371500-52371501	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs201318482	chr2:52371519-52371520	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs77569656	chr2:52371524-52371525	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs199917277	chr2:52371527-52371528	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs371918920	chr2:52371528-52371529	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs116442495	chr2:52371537-52371538	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs181529339	chr2:52371538-52371539	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs13029158	chr2:52371543-52371544	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:85)

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
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
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
Schizophrenia	23813976	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:153 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:52368400-52372000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr2:52370400-52371800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr2:52370400-52372400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr2:52370400-52372400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr2:52372000-52372400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr2:52373000-52373400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr2:52385200-52385800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr2:52385800-52389800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr2:52389200-52389600	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr2:52389200-52389600	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr2:52389800-52390000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr2:52408000-52408400	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr2:52408000-52408400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr2:52412800-52413000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr2:52419200-52419400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr2:52419200-52421200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr2:52419200-52421200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr2:52419400-52420400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr2:52420400-52421600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr2:52427600-52427800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr2:52434800-52435000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr2:52435000-52435200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr2:52435200-52435400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr2:52435400-52435600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr2:52435600-52435800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr2:52436800-52437200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr2:52436800-52438600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr2:52437400-52438000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr2:52442000-52443800	Enhancers	Fetal Heart	heart
30	chr2:52443800-52448600	Weak transcription	Fetal Heart	heart
31	chr2:52448600-52449800	Enhancers	Fetal Heart	heart
32	chr2:52449400-52449800	Enhancers	NHDF-Ad	bronchial
33	chr2:52449600-52450000	Active TSS	Primary T helper naive cells from peripheral blood	blood
34	chr2:52451600-52452600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr2:52452600-52454600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr2:52454600-52455200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr2:52463200-52464000	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr2:52463400-52463800	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr2:52463400-52463800	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr2:52463800-52464000	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr2:52463800-52464600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr2:52463800-52466000	Weak transcription	HUES48 Cell Line	embryonic stem cell
43	chr2:52464000-52464400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr2:52464400-52465000	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr2:52464600-52464800	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr2:52464800-52465800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
47	chr2:52465000-52466200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr2:52465800-52466000	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr2:52465800-52466400	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr2:52465800-52466400	Enhancers	iPS-18 Cell Line	embryonic stem cell

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