Variant report

Variant	nsv874081
Chromosome Location	chr2:51975932-52062108
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:391)
CpG islands
(count:244)
Chromatin interactive
region (count:21)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:391 , 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	ARID3A	chr2:51985283-51985521	HepG2	liver:	n/a	n/a
2	BACH1	chr2:52013621-52013717	H1-hESC	embryonic stem cell:	n/a	n/a
3	CBX3	chr2:52040441-52040852	HCT-116	colon:	n/a	n/a
4	CEBPB	chr2:52040288-52040929	HCT-116	colon:	n/a	n/a
5	CEBPB	chr2:51991789-51992037	IMR90	lung:	n/a	chr2:51991926-51991937
6	CEBPB	chr2:52051683-52051729	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr2:52020223-52020461	HepG2	liver:	n/a	chr2:52020327-52020338 chr2:52020277-52020288
8	CEBPB	chr2:52010516-52010845	A549	lung:	n/a	chr2:52010684-52010695
9	CEBPB	chr2:51991600-51992080	Hela-S3	cervix:	n/a	chr2:51991926-51991937
10	CEBPB	chr2:52052956-52053358	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr2:52020231-52020456	A549	lung:	n/a	chr2:52020327-52020338 chr2:52020277-52020288
12	CEBPB	chr2:52057394-52057709	IMR90	lung:	n/a	n/a
13	CEBPB	chr2:51991752-51992063	HepG2	liver:	n/a	chr2:51991926-51991937
14	CEBPB	chr2:52017155-52017401	IMR90	lung:	n/a	n/a
15	CEBPB	chr2:52010523-52010856	IMR90	lung:	n/a	chr2:52010684-52010695
16	CEBPB	chr2:52040458-52040757	IMR90	lung:	n/a	n/a
17	CEBPB	chr2:52020207-52020467	IMR90	lung:	n/a	chr2:52020327-52020338 chr2:52020277-52020288
18	CEBPB	chr2:52010535-52010824	HepG2	liver:	n/a	chr2:52010684-52010695
19	CEBPB	chr2:52040436-52040772	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr2:52057437-52057715	HepG2	liver:	n/a	n/a
21	CEBPB	chr2:52051511-52051735	A549	lung:	n/a	n/a
22	CTCF	chr2:52022760-52022910	MCF-7	breast:	n/a	n/a
23	CTCF	chr2:52022760-52022910	HEEpiC	esophagus:	n/a	n/a
24	CTCF	chr2:52022752-52022962	GM12878	blood:	n/a	n/a
25	CTCF	chr2:52022640-52022790	A549	lung:	n/a	n/a
26	CTCF	chr2:52022780-52022930	GM12873	blood:	n/a	n/a
27	CTCF	chr2:52022860-52023010	HMEC	breast:	n/a	n/a
28	CTCF	chr2:52022720-52022870	HFF-Myc	foreskin:	n/a	n/a
29	CTCF	chr2:52022720-52022870	HMF	breast:	n/a	n/a
30	CTCF	chr2:52022740-52022890	HMF	breast:	n/a	n/a
31	CTCF	chr2:52022800-52022950	MCF-7	breast:	n/a	n/a
32	CTCF	chr2:52022760-52022910	A549	lung:	n/a	n/a
33	CTCF	chr2:52022759-52022897	LNCaP	prostate:	n/a	n/a
34	CTCF	chr2:52022760-52022910	HPF	lung:	n/a	n/a
35	CTCF	chr2:52022860-52023010	GM12867	blood:	n/a	n/a
36	CTCF	chr2:52022607-52023034	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr2:52022740-52022890	GM12873	blood:	n/a	n/a
38	CTCF	chr2:52022637-52022911	HepG2	liver:	n/a	n/a
39	CTCF	chr2:52022760-52022910	HCM	heart:	n/a	n/a
40	CTCF	chr2:52022780-52022930	NB4	blood:	n/a	n/a
41	CTCF	chr2:52022760-52022910	HPAF	blood vessel:	n/a	n/a
42	CTCF	chr2:52022780-52022930	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr2:52022760-52022910	GM12874	blood:	n/a	n/a
44	CTCF	chr2:52022740-52022890	SAEC	small airway:	n/a	n/a
45	CTCF	chr2:52022719-52022957	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr2:52022760-52022910	RPTEC	kidney:	n/a	n/a
47	CTCF	chr2:52022720-52022870	GM12870	blood:	n/a	n/a
48	CTCF	chr2:52022778-52022888	NHEK	skin:	n/a	n/a
49	CTCF	chr2:52022700-52022850	AG04449	skin:	n/a	n/a
50	CTCF	chr2:52022880-52023030	WI-38	lung:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:52006728-52006778	IMR90	lung:	fetal
2	chr2:52006728-52006778	AoSMC	blood vessel:	n/a
3	chr2:52039654-52039704	GM06990	blood:	n/a
4	chr2:52007665-52007715	NHBE	bronchial:	n/a
5	chr2:52007582-52007632	SK-N-SH	brain:	n/a
6	chr2:52007665-52007715	K562	blood:	n/a
7	chr2:52007665-52007715	NH-A	brain:	n/a
8	chr2:52006728-52006778	Hela-S3	cervix:	n/a
9	chr2:52006728-52006778	K562	blood:	n/a
10	chr2:52039654-52039704	GM12878	blood:	n/a
11	chr2:52039654-52039704	HPAEpiC	pulmonary alveolar:	n/a
12	chr2:52007665-52007715	AG09309	skin:	n/a
13	chr2:52006728-52006778	LNCaP	prostate:	n/a
14	chr2:52007582-52007632	BJ	skin:	n/a
15	chr2:52007582-52007632	GM12878	blood:	n/a
16	chr2:52039654-52039704	NB4	blood:	n/a
17	chr2:52007582-52007632	ovcar-3	ovarian:	n/a
18	chr2:52007582-52007632	Jurkat	blood:	n/a
19	chr2:52007665-52007715	HL-60	blood:	n/a
20	chr2:52007665-52007715	A549	lung:	n/a
21	chr2:52007665-52007715	HIPEpiC	eye:	n/a
22	chr2:52007665-52007715	BJ	skin:	n/a
23	chr2:52007582-52007632	BE2_C	brain:	n/a
24	chr2:52039654-52039704	H1-hESC	embryonic stem cell:	embryo
25	chr2:52007665-52007715	ProgFib	skin:	n/a
26	chr2:52006728-52006778	MCF10A-Er-Src	breast:	n/a
27	chr2:52006728-52006778	Hepatocyte	liver:	n/a
28	chr2:52039654-52039704	HL-60	blood:	n/a
29	chr2:52039654-52039704	Hela-S3	cervix:	n/a
30	chr2:52006728-52006778	HEEpiC	esophagus:	n/a
31	chr2:52039654-52039704	Hepatocyte	liver:	n/a
32	chr2:52039654-52039704	T-47D	breast:	n/a
33	chr2:52039654-52039704	HCPEpiC	choroid plexus:	n/a
34	chr2:52007582-52007632	HPAEpiC	pulmonary alveolar:	n/a
35	chr2:52006728-52006778	RPTEC	kidney:	n/a
36	chr2:52039654-52039704	HepG2	liver:	n/a
37	chr2:52006728-52006778	SAEC	small airway:	n/a
38	chr2:52039654-52039704	ovcar-3	ovarian:	n/a
39	chr2:52007582-52007632	HIPEpiC	eye:	n/a
40	chr2:52039654-52039704	BE2_C	brain:	n/a
41	chr2:52007665-52007715	HRPEpiC	eye:	n/a
42	chr2:52039654-52039704	Jurkat	blood:	n/a
43	chr2:52007582-52007632	PFSK-1	brain:	n/a
44	chr2:52007665-52007715	HNPCEpiC	eye:	n/a
45	chr2:52007665-52007715	Caco-2	colon:	n/a
46	chr2:52039654-52039704	SK-N-MC	brain:	n/a
47	chr2:52007665-52007715	HCT-116	colon:	n/a
48	chr2:52007582-52007632	T-47D	breast:	n/a
49	chr2:52039654-52039704	U87	brain:	n/a
50	chr2:52039654-52039704	K562	blood:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	2:51664217-51674289..2:51974300-51979334	H1-hESC	embryonic stem cell:	embryo
2	chr2:52013693..52015857-chr2:52040010..52042547,2	K562	blood:
3	chr2:51969395..51971476-chr2:51980845..51983747,2	K562	blood:
4	2:51664217-51674289..2:52034460-52043624	GM12878	blood:
5	2:52043909-52049825..2:52049825-52050373	K562	blood:
6	2:51664217-51674289..2:51983874-51990011	GM12878	blood:
7	2:51681598-51686731..2:51983874-51990011	GM12878	blood:
8	chr2:52045177..52047183-chr2:52049220..52051220,2	K562	blood:
9	2:51664217-51674289..2:52006946-52008886	H1-hESC	embryonic stem cell:	embryo
10	chr2:50756714..50757394-chr2:52022672..52023233,2	MCF-7	breast:
11	chr2:52045177..52047313-chr2:52049220..52051486,2	K562	blood:
12	chr2:52002782..52005199-chr2:52008928..52011159,2	K562	blood:
13	2:51745267-51754233..2:52043624-52043909	K562	blood:
14	2:51664217-51674289..2:52055539-52058793	H1-hESC	embryonic stem cell:	embryo
15	chr2:52045177..52047313-chr2:52049220..52051486,2	K562	blood:
16	chr2:52045177..52047183-chr2:52049220..52051220,2	K562	blood:
17	chr2:52002782..52005199-chr2:52008928..52011159,2	K562	blood:
18	chr2:52013693..52015857-chr2:52040010..52042547,2	K562	blood:
19	2:51664217-51674289..2:52043909-52049825	H1-hESC	embryonic stem cell:	embryo
20	2:52043909-52049825..2:52049825-52050373	K562	blood:
21	2:51755125-51764739..2:52034460-52043624	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHAC2-4	chr2:51989227-51989312	ENSG00000231918.1

No data

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

Extended variants
information (count: 1953 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:1953 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545768508	chr2:51984404-51984405	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs535959787	chr2:51984408-51984409	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs141737116	chr2:51984451-51984452	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs78102925	chr2:51984458-51984459	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs17863691	chr2:51984459-51984460	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs546535638	chr2:51984495-51984496	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs11563113	chr2:51984518-51984519	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs192278733	chr2:51984519-51984520	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs148054710	chr2:51984535-51984536	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs112562050	chr2:51984571-51984572	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs568913638	chr2:51984591-51984592	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs534424218	chr2:51984643-51984644	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs557779430	chr2:51984659-51984660	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs566522158	chr2:51984741-51984742	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs182886674	chr2:51984755-51984756	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs554206483	chr2:51984785-51984786	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs17868236	chr2:51984788-51984789	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs28965172	chr2:51984809-51984810	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs34287517	chr2:51984834-51984835	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs548533916	chr2:51984845-51984846	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs73930761	chr2:51984873-51984874	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs372260423	chr2:51984884-51984885	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs76592305	chr2:51984889-51984890	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs567261938	chr2:51984975-51984976	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs193116928	chr2:51985022-51985023	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs537495787	chr2:51985179-51985180	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs564135399	chr2:51985182-51985183	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs371481932	chr2:51985199-51985200	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs557850120	chr2:51985212-51985213	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs11418028	chr2:51985213-51985214	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs528422394	chr2:51985218-51985219	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs150619089	chr2:51985230-51985231	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs367546093	chr2:51985237-51985238	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs76082681	chr2:51985241-51985242	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs371860228	chr2:51985258-51985259	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs563275550	chr2:51985263-51985264	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs568999382	chr2:51985269-51985270	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs576715906	chr2:51985275-51985276	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs11563265	chr2:51985286-51985287	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs551451352	chr2:51985306-51985307	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs139676629	chr2:51985316-51985317	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs533732309	chr2:51985344-51985345	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs369143465	chr2:51985378-51985379	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs187699129	chr2:51985392-51985393	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs116770505	chr2:51985422-51985423	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs535805741	chr2:51985423-51985424	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs144723401	chr2:51985446-51985447	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs575478552	chr2:51985448-51985449	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs559490617	chr2:51985454-51985455	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs11563085	chr2:51985455-51985456	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:84)

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
Bipolar disorder	19114987	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:83 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:51984400-51985800	Enhancers	Hela-S3	cervix
2	chr2:51986600-51987200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr2:51987200-51987800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr2:51987800-51988000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr2:51999600-52001800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr2:52001800-52002200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
7	chr2:52005600-52007000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr2:52005600-52007000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr2:52005800-52006800	ZNF genes & repeats	HepG2	liver
10	chr2:52006000-52006400	Enhancers	Fetal Muscle Leg	muscle
11	chr2:52006000-52006400	Active TSS	Osteobl	bone
12	chr2:52006800-52008000	Weak transcription	HepG2	liver
13	chr2:52006800-52011000	Weak transcription	Right Atrium	heart
14	chr2:52007000-52009400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr2:52008000-52008400	ZNF genes & repeats	HepG2	liver
16	chr2:52008800-52009400	Enhancers	Fetal Brain Male	brain
17	chr2:52009000-52012000	Enhancers	Fetal Heart	heart
18	chr2:52009400-52009800	Weak transcription	Fetal Brain Male	brain
19	chr2:52009400-52009800	Enhancers	Pancreatic Islets	Pancreatic Islet
20	chr2:52009400-52010800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr2:52009800-52010200	Weak transcription	Pancreatic Islets	Pancreatic Islet
22	chr2:52009800-52011400	Enhancers	Fetal Brain Male	brain
23	chr2:52010000-52010400	Enhancers	Fetal Brain Female	brain
24	chr2:52010000-52010600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr2:52010000-52010600	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr2:52010000-52010600	Enhancers	HMEC	breast
27	chr2:52010200-52010600	Enhancers	NHDF-Ad	bronchial
28	chr2:52010200-52010800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr2:52010200-52010800	Enhancers	Skeletal Muscle Female	skeletal muscle
30	chr2:52010200-52011000	Enhancers	Pancreatic Islets	Pancreatic Islet
31	chr2:52011000-52011600	Weak transcription	Pancreatic Islets	Pancreatic Islet
32	chr2:52011600-52011800	Enhancers	Pancreatic Islets	Pancreatic Islet
33	chr2:52016800-52018000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr2:52017000-52017400	Enhancers	Osteobl	bone
35	chr2:52017000-52017600	Enhancers	Adipose Nuclei	Adipose
36	chr2:52018000-52019000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr2:52019000-52019200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr2:52022000-52022400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr2:52022000-52022600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr2:52022000-52022800	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr2:52022200-52022600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr2:52022400-52022800	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr2:52022400-52023000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr2:52032400-52032800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
45	chr2:52032400-52032800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
46	chr2:52032800-52035200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr2:52035200-52035400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
48	chr2:52037200-52037600	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr2:52037600-52038400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
50	chr2:52038200-52039200	Enhancers	Hela-S3	cervix

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links