Variant report

Variant	nsv523090
Chromosome Location	chr2:149037012-149110873
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr2:149108418-149108678	IMR90	lung:	n/a	chr2:149108533-149108546 chr2:149108534-149108545 chr2:149108533-149108546 chr2:149108533-149108544 chr2:149108533-149108546
2	CEBPB	chr2:149107861-149108193	Hela-S3	cervix:	n/a	chr2:149107998-149108011 chr2:149108084-149108095 chr2:149108000-149108011 chr2:149108084-149108097 chr2:149107998-149108011 chr2:149108084-149108097 chr2:149108084-149108095 chr2:149107998-149108011 chr2:149108000-149108011
3	CEBPB	chr2:149036791-149037095	IMR90	lung:	n/a	chr2:149036949-149036960
4	CEBPB	chr2:149038716-149038999	IMR90	lung:	n/a	chr2:149038862-149038873
5	CEBPB	chr2:149038752-149038930	A549	lung:	n/a	chr2:149038862-149038873
6	CEBPB	chr2:149038733-149038964	H1-hESC	embryonic stem cell:	n/a	chr2:149038862-149038873
7	CEBPB	chr2:149036828-149037142	HepG2	liver:	n/a	chr2:149036949-149036960
8	CEBPB	chr2:149045883-149046183	IMR90	lung:	n/a	n/a
9	CEBPB	chr2:149036788-149037114	HepG2	liver:	n/a	chr2:149036949-149036960
10	CEBPB	chr2:149057291-149057499	IMR90	lung:	n/a	n/a
11	CEBPB	chr2:149108389-149108611	A549	lung:	n/a	chr2:149108533-149108546 chr2:149108534-149108545 chr2:149108533-149108546 chr2:149108533-149108544 chr2:149108533-149108546
12	CEBPB	chr2:149108364-149108667	HepG2	liver:	n/a	chr2:149108533-149108546 chr2:149108534-149108545 chr2:149108533-149108546 chr2:149108533-149108544 chr2:149108533-149108546
13	CEBPB	chr2:149108396-149108615	Hela-S3	cervix:	n/a	chr2:149108533-149108546 chr2:149108534-149108545 chr2:149108533-149108546 chr2:149108533-149108544 chr2:149108533-149108546
14	CEBPB	chr2:149063181-149063185	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr2:149036772-149037160	MCF-7	breast:	n/a	chr2:149036949-149036960
16	CEBPB	chr2:149038725-149038955	HepG2	liver:	n/a	chr2:149038862-149038873
17	CEBPB	chr2:149036882-149037075	K562	blood:	n/a	chr2:149036949-149036960
18	CEBPB	chr2:149036906-149037097	H1-hESC	embryonic stem cell:	n/a	chr2:149036949-149036960
19	CEBPB	chr2:149036854-149037024	HepG2	liver:	n/a	chr2:149036949-149036960
20	CEBPB	chr2:149036773-149037143	HepG2	liver:	n/a	chr2:149036949-149036960
21	CTCF	chr2:149109880-149110030	HBMEC	blood vessel:	n/a	n/a
22	CTCF	chr2:149092798-149092853	GM10248	blood:	n/a	n/a
23	CTCF	chr2:149075218-149075274	GM20000	blood:	n/a	n/a
24	CTCF	chr2:149042079-149042098	ProgFib	skin:	n/a	n/a
25	CTCF	chr2:149038180-149038330	Hela-S3	cervix:	n/a	n/a
26	CTCF	chr2:149100928-149100933	GM20000	blood:	n/a	n/a
27	CTCF	chr2:149092744-149092792	GM10248	blood:	n/a	n/a
28	CTCF	chr2:149073733-149073779	LNCaP	prostate:	n/a	n/a
29	CUX1	chr2:149044355-149044363	GM12878	blood:	n/a	n/a
30	E2F4	chr2:149060619-149060819	MCF10A-Er-Src	breast:	n/a	n/a
31	E2F4	chr2:149095882-149096395	MCF10A-Er-Src	breast:	n/a	n/a
32	E2F4	chr2:149098436-149098536	MCF10A-Er-Src	breast:	n/a	n/a
33	E2F4	chr2:149043260-149043385	MCF10A-Er-Src	breast:	n/a	n/a
34	E2F4	chr2:149046023-149046216	MCF10A-Er-Src	breast:	n/a	n/a
35	EGR1	chr2:149055754-149056180	ECC-1	luminal epithelium:	n/a	n/a
36	FOS	chr2:149039727-149040203	MCF10A-Er-Src	breast:	n/a	chr2:149039991-149040002
37	FOS	chr2:149045959-149046206	MCF10A-Er-Src	breast:	n/a	chr2:149046069-149046080
38	FOS	chr2:149055852-149056108	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr2:149057123-149057482	HUVEC	blood vessel:	n/a	n/a
40	FOS	chr2:149039669-149040214	HUVEC	blood vessel:	n/a	chr2:149039991-149040002
41	FOS	chr2:149039661-149040181	MCF10A-Er-Src	breast:	n/a	chr2:149039991-149040002
42	FOS	chr2:149055836-149056109	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr2:149039692-149040182	MCF10A-Er-Src	breast:	n/a	chr2:149039991-149040002
44	FOS	chr2:149109085-149109254	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr2:149039733-149040170	MCF10A-Er-Src	breast:	n/a	chr2:149039991-149040002
46	FOS	chr2:149045982-149046221	MCF10A-Er-Src	breast:	n/a	chr2:149046069-149046080
47	FOS	chr2:149046002-149046265	MCF10A-Er-Src	breast:	n/a	chr2:149046069-149046080
48	FOS	chr2:149096093-149096450	MCF10A-Er-Src	breast:	n/a	chr2:149096274-149096284 chr2:149096273-149096284 chr2:149096274-149096284 chr2:149096307-149096315 chr2:149096275-149096283 chr2:149096305-149096316 chr2:149096274-149096284 chr2:149096274-149096284
49	FOS	chr2:149096107-149096470	MCF10A-Er-Src	breast:	n/a	chr2:149096274-149096284 chr2:149096273-149096284 chr2:149096274-149096284 chr2:149096307-149096315 chr2:149096275-149096283 chr2:149096305-149096316 chr2:149096274-149096284 chr2:149096274-149096284
50	FOS	chr2:149095725-149096655	HUVEC	blood vessel:	n/a	chr2:149096274-149096284 chr2:149096273-149096284 chr2:149096274-149096284 chr2:149096307-149096315 chr2:149096275-149096283 chr2:149096305-149096316 chr2:149096274-149096284 chr2:149096274-149096284

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:149041060-149041110	HIPEpiC	eye:	n/a
2	chr2:149096527-149096577	MCF10A-Er-Src	breast:	n/a
3	chr2:149041060-149041110	T-47D	breast:	n/a
4	chr2:149041060-149041110	A549	lung:	n/a
5	chr2:149063092-149063142	HCT-116	colon:	n/a
6	chr2:149063092-149063142	HL-60	blood:	n/a
7	chr2:149096527-149096577	SK-N-SH	brain:	n/a
8	chr2:149063092-149063142	HEEpiC	esophagus:	n/a
9	chr2:149096527-149096577	HCPEpiC	choroid plexus:	n/a
10	chr2:149063092-149063142	AG09319	gingival:	n/a
11	chr2:149041060-149041110	NHDF-neo	bronchial:	n/a
12	chr2:149041060-149041110	AG09319	gingival:	n/a
13	chr2:149063092-149063142	ProgFib	skin:	n/a
14	chr2:149096527-149096577	Jurkat	blood:	n/a
15	chr2:149096527-149096577	HMEC	breast:	n/a
16	chr2:149063092-149063142	HRE	kidney:	n/a
17	chr2:149041060-149041110	ovcar-3	ovarian:	n/a
18	chr2:149096527-149096577	GM12891	blood:	n/a
19	chr2:149096527-149096577	A549	lung:	n/a
20	chr2:149041060-149041110	HRPEpiC	eye:	n/a
21	chr2:149096527-149096577	AG09319	gingival:	n/a
22	chr2:149063092-149063142	BJ	skin:	n/a
23	chr2:149096527-149096577	HIPEpiC	eye:	n/a
24	chr2:149041060-149041110	HUVEC	blood vessel:	n/a
25	chr2:149063092-149063142	MCF-7	breast:	n/a
26	chr2:149096527-149096577	BJ	skin:	n/a
27	chr2:149063092-149063142	PrEC	prostate:	n/a
28	chr2:149041060-149041110	HAEpiC	amniotic membrane:	n/a
29	chr2:149096527-149096577	AG10803	skin:	n/a
30	chr2:149096527-149096577	LNCaP	prostate:	n/a
31	chr2:149096527-149096577	ECC-1	luminal epithelium:	n/a
32	chr2:149096527-149096577	HCM	heart:	n/a
33	chr2:149063092-149063142	GM06990	blood:	n/a
34	chr2:149041060-149041110	U87	brain:	n/a
35	chr2:149063092-149063142	HNPCEpiC	eye:	n/a
36	chr2:149063092-149063142	GM12878	blood:	n/a
37	chr2:149063092-149063142	AG04449	skin:	fetal
38	chr2:149041060-149041110	HCPEpiC	choroid plexus:	n/a
39	chr2:149063092-149063142	PFSK-1	brain:	n/a
40	chr2:149063092-149063142	SKMC	muscle:	n/a
41	chr2:149096527-149096577	K562	blood:	n/a
42	chr2:149063092-149063142	MCF10A-Er-Src	breast:	n/a
43	chr2:149063092-149063142	H1-hESC	embryonic stem cell:	embryo
44	chr2:149063092-149063142	NB4	blood:	n/a
45	chr2:149041060-149041110	RPTEC	kidney:	n/a
46	chr2:149041060-149041110	GM12891	blood:	n/a
47	chr2:149041060-149041110	MCF-7	breast:	n/a
48	chr2:149096527-149096577	PANC-1	pancreas:	n/a
49	chr2:149063092-149063142	PANC-1	pancreas:	n/a
50	chr2:149063092-149063142	HEK293	kidney:	embryo

No.	Distal block	Cell Line	Cell type
1	chr2:149098190..149099193-chr8:103870990..103871561,3	MCF-7	breast:
2	chr2:149075837..149077502-chr2:149078187..149080957,2	K562	blood:
3	chr2:149075837..149077502-chr2:149078187..149080957,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MBD5-1	chr2:149099783-149099905	NONHSAT074871
2	lnc-ORC4-3	chr2:149053225-149054248	NONHSAT074880
3	lnc-MBD5-1	chr2:149099783-149099905	NONHSAT074872
4	lnc-MBD5-1	chr2:149099783-149099905	NONHSAT074878

Variant related genes	Relation type
ENSG00000224007	TF binding region
ENSG00000224007	CpG island

Extended variants
information (count: 2702 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:2702 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7605678	chr2:149037012-149037013	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs544870881	chr2:149037053-149037054	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs187247984	chr2:149037058-149037059	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs539982877	chr2:149037126-149037127	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs558060853	chr2:149037151-149037152	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs190574440	chr2:149037199-149037200	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs563169062	chr2:149037201-149037202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs140603593	chr2:149037214-149037215	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs182453710	chr2:149037286-149037287	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs551664164	chr2:149037336-149037337	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs560761233	chr2:149037359-149037360	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs541167017	chr2:149037366-149037367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs1377455	chr2:149037442-149037443	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs118004463	chr2:149037455-149037456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs549072178	chr2:149037464-149037465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs531779202	chr2:149037465-149037466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs567105576	chr2:149037483-149037484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs530860993	chr2:149037489-149037490	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs77771832	chr2:149037527-149037528	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs76502513	chr2:149037528-149037529	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs201582913	chr2:149037571-149037572	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs556106560	chr2:149037628-149037629	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs377717508	chr2:149037638-149037639	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs372953399	chr2:149037701-149037702	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs71840405	chr2:149037711-149037712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs567292070	chr2:149037714-149037715	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs549405899	chr2:149037715-149037716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs58474751	chr2:149037719-149037720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs201241891	chr2:149037720-149037721	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs199562723	chr2:149037726-149037727	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs199684907	chr2:149037736-149037737	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs528044137	chr2:149037768-149037769	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs115581000	chr2:149037777-149037778	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs571361577	chr2:149037825-149037826	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs538353561	chr2:149037893-149037894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs529057909	chr2:149037958-149037959	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs12691782	chr2:149037994-149037995	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs192685868	chr2:149038102-149038103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs555592142	chr2:149038114-149038115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs79732421	chr2:149038150-149038151	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs541453790	chr2:149038243-149038244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs553086903	chr2:149038259-149038260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs578068959	chr2:149038285-149038286	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs145654654	chr2:149038336-149038337	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs563487801	chr2:149038345-149038346	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs1542323	chr2:149038402-149038403	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs367912604	chr2:149038472-149038473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs570418654	chr2:149038479-149038480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs528366597	chr2:149038528-149038529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs546622607	chr2:149038603-149038604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Mental retardation	22214275	CNVD
Glioblastoma	21080181	CNVD
small cell lung cancer	20016488	CNVD
Epilepsy	19904302	CNVD
Intellectual disability	19904302	CNVD
Microcephaly	19904302	CNVD
severe speech impairment	19904302	CNVD
Mental retardation	20152051	CNVD
2q23.1 microdeletion syndrome	18812405	CNVD
Mental retardation	19809484	CNVD
Autism	21981781	CNVD
Mental retardation	17847001	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Autism	20531469	CNVD

Chromatin state (count:607 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:149012600-149043400	Weak transcription	Gastric	stomach
2	chr2:149012800-149096000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr2:149017200-149038000	Weak transcription	Primary B cells from cord blood	blood
4	chr2:149017400-149037600	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr2:149017400-149050600	Weak transcription	Thymus	Thymus
6	chr2:149017400-149062800	Weak transcription	Fetal Lung	lung
7	chr2:149017400-149070600	Weak transcription	Primary hematopoietic stem cells	blood
8	chr2:149017600-149043400	Weak transcription	Fetal Stomach	stomach
9	chr2:149017600-149049000	Weak transcription	Duodenum Mucosa	Duodenum
10	chr2:149017600-149060800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
11	chr2:149023600-149039200	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr2:149025800-149044600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr2:149026000-149045000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr2:149026000-149070400	Weak transcription	Fetal Intestine Small	intestine
15	chr2:149027000-149039200	Weak transcription	Pancreatic Islets	Pancreatic Islet
16	chr2:149027600-149038000	Weak transcription	GM12878-XiMat	blood
17	chr2:149029400-149055400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr2:149030200-149039200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr2:149031000-149041400	Weak transcription	Duodenum Smooth Muscle	Duodenum
20	chr2:149031400-149039400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr2:149031400-149040400	Weak transcription	Aorta	Aorta
22	chr2:149031400-149042000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr2:149031400-149079000	Weak transcription	Left Ventricle	heart
24	chr2:149031600-149046200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr2:149031600-149055200	Weak transcription	Primary T cells from cord blood	blood
26	chr2:149036600-149037200	Enhancers	NHDF-Ad	bronchial
27	chr2:149036600-149038200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr2:149036600-149047000	Weak transcription	Primary T helper cells fromperipheralblood	blood
29	chr2:149036800-149037200	Enhancers	HepG2	liver
30	chr2:149037200-149038400	Enhancers	Dnd41	blood
31	chr2:149037200-149039400	Weak transcription	NHDF-Ad	bronchial
32	chr2:149037200-149041200	Weak transcription	HepG2	liver
33	chr2:149037400-149037600	Enhancers	Primary B cells from peripheral blood	blood
34	chr2:149038000-149038200	Enhancers	GM12878-XiMat	blood
35	chr2:149038000-149038400	Enhancers	Primary B cells from cord blood	blood
36	chr2:149038400-149044800	Weak transcription	Primary B cells from cord blood	blood
37	chr2:149038800-149039600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr2:149039200-149039400	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr2:149039200-149039400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr2:149039200-149039400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr2:149039200-149039600	Enhancers	Pancreatic Islets	Pancreatic Islet
42	chr2:149039200-149040000	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr2:149039400-149039600	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr2:149039400-149039600	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr2:149039400-149039600	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr2:149039400-149039600	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr2:149039400-149039600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
48	chr2:149039400-149040000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr2:149039400-149040200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr2:149039400-149040400	Enhancers	NHDF-Ad	bronchial

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