Variant report

Variant	nsv1005681
Chromosome Location	chr2:188480281-188632003
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:560)
CpG islands
(count:184)
Chromatin interactive
region (count:34)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:560 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:188513230-188513415	K562	blood:	n/a	n/a
2	ATF1	chr2:188558759-188558891	K562	blood:	n/a	n/a
3	ATF1	chr2:188551050-188551187	K562	blood:	n/a	n/a
4	BHLHE40	chr2:188521903-188522037	K562	blood:	n/a	n/a
5	CBX3	chr2:188505670-188506206	K562	blood:	n/a	n/a
6	CCNT2	chr2:188505985-188506183	K562	blood:	n/a	n/a
7	CEBPB	chr2:188481903-188482085	K562	blood:	n/a	n/a
8	CEBPB	chr2:188608570-188608763	IMR90	lung:	n/a	chr2:188608676-188608687
9	CEBPB	chr2:188581048-188581245	A549	lung:	n/a	n/a
10	CEBPB	chr2:188553978-188554022	A549	lung:	n/a	n/a
11	CEBPB	chr2:188608563-188608828	HepG2	liver:	n/a	chr2:188608676-188608687
12	CEBPB	chr2:188626594-188626733	A549	lung:	n/a	n/a
13	CEBPB	chr2:188481819-188482019	IMR90	lung:	n/a	n/a
14	CEBPB	chr2:188481870-188482145	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr2:188481857-188482003	A549	lung:	n/a	n/a
16	CEBPB	chr2:188608641-188608753	K562	blood:	n/a	chr2:188608676-188608687
17	CTCF	chr2:188480160-188480310	HMF	breast:	n/a	n/a
18	CTCF	chr2:188480200-188480350	AG04449	skin:	n/a	n/a
19	CTCF	chr2:188523740-188523890	HMF	breast:	n/a	n/a
20	CTCF	chr2:188523740-188523890	RPTEC	kidney:	n/a	n/a
21	CTCF	chr2:188523740-188523890	HPAF	blood vessel:	n/a	n/a
22	CTCF	chr2:188499380-188499530	HPAF	blood vessel:	n/a	n/a
23	CTCF	chr2:188523720-188523870	SK-N-SH_RA	brain:	n/a	n/a
24	CTCF	chr2:188523720-188523870	AG09319	gingival:	n/a	n/a
25	CTCF	chr2:188523740-188523890	HRPEpiC	eye:	n/a	n/a
26	CTCF	chr2:188480240-188480390	AG04449	skin:	n/a	n/a
27	CTCF	chr2:188523680-188523830	HRPEpiC	eye:	n/a	n/a
28	CTCF	chr2:188523703-188524040	Gliobla	brain:	n/a	n/a
29	CTCF	chr2:188523760-188523910	GM12873	blood:	n/a	n/a
30	CTCF	chr2:188523660-188523810	HFF	foreskin:	n/a	n/a
31	CTCF	chr2:188523720-188523870	GM12869	blood:	n/a	n/a
32	CTCF	chr2:188523760-188523910	HAc	cerebellar:	n/a	n/a
33	CTCF	chr2:188524033-188524050	MCF-7	breast:	n/a	n/a
34	CTCF	chr2:188537214-188537286	Lung_OC	lung:	n/a	n/a
35	CTCF	chr2:188523780-188523930	HA-sp	spinal cord:	n/a	n/a
36	CTCF	chr2:188523740-188523904	HepG2	liver:	n/a	n/a
37	CTCF	chr2:188523810-188523822	GM19238	blood:	n/a	n/a
38	CTCF	chr2:188618175-188618211	GM20000	blood:	n/a	n/a
39	CTCF	chr2:188523740-188523890	AG09309	skin:	n/a	n/a
40	CTCF	chr2:188523740-188523890	HPF	lung:	n/a	n/a
41	CTCF	chr2:188523727-188523911	A549	lung:	n/a	n/a
42	CTCF	chr2:188523720-188523870	GM12865	blood:	n/a	n/a
43	CTCF	chr2:188523740-188523890	AG10803	skin:	n/a	n/a
44	CTCF	chr2:188536064-188536145	GM20000	blood:	n/a	n/a
45	CTCF	chr2:188523760-188523910	HFF-Myc	foreskin:	n/a	n/a
46	CTCF	chr2:188523800-188523950	GM12868	blood:	n/a	n/a
47	CTCF	chr2:188523760-188523910	GM12875	blood:	n/a	n/a
48	CTCF	chr2:188523720-188523870	GM06990	blood:	n/a	n/a
49	CTCF	chr2:188523780-188523930	WI-38	lung:	n/a	n/a
50	CTCF	chr2:188523800-188523950	GM06990	blood:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:188583082-188583132	K562	blood:	n/a
2	chr2:188583082-188583132	K562	blood:	n/a
3	chr2:188583082-188583132	A549	lung:	n/a
4	chr2:188583082-188583132	HepG2	liver:	n/a
5	chr2:188481707-188481757	PANC-1	pancreas:	n/a
6	chr2:188481707-188481757	Caco-2	colon:	n/a
7	chr2:188583082-188583132	HCF	heart:	n/a
8	chr2:188481707-188481757	GM12891	blood:	n/a
9	chr2:188583082-188583132	HNPCEpiC	eye:	n/a
10	chr2:188583082-188583132	MCF10A-Er-Src	breast:	n/a
11	chr2:188583082-188583132	BE2_C	brain:	n/a
12	chr2:188481707-188481757	SAEC	small airway:	n/a
13	chr2:188483530-188483580	CMK	blood:	n/a
14	chr2:188483530-188483580	Caco-2	colon:	n/a
15	chr2:188481707-188481757	HEEpiC	esophagus:	n/a
16	chr2:188483530-188483580	SKMC	muscle:	n/a
17	chr2:188481707-188481757	RPTEC	kidney:	n/a
18	chr2:188481707-188481757	AG09309	skin:	n/a
19	chr2:188483530-188483580	HCF	heart:	n/a
20	chr2:188583082-188583132	MCF-7	breast:	n/a
21	chr2:188483530-188483580	HAEpiC	amniotic membrane:	n/a
22	chr2:188583082-188583132	AG04450	lung:	fetal
23	chr2:188583082-188583132	NHBE	bronchial:	n/a
24	chr2:188583082-188583132	HEK293	kidney:	embryo
25	chr2:188583082-188583132	RPTEC	kidney:	n/a
26	chr2:188583082-188583132	CMK	blood:	n/a
27	chr2:188483530-188483580	HMEC	breast:	n/a
28	chr2:188483530-188483580	Hela-S3	cervix:	n/a
29	chr2:188583082-188583132	AG09309	skin:	n/a
30	chr2:188481707-188481757	IMR90	lung:	fetal
31	chr2:188583082-188583132	HRCEpiC	kidney:	n/a
32	chr2:188583082-188583132	H1-hESC	embryonic stem cell:	embryo
33	chr2:188483530-188483580	T-47D	breast:	n/a
34	chr2:188583082-188583132	HRE	kidney:	n/a
35	chr2:188483530-188483580	BJ	skin:	n/a
36	chr2:188481707-188481757	ovcar-3	ovarian:	n/a
37	chr2:188583082-188583132	IMR90	lung:	fetal
38	chr2:188583082-188583132	Jurkat	blood:	n/a
39	chr2:188483530-188483580	NH-A	brain:	n/a
40	chr2:188481707-188481757	HCPEpiC	choroid plexus:	n/a
41	chr2:188583082-188583132	GM12891	blood:	n/a
42	chr2:188583082-188583132	ECC-1	luminal epithelium:	n/a
43	chr2:188583082-188583132	Hepatocyte	liver:	n/a
44	chr2:188583082-188583132	T-47D	breast:	n/a
45	chr2:188483530-188483580	GM12878	blood:	n/a
46	chr2:188583082-188583132	NT2-D1	testis:	n/a
47	chr2:188583082-188583132	SAEC	small airway:	n/a
48	chr2:188483530-188483580	AG04449	skin:	fetal
49	chr2:188483530-188483580	AG09309	skin:	n/a
50	chr2:188583082-188583132	HRPEpiC	eye:	n/a

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:188544173..188545945-chr2:188547538..188549082,2	K562	blood:
2	chr2:188630653..188632661-chr2:188633986..188636856,2	K562	blood:
3	chr2:188480221..188482587-chr2:188496790..188498507,2	K562	blood:
4	chr2:188473583..188475657-chr2:188480041..188481763,2	K562	blood:
5	chr2:188523368..188524314-chr2:188579524..188580267,2	K562	blood:
6	chr2:188302851..188305687-chr2:188602438..188604231,2	K562	blood:
7	chr2:188480199..188482146-chr2:188486058..188487606,2	K562	blood:
8	chr2:188601766..188603906-chr2:188606320..188608826,2	K562	blood:
9	chr2:188506973..188509886-chr2:188511524..188513522,2	MCF-7	breast:
10	chr2:188478254..188481614-chr2:188483978..188486883,3	K562	blood:
11	chr2:188478443..188481336-chr2:188482033..188484662,2	K562	blood:
12	chr2:188549053..188550995-chr2:188552944..188555111,2	K562	blood:
13	chr2:188560452..188562867-chr2:188563141..188566315,4	K562	blood:
14	chr2:188506449..188508323-chr2:188511407..188513734,2	K562	blood:
15	chr2:188544173..188545945-chr2:188547538..188549082,2	K562	blood:
16	chr2:188591288..188593045-chr2:188603697..188606410,2	K562	blood:
17	chr2:188554226..188556067-chr2:188557220..188559283,2	K562	blood:
18	chr2:188523465..188524329-chr2:188707490..188708173,2	MCF-7	breast:
19	chr2:188480221..188482587-chr2:188496790..188498507,2	K562	blood:
20	chr2:188480199..188482146-chr2:188486058..188487606,2	K562	blood:
21	chr2:188478254..188481614-chr2:188483978..188486883,3	K562	blood:
22	chr2:188549053..188550995-chr2:188552944..188555111,2	K562	blood:
23	chr2:188581473..188583744-chr2:188592833..188595412,2	MCF-7	breast:
24	chr2:188478443..188481336-chr2:188482033..188484662,2	K562	blood:
25	chr2:188591288..188593045-chr2:188603697..188606410,2	K562	blood:
26	chr2:188604449..188606812-chr2:188608184..188609837,2	K562	blood:
27	chr2:188560452..188562867-chr2:188563141..188566315,4	K562	blood:
28	chr2:188506449..188508323-chr2:188511407..188513734,2	K562	blood:
29	chr2:188523368..188524314-chr2:188579524..188580267,2	K562	blood:
30	chr2:188581473..188583744-chr2:188592833..188595412,2	MCF-7	breast:
31	chr2:188601026..188603906-chr2:188607326..188609061,2	K562	blood:
32	chr2:188604449..188606812-chr2:188608184..188609837,2	K562	blood:
33	chr2:188506973..188509886-chr2:188511524..188513522,2	MCF-7	breast:
34	chr2:188554226..188556067-chr2:188557220..188559283,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DIRC1-2	chr2:188577543-188577606	ENSG00000231689

No data

Variant related genes	Relation type
ENSG00000252004	TF binding region
ENSG00000252004	CpG island
ENSG00000252004	chromatin interactions

Extended variants
information (count: 4476 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:4476 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73980910	chr2:188480289-188480290	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs185713561	chr2:188480301-188480302	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs150330621	chr2:188480306-188480307	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs547780291	chr2:188480316-188480317	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs111773915	chr2:188480322-188480323	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs137882468	chr2:188480375-188480376	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs535064204	chr2:188480413-188480414	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs577691601	chr2:188480432-188480433	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs182432282	chr2:188480436-188480437	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs71434603	chr2:188480447-188480448	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs571717127	chr2:188480448-188480449	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs188705586	chr2:188480471-188480472	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs551952417	chr2:188480474-188480475	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs10171607	chr2:188480532-188480533	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs576292404	chr2:188480557-188480558	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs368753655	chr2:188480565-188480566	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs34860546	chr2:188480590-188480591	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs201424004	chr2:188480599-188480600	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs543688028	chr2:188480630-188480631	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs565474094	chr2:188480658-188480659	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs537625892	chr2:188480689-188480690	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs547882226	chr2:188480696-188480697	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs535726374	chr2:188480714-188480715	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs371263327	chr2:188480741-188480742	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs10192794	chr2:188480803-188480804	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs192408852	chr2:188480807-188480808	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs67214938	chr2:188480853-188480854	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs374883082	chr2:188480856-188480857	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs567601765	chr2:188480938-188480939	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs538116885	chr2:188481127-188481128	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs7581500	chr2:188481130-188481131	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs140843928	chr2:188481161-188481162	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs183950944	chr2:188481177-188481178	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs553833711	chr2:188481189-188481190	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs571776506	chr2:188481198-188481199	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs111719611	chr2:188481340-188481341	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs113317635	chr2:188481357-188481358	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs557459495	chr2:188481366-188481367	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs144610052	chr2:188481382-188481383	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs7608077	chr2:188481416-188481417	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs544086690	chr2:188481482-188481483	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs558947126	chr2:188481558-188481559	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs577374698	chr2:188481559-188481560	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs541240564	chr2:188481593-188481594	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs559901745	chr2:188481596-188481597	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs539941884	chr2:188481606-188481607	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs530203710	chr2:188481623-188481624	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs188503541	chr2:188481642-188481643	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs375081181	chr2:188481669-188481670	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs113852480	chr2:188481670-188481671	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:51)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	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
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Sudden cardiac death	19188705	CNVD
Autism	19329560	CNVD
Urothelial carcinoma	21177765	CNVD
Intellectual disability	22102821	CNVD
Tetralogy of Fallot	22912587	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:502 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:188479200-188482800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr2:188479400-188480400	Enhancers	HSMM	muscle
3	chr2:188479400-188480600	Enhancers	HSMMtube	muscle
4	chr2:188479400-188484200	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr2:188479400-188485200	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr2:188479400-188485400	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr2:188479600-188480400	Enhancers	Skeletal Muscle Female	skeletal muscle
8	chr2:188479800-188480600	Enhancers	Fetal Kidney	kidney
9	chr2:188479800-188483600	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr2:188480000-188480400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr2:188480000-188480400	Enhancers	Ovary	ovary
12	chr2:188480000-188480800	Enhancers	H9 Cell Line	embryonic stem cell
13	chr2:188480000-188480800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr2:188480000-188481000	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr2:188480000-188482600	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr2:188480200-188481000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr2:188480200-188481200	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr2:188480200-188483400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr2:188480200-188484200	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr2:188480400-188480600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
21	chr2:188480400-188482000	Weak transcription	Skeletal Muscle Female	skeletal muscle
22	chr2:188480400-188482200	Weak transcription	HSMM	muscle
23	chr2:188480400-188482600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr2:188480400-188483200	Weak transcription	Ovary	ovary
25	chr2:188480400-188484400	Enhancers	Brain Germinal Matrix	brain
26	chr2:188480600-188482600	Weak transcription	HSMMtube	muscle
27	chr2:188480600-188483800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
28	chr2:188480800-188481000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr2:188480800-188481800	Weak transcription	H9 Cell Line	embryonic stem cell
30	chr2:188480800-188482200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr2:188481000-188482000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr2:188481000-188482200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
33	chr2:188481000-188482800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr2:188481200-188481600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
35	chr2:188481600-188484600	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr2:188481800-188483000	Enhancers	H9 Cell Line	embryonic stem cell
37	chr2:188481800-188483200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr2:188482000-188483000	Enhancers	H1 Cell Line	embryonic stem cell
39	chr2:188482000-188483000	Enhancers	Brain Cingulate Gyrus	brain
40	chr2:188482000-188483000	Enhancers	Skeletal Muscle Female	skeletal muscle
41	chr2:188482000-188483400	Enhancers	Brain Angular Gyrus	brain
42	chr2:188482000-188483400	Enhancers	Brain Inferior Temporal Lobe	brain
43	chr2:188482000-188483400	Enhancers	Fetal Muscle Leg	muscle
44	chr2:188482000-188483800	Enhancers	Brain Hippocampus Middle	brain
45	chr2:188482000-188484000	Enhancers	Cortex derived primary cultured neurospheres	brain
46	chr2:188482000-188484200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr2:188482200-188482600	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr2:188482200-188482800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr2:188482200-188483000	Enhancers	Brain Substantia Nigra	brain
50	chr2:188482200-188484000	Enhancers	HSMM	muscle

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