Variant report

Variant	nsv1011800
Chromosome Location	chr2:188301324-188340396
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:747)
CpG islands
(count:62)
Chromatin interactive
region (count:21)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:747 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:188326188-188326206	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:188326415-188326867	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:188317827-188318187	K562	blood:	n/a	n/a
4	ATF2	chr2:188312809-188313314	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr2:188340176-188341023	GM12878	blood:	n/a	n/a
6	BATF	chr2:188340236-188340498	GM12878	blood:	n/a	chr2:188340405-188340416
7	BATF	chr2:188340301-188340499	GM12878	blood:	n/a	chr2:188340405-188340416
8	BATF	chr2:188327674-188327939	GM12878	blood:	n/a	chr2:188327699-188327707
9	BCL11A	chr2:188340195-188340620	GM12878	blood:	n/a	n/a
10	BCL11A	chr2:188340271-188340482	GM12878	blood:	n/a	n/a
11	BCLAF1	chr2:188312648-188313438	GM12878	blood:	n/a	n/a
12	BCLAF1	chr2:188312732-188313340	GM12878	blood:	n/a	n/a
13	BHLHE40	chr2:188312812-188313323	GM12878	blood:	n/a	n/a
14	BRCA1	chr2:188326379-188326862	HepG2	liver:	n/a	n/a
15	BRCA1	chr2:188313072-188313272	GM12878	blood:	n/a	n/a
16	CBX3	chr2:188312772-188313268	K562	blood:	n/a	n/a
17	CBX3	chr2:188312818-188313395	HCT-116	colon:	n/a	n/a
18	CBX3	chr2:188312808-188313187	HCT-116	colon:	n/a	n/a
19	CEBPB	chr2:188312878-188313270	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr2:188312961-188313147	K562	blood:	n/a	n/a
21	CEBPB	chr2:188307539-188307878	A549	lung:	n/a	chr2:188307585-188307596 chr2:188307583-188307596 chr2:188307703-188307712 chr2:188307701-188307712 chr2:188307702-188307713
22	CEBPB	chr2:188307537-188307886	HepG2	liver:	n/a	chr2:188307585-188307596 chr2:188307583-188307596 chr2:188307703-188307712 chr2:188307701-188307712 chr2:188307702-188307713
23	CEBPB	chr2:188314715-188314989	A549	lung:	n/a	chr2:188314843-188314854 chr2:188314745-188314757
24	CEBPB	chr2:188314779-188314995	IMR90	lung:	n/a	chr2:188314843-188314854
25	CEBPB	chr2:188325614-188325870	A549	lung:	n/a	n/a
26	CEBPB	chr2:188307541-188307882	K562	blood:	n/a	chr2:188307585-188307596 chr2:188307583-188307596 chr2:188307703-188307712 chr2:188307701-188307712 chr2:188307702-188307713
27	CEBPB	chr2:188312955-188313166	MCF-7	breast:	n/a	n/a
28	CEBPB	chr2:188307531-188307888	IMR90	lung:	n/a	chr2:188307585-188307596 chr2:188307583-188307596 chr2:188307703-188307712 chr2:188307701-188307712 chr2:188307702-188307713
29	CEBPB	chr2:188314800-188314996	HepG2	liver:	n/a	chr2:188314843-188314854
30	CEBPB	chr2:188312901-188313183	HepG2	liver:	n/a	n/a
31	CEBPB	chr2:188312869-188313236	IMR90	lung:	n/a	n/a
32	CEBPB	chr2:188314794-188314995	K562	blood:	n/a	chr2:188314843-188314854
33	CEBPB	chr2:188312856-188313215	K562	blood:	n/a	n/a
34	CEBPB	chr2:188325576-188325734	K562	blood:	n/a	n/a
35	CEBPB	chr2:188307554-188307828	H1-hESC	embryonic stem cell:	n/a	chr2:188307585-188307596 chr2:188307583-188307596 chr2:188307703-188307712 chr2:188307701-188307712 chr2:188307702-188307713
36	CEBPB	chr2:188325687-188325804	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr2:188312799-188313229	ECC-1	luminal epithelium:	n/a	n/a
38	CEBPB	chr2:188325640-188325904	HepG2	liver:	n/a	n/a
39	CEBPB	chr2:188312883-188313212	K562	blood:	n/a	n/a
40	CEBPB	chr2:188312895-188313248	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr2:188325686-188325849	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr2:188333087-188333162	HepG2	liver:	n/a	n/a
43	CEBPB	chr2:188321192-188321424	K562	blood:	n/a	n/a
44	CEBPB	chr2:188325575-188325925	IMR90	lung:	n/a	chr2:188325911-188325919
45	CEBPZ	chr2:188326562-188326754	HepG2	liver:	n/a	n/a
46	CHD1	chr2:188312848-188313460	GM12878	blood:	n/a	n/a
47	CHD2	chr2:188326799-188326901	K562	blood:	n/a	n/a
48	CHD2	chr2:188312761-188313306	GM12878	blood:	n/a	n/a
49	CHD2	chr2:188326265-188326986	HepG2	liver:	n/a	n/a
50	CREB1	chr2:188340217-188340684	GM12878	blood:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:188312833-188312883	HepG2	liver:	n/a
2	chr2:188312833-188312883	HepG2	liver:	n/a
3	chr2:188312833-188312883	K562	blood:	n/a
4	chr2:188312833-188312883	HNPCEpiC	eye:	n/a
5	chr2:188312833-188312883	HCT-116	colon:	n/a
6	chr2:188312833-188312883	AG04450	lung:	fetal
7	chr2:188312833-188312883	HCF	heart:	n/a
8	chr2:188312833-188312883	Jurkat	blood:	n/a
9	chr2:188312833-188312883	GM12891	blood:	n/a
10	chr2:188312833-188312883	HPAEpiC	pulmonary alveolar:	n/a
11	chr2:188312833-188312883	HEEpiC	esophagus:	n/a
12	chr2:188312833-188312883	SKMC	muscle:	n/a
13	chr2:188312833-188312883	BE2_C	brain:	n/a
14	chr2:188312833-188312883	ovcar-3	ovarian:	n/a
15	chr2:188312833-188312883	BJ	skin:	n/a
16	chr2:188312833-188312883	SK-N-MC	brain:	n/a
17	chr2:188312833-188312883	MCF10A-Er-Src	breast:	n/a
18	chr2:188312833-188312883	HAEpiC	amniotic membrane:	n/a
19	chr2:188312833-188312883	GM06990	blood:	n/a
20	chr2:188312833-188312883	NHBE	bronchial:	n/a
21	chr2:188312833-188312883	HEK293	kidney:	embryo
22	chr2:188312833-188312883	HUVEC	blood vessel:	n/a
23	chr2:188312833-188312883	HRPEpiC	eye:	n/a
24	chr2:188312833-188312883	H1-hESC	embryonic stem cell:	embryo
25	chr2:188312833-188312883	NH-A	brain:	n/a
26	chr2:188312833-188312883	AG04449	skin:	fetal
27	chr2:188312833-188312883	T-47D	breast:	n/a
28	chr2:188312833-188312883	AG09319	gingival:	n/a
29	chr2:188312833-188312883	PFSK-1	brain:	n/a
30	chr2:188312833-188312883	HCPEpiC	choroid plexus:	n/a
31	chr2:188312833-188312883	AoSMC	blood vessel:	n/a
32	chr2:188312833-188312883	Hepatocyte	liver:	n/a
33	chr2:188312833-188312883	HCM	heart:	n/a
34	chr2:188312833-188312883	GM19239	blood:	n/a
35	chr2:188312833-188312883	Caco-2	colon:	n/a
36	chr2:188312833-188312883	SK-N-SH_RA	brain:	n/a
37	chr2:188312833-188312883	HL-60	blood:	n/a
38	chr2:188312833-188312883	HRCEpiC	kidney:	n/a
39	chr2:188312833-188312883	NB4	blood:	n/a
40	chr2:188312833-188312883	U87	brain:	n/a
41	chr2:188312833-188312883	HIPEpiC	eye:	n/a
42	chr2:188312833-188312883	ProgFib	skin:	n/a
43	chr2:188312833-188312883	A549	lung:	n/a
44	chr2:188312833-188312883	SAEC	small airway:	n/a
45	chr2:188312833-188312883	MCF-7	breast:	n/a
46	chr2:188312833-188312883	GM12878	blood:	n/a
47	chr2:188312833-188312883	PANC-1	pancreas:	n/a
48	chr2:188312833-188312883	AG10803	skin:	n/a
49	chr2:188312833-188312883	PrEC	prostate:	n/a
50	chr2:188312833-188312883	CMK	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr2:188325986..188328358-chr2:188338477..188341086,2	K562	blood:
2	chr2:188302851..188305687-chr2:188602438..188604231,2	K562	blood:
3	chr2:188332292..188334574-chr2:188338658..188340896,2	K562	blood:
4	chr2:187727496..187728175-chr2:188317935..188318450,2	K562	blood:
5	chr2:188163616..188164504-chr2:188317553..188318396,2	MCF-7	breast:
6	chr2:188321031..188323033-chr2:188323409..188324944,2	MCF-7	breast:
7	chr2:188313751..188315339-chr2:188318942..188321717,2	K562	blood:
8	chr2:188330316..188331975-chr2:188335329..188337023,2	K562	blood:
9	chr2:188313751..188315339-chr2:188318942..188321717,2	K562	blood:
10	chr2:188327729..188329305-chr2:188335653..188337277,2	K562	blood:
11	chr2:188330316..188331975-chr2:188335329..188337023,2	K562	blood:
12	chr2:188307594..188309818-chr2:188311954..188314639,2	K562	blood:
13	chr2:188321031..188323033-chr2:188323409..188324944,2	MCF-7	breast:
14	chr2:188327729..188329305-chr2:188335653..188337277,2	K562	blood:
15	chr2:188338540..188341601-chr2:188345636..188349487,3	K562	blood:
16	chr2:188316887..188320656-chr2:188322905..188325832,3	K562	blood:
17	chr2:188332292..188334574-chr2:188338658..188340896,2	K562	blood:
18	chr2:188329317..188331418-chr2:188341720..188346261,4	K562	blood:
19	chr2:188163672..188164442-chr2:188307237..188307741,2	MCF-7	breast:
20	chr2:188316887..188320656-chr2:188322905..188325832,3	K562	blood:
21	chr2:188325986..188328358-chr2:188338477..188341086,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TFPI-1	chr2:188312766-188312979	NONHSAT076015
2	lnc-TFPI-1	chr2:188306650-188306786	NONHSAT076017
3	lnc-TFPI-1	chr2:188301325-188301383	NONHSAT076017
4	lnc-TFPI-1	chr2:188301325-188301383	NONHSAT076015
5	lnc-TFPI-1	chr2:188312766-188312980	NONHSAT076016
6	lnc-TFPI-1	chr2:188312766-188312979	NONHSAT076017
7	lnc-TFPI-1	chr2:188312766-188312873	NONHSAT076019
8	lnc-CALCRL-1	chr2:188328960-188330769	NONHSAT076021

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	TFPI	hsa-miR-155-5p	chr2:188329078-188329101
2	TFPI	hsa-miR-7-5p	chr2:188331101-188331124
3	TFPI	hsa-miR-7-5p	chr2:188329144-188329165
4	TFPI	hsa-miR-7-5p	chr2:188331146-188331172

Variant related genes	Relation type
CALCRL	TF binding region
CALCRL	CpG island
ENSG00000064989	chromatin interactions

Extended variants
information (count: 1319 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:1319 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546636443	chr2:188301324-188301325	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs574603859	chr2:188301544-188301545	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs541645136	chr2:188301574-188301575	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs186692193	chr2:188301609-188301610	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs190767031	chr2:188301712-188301713	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs78874009	chr2:188301729-188301730	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs545399242	chr2:188301730-188301731	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs12693469	chr2:188301732-188301733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs75410876	chr2:188301830-188301831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs201281952	chr2:188301888-188301889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs540495587	chr2:188301938-188301939	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs111346080	chr2:188301991-188301992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs529523739	chr2:188301999-188302000	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs35183625	chr2:188302053-188302054	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs550883427	chr2:188302054-188302055	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs150954717	chr2:188302126-188302127	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs569377747	chr2:188302131-188302132	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs140755246	chr2:188302137-188302138	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs551818443	chr2:188302138-188302139	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs566846647	chr2:188302153-188302154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs534163713	chr2:188302173-188302174	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs553340717	chr2:188302186-188302187	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs78357827	chr2:188302216-188302217	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs376161969	chr2:188302283-188302284	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs189180630	chr2:188302418-188302419	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs556832948	chr2:188302515-188302516	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs575306801	chr2:188302560-188302561	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs536598119	chr2:188302567-188302568	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs10203781	chr2:188302587-188302588	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs367721799	chr2:188302597-188302598	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs192872746	chr2:188302633-188302634	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs3771065	chr2:188302634-188302635	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs150120237	chr2:188302652-188302653	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs183823521	chr2:188302660-188302661	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs187971229	chr2:188302669-188302670	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs544790973	chr2:188302754-188302755	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs200761208	chr2:188302767-188302768	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs13019491	chr2:188302770-188302771	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs191799172	chr2:188302818-188302819	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs556667437	chr2:188303051-188303052	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs183660515	chr2:188303057-188303058	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs527727789	chr2:188303155-188303156	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs138594688	chr2:188303174-188303175	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs114962274	chr2:188303213-188303214	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs543345235	chr2:188303219-188303220	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs141162435	chr2:188303262-188303263	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs571348923	chr2:188303270-188303271	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs77032380	chr2:188303281-188303282	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs147004496	chr2:188303319-188303320	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs371932216	chr2:188303326-188303327	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:52)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD
early-passage human iPS cells	21368824	CNVD
Tetralogy of Fallot	22912587	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:482 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:188269600-188309800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr2:188269800-188308400	Weak transcription	Primary hematopoietic stem cells	blood
3	chr2:188286600-188304000	Weak transcription	Psoas Muscle	Psoas
4	chr2:188295000-188303000	Weak transcription	Brain Substantia Nigra	brain
5	chr2:188295200-188309600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr2:188295400-188303000	Weak transcription	HSMMtube	muscle
7	chr2:188295600-188302400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr2:188295600-188302600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr2:188298400-188303000	Weak transcription	Liver	Liver
10	chr2:188298400-188303200	Weak transcription	Adipose Nuclei	Adipose
11	chr2:188298800-188301400	Enhancers	NHDF-Ad	bronchial
12	chr2:188299200-188311800	Weak transcription	Left Ventricle	heart
13	chr2:188299600-188302800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr2:188299800-188301600	Genic enhancers	HUVEC	blood vessel
15	chr2:188300200-188303200	Weak transcription	Ovary	ovary
16	chr2:188300200-188312200	Weak transcription	NHLF	lung
17	chr2:188300800-188303200	Weak transcription	Osteobl	bone
18	chr2:188301200-188303400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr2:188301200-188303400	Weak transcription	HSMM	muscle
20	chr2:188301400-188303200	Weak transcription	NHDF-Ad	bronchial
21	chr2:188301600-188302800	Enhancers	HUVEC	blood vessel
22	chr2:188302200-188309000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr2:188302400-188304200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr2:188302600-188303800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr2:188302600-188304000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr2:188302800-188303600	Enhancers	Brain Inferior Temporal Lobe	brain
27	chr2:188302800-188304000	Flanking Active TSS	HUVEC	blood vessel
28	chr2:188302800-188304200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr2:188303000-188303400	Enhancers	Brain Substantia Nigra	brain
30	chr2:188303000-188303600	Enhancers	Liver	Liver
31	chr2:188303000-188304000	Enhancers	Cortex derived primary cultured neurospheres	brain
32	chr2:188303200-188303400	Enhancers	NHDF-Ad	bronchial
33	chr2:188303200-188303600	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr2:188303200-188303600	Enhancers	Brain Hippocampus Middle	brain
35	chr2:188303200-188303600	Enhancers	Skeletal Muscle Male	skeletal muscle
36	chr2:188303200-188303600	Enhancers	Osteobl	bone
37	chr2:188303200-188304000	Enhancers	Adipose Nuclei	Adipose
38	chr2:188303200-188304200	Enhancers	Ovary	ovary
39	chr2:188303400-188303600	Enhancers	HSMM	muscle
40	chr2:188303400-188304000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr2:188303600-188304400	Weak transcription	HSMM	muscle
42	chr2:188303800-188310800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr2:188304000-188304400	Enhancers	HUVEC	blood vessel
44	chr2:188304000-188308800	Weak transcription	Adipose Nuclei	Adipose
45	chr2:188304200-188306400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr2:188304200-188311200	Weak transcription	Ovary	ovary
47	chr2:188304400-188305000	Flanking Active TSS	HUVEC	blood vessel
48	chr2:188305000-188306600	Transcr. at gene 5' and 3'	HUVEC	blood vessel
49	chr2:188305800-188308600	Weak transcription	Fetal Muscle Leg	muscle
50	chr2:188305800-188310800	Weak transcription	Fetal Kidney	kidney

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