Variant report

Variant	nsv999408
Chromosome Location	chr3:158280085-158316431
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:423)
CpG islands
(count:917)
Chromatin interactive
region (count:19)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:423 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:158288831-158289023	HepG2	liver:	n/a	n/a
2	ATF1	chr3:158288707-158289119	K562	blood:	n/a	chr3:158288896-158288910
3	ATF3	chr3:158288798-158289061	K562	blood:	n/a	chr3:158288900-158288908 chr3:158288899-158288910 chr3:158288899-158288907 chr3:158288896-158288909 chr3:158288888-158288908 chr3:158288896-158288911 chr3:158288940-158288954 chr3:158288900-158288910 chr3:158288897-158288907 chr3:158288900-158288910 chr3:158288900-158288907 chr3:158288897-158288910 chr3:158288898-158288909 chr3:158288896-158288907
4	BHLHE40	chr3:158296588-158296601	GM12878	blood:	n/a	n/a
5	BHLHE40	chr3:158288656-158289396	K562	blood:	n/a	n/a
6	BRCA1	chr3:158288631-158289011	HepG2	liver:	n/a	n/a
7	BRCA1	chr3:158288446-158288534	H1-hESC	embryonic stem cell:	n/a	n/a
8	BRCA1	chr3:158288820-158289092	GM12878	blood:	n/a	n/a
9	BRCA1	chr3:158288767-158289388	H1-hESC	embryonic stem cell:	n/a	n/a
10	CBX3	chr3:158288527-158289669	K562	blood:	n/a	n/a
11	CBX3	chr3:158289746-158290237	K562	blood:	n/a	n/a
12	CBX3	chr3:158291568-158291926	K562	blood:	n/a	n/a
13	CBX3	chr3:158288743-158289150	K562	blood:	n/a	n/a
14	CCNT2	chr3:158288723-158289095	K562	blood:	n/a	n/a
15	CEBPB	chr3:158288697-158289043	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr3:158288740-158289047	K562	blood:	n/a	n/a
17	CEBPB	chr3:158288723-158289071	IMR90	lung:	n/a	n/a
18	CEBPB	chr3:158288740-158288969	HepG2	liver:	n/a	n/a
19	CEBPB	chr3:158296234-158296460	A549	lung:	n/a	n/a
20	CEBPB	chr3:158286171-158286386	K562	blood:	n/a	n/a
21	CHD2	chr3:158288874-158289010	HepG2	liver:	n/a	n/a
22	CHD2	chr3:158288608-158289399	K562	blood:	n/a	n/a
23	CHD2	chr3:158288645-158289280	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr3:158289990-158290115	K562	blood:	n/a	n/a
25	CHD2	chr3:158288762-158289135	GM12878	blood:	n/a	n/a
26	CREB1	chr3:158288708-158289020	A549	lung:	n/a	chr3:158288897-158288910
27	CREB1	chr3:158288652-158289242	GM12878	blood:	n/a	chr3:158288897-158288910
28	CREB1	chr3:158288713-158289167	HepG2	liver:	n/a	chr3:158288897-158288910
29	CREB1	chr3:158288664-158289137	ECC-1	luminal epithelium:	n/a	chr3:158288897-158288910
30	CREB1	chr3:158288651-158289182	H1-hESC	embryonic stem cell:	n/a	chr3:158288897-158288910
31	CREB1	chr3:158288626-158289183	HepG2	liver:	n/a	chr3:158288897-158288910
32	CREB1	chr3:158288619-158289272	A549	lung:	n/a	chr3:158288897-158288910
33	CREB1	chr3:158288642-158289327	H1-hESC	embryonic stem cell:	n/a	chr3:158288897-158288910
34	CREB1	chr3:158288549-158289377	K562	blood:	n/a	chr3:158288897-158288910
35	CREB1	chr3:158288607-158289288	K562	blood:	n/a	chr3:158288897-158288910
36	CREB1	chr3:158288638-158289201	ECC-1	luminal epithelium:	n/a	chr3:158288897-158288910
37	CTCF	chr3:158291748-158291802	HepG2	liver:	n/a	n/a
38	CTCF	chr3:158291640-158291790	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr3:158306668-158306714	GM13976	blood:	n/a	n/a
40	CTCF	chr3:158288736-158289130	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr3:158291634-158291804	A549	lung:	n/a	n/a
42	CTCF	chr3:158288932-158288936	GM19239	blood:	n/a	n/a
43	CTCF	chr3:158291622-158291847	K562	blood:	n/a	n/a
44	CTCF	chr3:158291660-158291810	HPF	lung:	n/a	n/a
45	CTCF	chr3:158291713-158291782	GM12878	blood:	n/a	n/a
46	CTCF	chr3:158291700-158291850	MCF-7	breast:	n/a	n/a
47	CTCF	chr3:158291604-158291848	MCF-7	breast:	n/a	n/a
48	CTCF	chr3:158291666-158291766	GM12892	blood:	n/a	n/a
49	CTCF	chr3:158291680-158291830	BE2_C	brain:	n/a	n/a
50	CTCF	chr3:158291680-158291830	A549	lung:	n/a	n/a

(count:917 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:158288944-158288994	HPAEpiC	pulmonary alveolar:	n/a
2	chr3:158288892-158288942	PFSK-1	brain:	n/a
3	chr3:158288944-158288994	HPAEpiC	pulmonary alveolar:	n/a
4	chr3:158288892-158288942	PFSK-1	brain:	n/a
5	chr3:158288706-158288756	SAEC	small airway:	n/a
6	chr3:158289061-158289111	ProgFib	skin:	n/a
7	chr3:158288944-158288994	CMK	blood:	n/a
8	chr3:158286552-158286602	HRCEpiC	kidney:	n/a
9	chr3:158289160-158289210	HCT-116	colon:	n/a
10	chr3:158288892-158288942	HepG2	liver:	n/a
11	chr3:158290728-158290778	NT2-D1	testis:	n/a
12	chr3:158288837-158288887	K562	blood:	n/a
13	chr3:158288680-158288730	RPTEC	kidney:	n/a
14	chr3:158288680-158288730	SKMC	muscle:	n/a
15	chr3:158289160-158289210	HIPEpiC	eye:	n/a
16	chr3:158288887-158288937	RPTEC	kidney:	n/a
17	chr3:158288706-158288756	MCF-7	breast:	n/a
18	chr3:158288903-158288953	MCF10A-Er-Src	breast:	n/a
19	chr3:158289061-158289111	A549	lung:	n/a
20	chr3:158288958-158289008	HepG2	liver:	n/a
21	chr3:158288837-158288887	ovcar-3	ovarian:	n/a
22	chr3:158288944-158288994	GM12891	blood:	n/a
23	chr3:158288872-158288922	CMK	blood:	n/a
24	chr3:158288958-158289008	GM12892	blood:	n/a
25	chr3:158288680-158288730	HPAEpiC	pulmonary alveolar:	n/a
26	chr3:158288944-158288994	T-47D	breast:	n/a
27	chr3:158288958-158289008	HNPCEpiC	eye:	n/a
28	chr3:158288887-158288937	AG04449	skin:	fetal
29	chr3:158288837-158288887	PANC-1	pancreas:	n/a
30	chr3:158288872-158288922	SK-N-SH	brain:	n/a
31	chr3:158288892-158288942	AG09309	skin:	n/a
32	chr3:158288872-158288922	LNCaP	prostate:	n/a
33	chr3:158288944-158288994	HIPEpiC	eye:	n/a
34	chr3:158288680-158288730	HEK293	kidney:	embryo
35	chr3:158288706-158288756	HPAEpiC	pulmonary alveolar:	n/a
36	chr3:158289160-158289210	HEK293	kidney:	embryo
37	chr3:158288887-158288937	HAEpiC	amniotic membrane:	n/a
38	chr3:158288887-158288937	PANC-1	pancreas:	n/a
39	chr3:158315980-158316030	GM12878	blood:	n/a
40	chr3:158288837-158288887	AG04450	lung:	fetal
41	chr3:158288944-158288994	SK-N-MC	brain:	n/a
42	chr3:158288680-158288730	HCT-116	colon:	n/a
43	chr3:158289061-158289111	SK-N-MC	brain:	n/a
44	chr3:158286552-158286602	PFSK-1	brain:	n/a
45	chr3:158286552-158286602	Hepatocyte	liver:	n/a
46	chr3:158288872-158288922	HNPCEpiC	eye:	n/a
47	chr3:158288958-158289008	HEEpiC	esophagus:	n/a
48	chr3:158288892-158288942	ovcar-3	ovarian:	n/a
49	chr3:158290728-158290778	HCM	heart:	n/a
50	chr3:158288706-158288756	HRPEpiC	eye:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:158291274..158292230-chr3:158361860..158362583,3	MCF-7	breast:
2	chr3:158257580..158259389-chr3:158289106..158290845,2	K562	blood:
3	chr3:158280301..158281909-chr3:158440883..158442429,2	MCF-7	breast:
4	chr3:158305166..158306893-chr3:158310417..158313351,2	K562	blood:
5	chr3:158278970..158280911-chr3:158284194..158285901,2	K562	blood:
6	chr3:158278970..158280911-chr3:158284194..158285901,2	K562	blood:
7	chr3:158310156..158311938-chr3:158314605..158316847,2	K562	blood:
8	chr3:158289477..158292573-chr3:158361739..158363921,4	K562	blood:
9	chr3:158305166..158306746-chr3:158311851..158313623,2	K562	blood:
10	chr3:158284750..158291147-chr3:158359832..158364955,8	K562	blood:
11	chr3:158291924..158294331-chr3:158300946..158303373,2	K562	blood:
12	chr3:158258697..158261392-chr3:158281959..158283679,2	K562	blood:
13	chr3:158305166..158306746-chr3:158311851..158313623,2	K562	blood:
14	chr3:158305166..158306893-chr3:158310417..158313351,2	K562	blood:
15	chr3:158291924..158294331-chr3:158300946..158303373,2	K562	blood:
16	chr3:158311702..158314376-chr3:158337102..158338612,2	K562	blood:
17	chr3:158257580..158259170-chr3:158289106..158290622,2	K562	blood:
18	chr3:158298751..158301229-chr3:158359663..158362148,3	K562	blood:
19	chr3:158310156..158311938-chr3:158314605..158316847,2	K562	blood:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LXN-3	chr3:158282151-158283758	ucscGeneNc_uc003fbc_2
2	lnc-LXN-1	chr3:158285749-158285845	NONHSAT092926
3	lnc-LXN-1	chr3:158287960-158288130	NONHSAT092926
4	lnc-LXN-3	chr3:158303841-158303962	ucscGeneNc_uc003fbc_2
5	lnc-LXN-3	chr3:158302418-158302575	ucscGeneNc_uc003fbc_2
6	lnc-RSRC1-1	chr3:158301149-158301620	l_2518_chr3:158290245-158301620_heart
7	lnc-RSRC1-1	chr3:158290246-158290605	l_2518_chr3:158290245-158301620_heart
8	lnc-LXN-1	chr3:158287960-158288855	ENSG00000243150
9	lnc-LXN-1	chr3:158287960-158288012	NONHSAT092927
10	lnc-LXN-1	chr3:158285749-158285845	ENSG00000243150
11	lnc-MLF1-1	chr3:158282277-158283401	l_2517_chr3:158282276-158289024_testes
12	lnc-MLF1-1	chr3:158288342-158288499	l_2517_chr3:158282276-158289024_testes
13	lnc-LXN-1	chr3:158285749-158285845	NONHSAT092927
14	lnc-LXN-1	chr3:158288558-158288858	NONHSAT092927
15	lnc-RSRC1-1	chr3:158299962-158300064	l_2518_chr3:158290245-158301620_heart
16	lnc-MLF1-1	chr3:158288770-158289024	l_2517_chr3:158282276-158289024_testes

No data

Variant related genes	Relation type
ENSG00000243150	TF binding region
MLF1	TF binding region
ENSG00000243150	CpG island
MLF1	CpG island
ENSG00000168827	chromatin interactions
MDM4	miRNA target sites
RAB8B	miRNA target sites

Extended variants
information (count: 1355 )
Associated
traits (count: 50 )

Variant overlapped rSNPs/rCNVs (count:1355 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1656369	chr3:158280085-158280086	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs543639399	chr3:158280087-158280088	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs184587234	chr3:158280109-158280110	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs149021457	chr3:158280127-158280128	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs142067541	chr3:158280133-158280134	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs151324183	chr3:158280203-158280204	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs545967060	chr3:158280206-158280207	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs527671571	chr3:158280229-158280230	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs114679435	chr3:158280249-158280250	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs111486275	chr3:158280312-158280313	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs561423781	chr3:158280502-158280503	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs35076982	chr3:158280538-158280539	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs188952601	chr3:158280587-158280588	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs549923094	chr3:158280593-158280594	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs181521884	chr3:158280600-158280601	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs553583388	chr3:158280604-158280605	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs538320464	chr3:158280668-158280669	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs577388558	chr3:158280714-158280715	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs547067326	chr3:158280756-158280757	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs186698286	chr3:158280794-158280795	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs535860352	chr3:158280875-158280876	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs189571333	chr3:158280916-158280917	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs140653305	chr3:158280940-158280941	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs562835790	chr3:158280966-158280967	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs537250408	chr3:158280997-158280998	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs1656368	chr3:158281021-158281022	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs180924314	chr3:158281098-158281099	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs545554455	chr3:158281119-158281120	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs560376702	chr3:158281149-158281150	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs185797397	chr3:158281155-158281156	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs368214929	chr3:158281220-158281221	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs571375094	chr3:158281275-158281276	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs190960470	chr3:158281297-158281298	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs557278008	chr3:158281302-158281303	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs561635665	chr3:158281307-158281308	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs531851006	chr3:158281385-158281386	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs145778519	chr3:158281410-158281411	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs565881875	chr3:158281426-158281427	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs565166892	chr3:158281439-158281440	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs138386402	chr3:158281472-158281473	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs141359737	chr3:158281618-158281619	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs183148673	chr3:158281625-158281626	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs34629395	chr3:158281711-158281712	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs145028294	chr3:158281734-158281735	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs547831413	chr3:158281745-158281746	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs569946368	chr3:158281768-158281769	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs536190540	chr3:158281781-158281782	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs558867573	chr3:158281797-158281798	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs138813617	chr3:158281851-158281852	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs9834415	chr3:158281894-158281895	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:50)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Hepatocellular carcinoma	16750200	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Basal cell lymphoma	17170743	CNVD
Breast cancer	16608533	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-small cell lung cancer	19010865	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16547154	CNVD
Breast cancer	21364760	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:471 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:158278600-158280200	Enhancers	Fetal Heart	heart
2	chr3:158279400-158286200	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr3:158279800-158280600	Enhancers	Left Ventricle	heart
4	chr3:158280000-158280800	Enhancers	K562	blood
5	chr3:158280200-158280400	Flanking Active TSS	Fetal Heart	heart
6	chr3:158280400-158280600	Enhancers	Fetal Heart	heart
7	chr3:158280600-158280800	Flanking Active TSS	Fetal Heart	heart
8	chr3:158280800-158282400	Enhancers	Fetal Heart	heart
9	chr3:158282400-158285000	Weak transcription	Fetal Heart	heart
10	chr3:158284000-158284400	Enhancers	NHEK	skin
11	chr3:158284200-158284600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr3:158284200-158284600	Enhancers	Psoas Muscle	Psoas
13	chr3:158284400-158288000	Weak transcription	Brain Angular Gyrus	brain
14	chr3:158284400-158288400	Weak transcription	NHEK	skin
15	chr3:158284600-158288400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr3:158284600-158288400	Weak transcription	Psoas Muscle	Psoas
17	chr3:158285000-158288400	Enhancers	Fetal Heart	heart
18	chr3:158286200-158286400	Enhancers	Skeletal Muscle Female	skeletal muscle
19	chr3:158286200-158286400	Enhancers	HUVEC	blood vessel
20	chr3:158286400-158287600	Weak transcription	Skeletal Muscle Female	skeletal muscle
21	chr3:158286600-158288400	Weak transcription	HUVEC	blood vessel
22	chr3:158286800-158287000	Enhancers	A549	lung
23	chr3:158286800-158287800	Enhancers	Right Ventricle	heart
24	chr3:158287000-158288200	Enhancers	Skeletal Muscle Male	skeletal muscle
25	chr3:158287200-158288200	Weak transcription	A549	lung
26	chr3:158287600-158287800	Enhancers	Fetal Muscle Trunk	muscle
27	chr3:158287600-158287800	Enhancers	Left Ventricle	heart
28	chr3:158287600-158288400	Enhancers	Fetal Muscle Leg	muscle
29	chr3:158287600-158288400	Enhancers	Skeletal Muscle Female	skeletal muscle
30	chr3:158287600-158288400	Enhancers	K562	blood
31	chr3:158287800-158288200	Enhancers	Brain Hippocampus Middle	brain
32	chr3:158287800-158288200	Enhancers	Ovary	ovary
33	chr3:158287800-158288400	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr3:158287800-158288400	Enhancers	Fetal Lung	lung
35	chr3:158287800-158288400	Weak transcription	Right Ventricle	heart
36	chr3:158287800-158288600	Weak transcription	Left Ventricle	heart
37	chr3:158288000-158288200	Enhancers	Brain Anterior Caudate	brain
38	chr3:158288000-158288200	Enhancers	Colon Smooth Muscle	Colon
39	chr3:158288000-158288200	Enhancers	Stomach Smooth Muscle	stomach
40	chr3:158288000-158288400	Enhancers	Brain Angular Gyrus	brain
41	chr3:158288000-158288400	Enhancers	Brain Cingulate Gyrus	brain
42	chr3:158288200-158288400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr3:158288200-158288400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr3:158288200-158288400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr3:158288200-158288400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr3:158288200-158288400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr3:158288200-158288400	Enhancers	Muscle Satellite Cultured Cells	--
48	chr3:158288200-158288400	Enhancers	Cortex derived primary cultured neurospheres	brain
49	chr3:158288200-158288400	Enhancers	Brain Inferior Temporal Lobe	brain
50	chr3:158288200-158288400	Enhancers	Fetal Brain Female	brain

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