Variant report

Variant	nsv590024
Chromosome Location	chr3:28947691-29192092
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1191)
CpG islands
(count:244)
Chromatin interactive
region (count:15)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1191 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr3:28975675-28976266	GM12878	blood:	n/a	n/a
2	ATF2	chr3:28975767-28976188	GM12878	blood:	n/a	n/a
3	ATF2	chr3:28976569-28977135	GM12878	blood:	n/a	n/a
4	ATF3	chr3:28957603-28957890	H1-hESC	embryonic stem cell:	n/a	chr3:28957743-28957756
5	BACH1	chr3:28993287-28993652	K562	blood:	n/a	chr3:28993462-28993476
6	BACH1	chr3:29107009-29107265	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr3:28966571-28966750	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr3:28993198-28993922	H1-hESC	embryonic stem cell:	n/a	chr3:28993462-28993476
9	BATF	chr3:29046698-29047008	GM12878	blood:	n/a	chr3:29046864-29046875
10	BATF	chr3:29101008-29101163	GM12878	blood:	n/a	n/a
11	BATF	chr3:29024495-29024725	GM12878	blood:	n/a	chr3:29024582-29024593
12	BATF	chr3:29024462-29024701	GM12878	blood:	n/a	chr3:29024582-29024593
13	BATF	chr3:29068457-29068707	GM12878	blood:	n/a	chr3:29068605-29068616
14	BATF	chr3:29031298-29031615	GM12878	blood:	n/a	n/a
15	BATF	chr3:29067785-29068061	GM12878	blood:	n/a	n/a
16	BATF	chr3:28958230-28958538	GM12878	blood:	n/a	n/a
17	BATF	chr3:29068412-29068792	GM12878	blood:	n/a	chr3:29068605-29068616
18	BATF	chr3:29046626-29047090	GM12878	blood:	n/a	chr3:29046864-29046875
19	BATF	chr3:28965515-28965850	GM12878	blood:	n/a	chr3:28965666-28965677
20	BATF	chr3:29067772-29068072	GM12878	blood:	n/a	n/a
21	BCL11A	chr3:28982066-28982360	GM12878	blood:	n/a	n/a
22	BCL11A	chr3:28958299-28958601	GM12878	blood:	n/a	chr3:28958471-28958480
23	BCLAF1	chr3:28958158-28958630	GM12878	blood:	n/a	chr3:28958471-28958480
24	BHLHE40	chr3:29031151-29031507	GM12878	blood:	n/a	n/a
25	BRCA1	chr3:29106759-29107318	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr3:28960964-28960965	H1-hESC	embryonic stem cell:	n/a	n/a
27	CCNT2	chr3:29019093-29019184	K562	blood:	n/a	n/a
28	CEBPB	chr3:29036720-29036931	HepG2	liver:	n/a	chr3:29036867-29036878
29	CEBPB	chr3:28957577-28957932	ECC-1	luminal epithelium:	n/a	n/a
30	CEBPB	chr3:28957534-28957900	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr3:29120898-29121149	IMR90	lung:	n/a	n/a
32	CEBPB	chr3:29123669-29123898	HepG2	liver:	n/a	chr3:29123755-29123766
33	CEBPB	chr3:29179657-29180035	IMR90	lung:	n/a	chr3:29179842-29179853 chr3:29179743-29179756
34	CEBPB	chr3:29106602-29106951	ECC-1	luminal epithelium:	n/a	chr3:29106748-29106759 chr3:29106748-29106759 chr3:29106748-29106761
35	CEBPB	chr3:29064513-29064832	HepG2	liver:	n/a	chr3:29064657-29064666 chr3:29064657-29064666 chr3:29064657-29064666 chr3:29064655-29064666 chr3:29064657-29064666
36	CEBPB	chr3:28957582-28957929	A549	lung:	n/a	n/a
37	CEBPB	chr3:29179665-29180024	Hela-S3	cervix:	n/a	chr3:29179842-29179853 chr3:29179743-29179756
38	CEBPB	chr3:29091123-29091429	HepG2	liver:	n/a	n/a
39	CEBPB	chr3:29179655-29180033	A549	lung:	n/a	chr3:29179842-29179853 chr3:29179743-29179756
40	CEBPB	chr3:28957592-28957916	MCF-7	breast:	n/a	n/a
41	CEBPB	chr3:29091125-29091325	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr3:29179605-29180085	ECC-1	luminal epithelium:	n/a	chr3:29179842-29179853 chr3:29179743-29179756
43	CEBPB	chr3:29098786-29099050	IMR90	lung:	n/a	n/a
44	CEBPB	chr3:29126098-29126194	A549	lung:	n/a	n/a
45	CEBPB	chr3:28957563-28957886	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr3:29183807-29183873	H1-hESC	embryonic stem cell:	n/a	chr3:29183838-29183849
47	CEBPB	chr3:29019130-29019334	A549	lung:	n/a	chr3:29019243-29019256 chr3:29019243-29019256 chr3:29019243-29019254 chr3:29019243-29019254
48	CEBPB	chr3:29179656-29180025	H1-hESC	embryonic stem cell:	n/a	chr3:29179842-29179853 chr3:29179743-29179756
49	CEBPB	chr3:29181651-29181715	A549	lung:	n/a	n/a
50	CEBPB	chr3:29120945-29121145	HepG2	liver:	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	chr3:29182931-29182981	HCM	heart:	n/a
2	chr3:29153433-29153483	SKMC	muscle:	n/a
3	chr3:29141029-29141079	HEK293	kidney:	embryo
4	chr3:28982939-28982989	HIPEpiC	eye:	n/a
5	chr3:29182931-29182981	AoSMC	blood vessel:	n/a
6	chr3:29153433-29153483	AG10803	skin:	n/a
7	chr3:29182931-29182981	GM19239	blood:	n/a
8	chr3:29141029-29141079	ovcar-3	ovarian:	n/a
9	chr3:29141029-29141079	SAEC	small airway:	n/a
10	chr3:29153433-29153483	ProgFib	skin:	n/a
11	chr3:29141029-29141079	SKMC	muscle:	n/a
12	chr3:29141029-29141079	RPTEC	kidney:	n/a
13	chr3:28982939-28982989	A549	lung:	n/a
14	chr3:29141029-29141079	MCF10A-Er-Src	breast:	n/a
15	chr3:28982939-28982989	GM12878	blood:	n/a
16	chr3:29141029-29141079	HMEC	breast:	n/a
17	chr3:28982939-28982989	HEK293	kidney:	embryo
18	chr3:28982939-28982989	HEEpiC	esophagus:	n/a
19	chr3:28982939-28982989	MCF10A-Er-Src	breast:	n/a
20	chr3:29141029-29141079	HepG2	liver:	n/a
21	chr3:28982939-28982989	SK-N-SH	brain:	n/a
22	chr3:29182931-29182981	AG04450	lung:	fetal
23	chr3:29182931-29182981	RPTEC	kidney:	n/a
24	chr3:29182931-29182981	T-47D	breast:	n/a
25	chr3:29182931-29182981	HAEpiC	amniotic membrane:	n/a
26	chr3:28982939-28982989	NB4	blood:	n/a
27	chr3:29141029-29141079	AG09319	gingival:	n/a
28	chr3:28982939-28982989	Hela-S3	cervix:	n/a
29	chr3:29141029-29141079	Jurkat	blood:	n/a
30	chr3:29141029-29141079	Caco-2	colon:	n/a
31	chr3:29153433-29153483	RPTEC	kidney:	n/a
32	chr3:29182931-29182981	HepG2	liver:	n/a
33	chr3:28982939-28982989	AG09309	skin:	n/a
34	chr3:29182931-29182981	HMEC	breast:	n/a
35	chr3:29141029-29141079	MCF-7	breast:	n/a
36	chr3:29141029-29141079	HIPEpiC	eye:	n/a
37	chr3:29141029-29141079	CMK	blood:	n/a
38	chr3:29153433-29153483	IMR90	lung:	fetal
39	chr3:29153433-29153483	BE2_C	brain:	n/a
40	chr3:29182931-29182981	HCPEpiC	choroid plexus:	n/a
41	chr3:29153433-29153483	NHBE	bronchial:	n/a
42	chr3:28982939-28982989	HCF	heart:	n/a
43	chr3:28982939-28982989	GM12892	blood:	n/a
44	chr3:29153433-29153483	HNPCEpiC	eye:	n/a
45	chr3:29182931-29182981	A549	lung:	n/a
46	chr3:29153433-29153483	NHDF-neo	bronchial:	n/a
47	chr3:28982939-28982989	AoSMC	blood vessel:	n/a
48	chr3:29141029-29141079	PANC-1	pancreas:	n/a
49	chr3:29182931-29182981	HPAEpiC	pulmonary alveolar:	n/a
50	chr3:28982939-28982989	NHBE	bronchial:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:29164414..29165975-chr6:106497531..106500147,2	MCF-7	breast:
2	chr3:29064589..29066355-chr3:29068534..29071105,2	K562	blood:
3	chr3:29013488..29016191-chr3:29026950..29029091,2	K562	blood:
4	chr3:29081827..29084396-chr3:29087199..29088951,2	K562	blood:
5	chr3:29073333..29076176-chr3:29079165..29081520,2	K562	blood:
6	chr3:28982296..28985161-chr3:28989817..28992484,2	K562	blood:
7	chr3:28982296..28985161-chr3:28989817..28992484,2	K562	blood:
8	chr3:29064589..29066355-chr3:29068534..29071105,2	K562	blood:
9	chr3:29073333..29076176-chr3:29079165..29081520,2	K562	blood:
10	chr13:94234119..94234981-chr3:29063764..29064299,2	MCF-7	breast:
11	chr15:73783487..73784303-chr3:28967494..28967994,2	MCF-7	breast:
12	chr3:28991975..28993752-chr3:29008566..29010572,2	K562	blood:
13	chr3:29081827..29084396-chr3:29087199..29088951,2	K562	blood:
14	chr3:28991975..28993752-chr3:29008566..29010572,2	K562	blood:
15	chr3:29013488..29016191-chr3:29026950..29029091,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RBMS3-3	chr3:29128887-29130090	NONHSAT088798

No data

Variant related genes	Relation type
ENSG00000238470	TF binding region
MESTP4	TF binding region
ENSG00000238470	CpG island
MESTP4	CpG island

Extended variants
information (count: 5846 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:5846 , 50 per page) page: 1 2 3 4 5 6 7 ... 117

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9847735	chr3:28947691-28947692	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs146731207	chr3:28947697-28947698	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs578229545	chr3:28947724-28947725	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs540855312	chr3:28947741-28947742	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs376735029	chr3:28947742-28947743	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs534108052	chr3:28947748-28947749	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs140281762	chr3:28947754-28947755	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs548655891	chr3:28947761-28947762	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs562513500	chr3:28947765-28947766	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs531472809	chr3:28947782-28947783	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs551676311	chr3:28947831-28947832	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs571238553	chr3:28947855-28947856	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs557119517	chr3:28947886-28947887	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs527469940	chr3:28947897-28947898	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs574755970	chr3:28947985-28947986	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs547232969	chr3:28948032-28948033	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs192841791	chr3:28948035-28948036	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs73060069	chr3:28948053-28948054	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs555431553	chr3:28948099-28948100	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs542888664	chr3:28948158-28948159	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs73060071	chr3:28948180-28948181	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs538127174	chr3:28948200-28948201	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs558407511	chr3:28948240-28948241	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs578258288	chr3:28948249-28948250	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs66504654	chr3:28948250-28948251	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs545377120	chr3:28948269-28948270	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs565284012	chr3:28948280-28948281	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs9852364	chr3:28948289-28948290	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs550032942	chr3:28948306-28948307	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs185233358	chr3:28948387-28948388	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs562318655	chr3:28948389-28948390	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs531317161	chr3:28948417-28948418	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs563438318	chr3:28948445-28948446	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs35504513	chr3:28948458-28948459	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs550695670	chr3:28948474-28948475	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs73060075	chr3:28948555-28948556	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs549250143	chr3:28948557-28948558	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs150436896	chr3:28948563-28948564	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs188497948	chr3:28948572-28948573	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs75438676	chr3:28948595-28948596	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs114944934	chr3:28948649-28948650	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs551337683	chr3:28948770-28948771	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs571291605	chr3:28948850-28948851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs145246718	chr3:28948851-28948852	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs34142085	chr3:28948888-28948889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs398081990	chr3:28948892-28948893	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs398051737	chr3:28948893-28948894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs199885242	chr3:28948894-28948895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs149149514	chr3:28948917-28948918	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs569279454	chr3:28948926-28948927	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelofibrosis	22110671	CNVD
Lung cancer	16618734	CNVD
Cancer	20164919	CNVD
Developmental delay	21147756	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:28943800-28949000	Weak transcription	Hela-S3	cervix
2	chr3:28947000-28948800	Enhancers	Dnd41	blood
3	chr3:28948000-28948600	Enhancers	HSMM	muscle
4	chr3:28948200-28948400	Enhancers	HSMMtube	muscle
5	chr3:28948800-28949400	Enhancers	HSMMtube	muscle
6	chr3:28949000-28949800	Enhancers	Hela-S3	cervix
7	chr3:28953200-28953400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr3:28953200-28953600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr3:28953400-28956800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr3:28953600-28953800	Enhancers	Rectal Smooth Muscle	rectum
11	chr3:28953600-28954000	Active TSS	NHLF	lung
12	chr3:28953600-28954200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr3:28953600-28954200	Active TSS	Aorta	Aorta
14	chr3:28953800-28954200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr3:28953800-28954200	Active TSS	Right Atrium	heart
16	chr3:28953800-28954400	Active TSS	Fetal Lung	lung
17	chr3:28953800-28957400	Weak transcription	Rectal Smooth Muscle	rectum
18	chr3:28954000-28955000	Weak transcription	NHLF	lung
19	chr3:28954200-28957200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr3:28954200-28957200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr3:28954200-28957400	Weak transcription	Right Atrium	heart
22	chr3:28954200-28957600	Weak transcription	Aorta	Aorta
23	chr3:28954400-28955200	Weak transcription	Fetal Lung	lung
24	chr3:28954800-28957400	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr3:28955000-28955200	Enhancers	Skeletal Muscle Female	skeletal muscle
26	chr3:28955000-28955600	Enhancers	NHLF	lung
27	chr3:28955200-28956000	Enhancers	Fetal Lung	lung
28	chr3:28955200-28957200	Weak transcription	Skeletal Muscle Female	skeletal muscle
29	chr3:28955400-28955600	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr3:28955400-28955600	Enhancers	Fetal Stomach	stomach
31	chr3:28955400-28955800	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr3:28955400-28955800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr3:28955600-28957200	Weak transcription	NHLF	lung
34	chr3:28955800-28956200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr3:28955800-28959000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr3:28956000-28957200	Weak transcription	Fetal Lung	lung
37	chr3:28956200-28957400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr3:28956200-28958200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr3:28956800-28958800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr3:28957000-28957200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr3:28957000-28958600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr3:28957200-28957400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr3:28957200-28957400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr3:28957200-28957400	Enhancers	Brain Anterior Caudate	brain
45	chr3:28957200-28957400	Enhancers	Brain Hippocampus Middle	brain
46	chr3:28957200-28957400	Enhancers	Skeletal Muscle Female	skeletal muscle
47	chr3:28957200-28957400	Enhancers	NH-A	brain
48	chr3:28957200-28957400	Enhancers	NHLF	lung
49	chr3:28957200-28957400	Enhancers	Osteobl	bone
50	chr3:28957200-28957600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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