Variant report

Variant	nsv1029370
Chromosome Location	chr6:114471446-114566884
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:359)
CpG islands
(count:367)
Chromatin interactive
region (count:10)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:359 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:114488706-114489732	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:114491020-114492995	HepG2	liver:	n/a	chr6:114491965-114491981 chr6:114491966-114491982
3	ARID3A	chr6:114485413-114485841	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:114480739-114481242	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:114488334-114488370	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:114493457-114494086	HepG2	liver:	n/a	n/a
7	BACH1	chr6:114524772-114524969	H1-hESC	embryonic stem cell:	n/a	n/a
8	BHLHE40	chr6:114488791-114489676	HepG2	liver:	n/a	n/a
9	BHLHE40	chr6:114481000-114481212	HepG2	liver:	n/a	n/a
10	BRCA1	chr6:114544536-114544884	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr6:114483841-114484198	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr6:114488693-114489566	HepG2	liver:	n/a	n/a
13	CEBPB	chr6:114495442-114495601	HepG2	liver:	n/a	chr6:114495493-114495504
14	CEBPB	chr6:114559287-114559863	HepG2	liver:	n/a	chr6:114559446-114559457
15	CEBPB	chr6:114483867-114484228	IMR90	lung:	n/a	n/a
16	CEBPB	chr6:114475989-114476158	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr6:114488766-114489283	HepG2	liver:	n/a	n/a
18	CEBPB	chr6:114483874-114484231	HepG2	liver:	n/a	n/a
19	CEBPB	chr6:114483880-114484203	A549	lung:	n/a	n/a
20	CEBPB	chr6:114488910-114489171	HepG2	liver:	n/a	n/a
21	CEBPB	chr6:114523645-114523954	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr6:114483881-114484215	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr6:114488836-114489307	HepG2	liver:	n/a	n/a
24	CEBPB	chr6:114483935-114484103	K562	blood:	n/a	n/a
25	CEBPB	chr6:114561965-114562339	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr6:114483863-114484244	ECC-1	luminal epithelium:	n/a	n/a
27	CEBPD	chr6:114488938-114489161	HepG2	liver:	n/a	n/a
28	CEBPZ	chr6:114488336-114488359	HepG2	liver:	n/a	n/a
29	CHD2	chr6:114476076-114476266	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr6:114488904-114489334	HepG2	liver:	n/a	n/a
31	CTCF	chr6:114489300-114489450	HepG2	liver:	n/a	chr6:114489397-114489406
32	CTCF	chr6:114497360-114497510	Caco-2	colon:	n/a	n/a
33	CTCF	chr6:114479160-114479310	BE2_C	brain:	n/a	n/a
34	CTCF	chr6:114486439-114486548	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr6:114486371-114486582	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr6:114490860-114491010	HMEC	breast:	n/a	chr6:114490913-114490934 chr6:114490911-114490929
37	CTCF	chr6:114479220-114479236	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr6:114552470-114552500	Pancreas_OC	pancreas:	n/a	n/a
39	CTCF	chr6:114479204-114479280	MCF-7	breast:	n/a	n/a
40	CTCF	chr6:114479196-114479270	HepG2	liver:	n/a	n/a
41	CTCF	chr6:114560400-114560550	HEK293	kidney:	n/a	n/a
42	CTCF	chr6:114473164-114473204	GM13976	blood:	n/a	n/a
43	CTCF	chr6:114489280-114489430	Caco-2	colon:	n/a	chr6:114489397-114489406
44	CTCF	chr6:114538120-114538270	AG09309	skin:	n/a	n/a
45	CTCF	chr6:114506522-114506565	GM20000	blood:	n/a	n/a
46	CTCF	chr6:114479205-114479283	MCF-7	breast:	n/a	n/a
47	CTCF	chr6:114479142-114479270	HepG2	liver:	n/a	n/a
48	CTCF	chr6:114479209-114479305	MCF-7	breast:	n/a	n/a
49	E2F4	chr6:114529521-114529681	MCF10A-Er-Src	breast:	n/a	n/a
50	E2F4	chr6:114530470-114530657	MCF10A-Er-Src	breast:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:114544140-114544190	NT2-D1	testis:	n/a
2	chr6:114544140-114544190	NT2-D1	testis:	n/a
3	chr6:114551190-114551240	AG04449	skin:	fetal
4	chr6:114524946-114524996	BJ	skin:	n/a
5	chr6:114515500-114515550	ECC-1	luminal epithelium:	n/a
6	chr6:114544140-114544190	HEK293	kidney:	embryo
7	chr6:114551190-114551240	NHBE	bronchial:	n/a
8	chr6:114549892-114549942	HCM	heart:	n/a
9	chr6:114549892-114549942	LNCaP	prostate:	n/a
10	chr6:114475951-114476001	GM12891	blood:	n/a
11	chr6:114515500-114515550	AG09309	skin:	n/a
12	chr6:114515500-114515550	GM06990	blood:	n/a
13	chr6:114515500-114515550	GM12892	blood:	n/a
14	chr6:114524946-114524996	PrEC	prostate:	n/a
15	chr6:114524946-114524996	Hela-S3	cervix:	n/a
16	chr6:114515500-114515550	BJ	skin:	n/a
17	chr6:114515500-114515550	Caco-2	colon:	n/a
18	chr6:114549892-114549942	IMR90	lung:	fetal
19	chr6:114515500-114515550	HRPEpiC	eye:	n/a
20	chr6:114524946-114524996	H1-hESC	embryonic stem cell:	embryo
21	chr6:114549892-114549942	GM12878	blood:	n/a
22	chr6:114549892-114549942	PFSK-1	brain:	n/a
23	chr6:114549892-114549942	NHDF-neo	bronchial:	n/a
24	chr6:114515500-114515550	AoSMC	blood vessel:	n/a
25	chr6:114475951-114476001	HRCEpiC	kidney:	n/a
26	chr6:114549892-114549942	HCT-116	colon:	n/a
27	chr6:114551190-114551240	HIPEpiC	eye:	n/a
28	chr6:114549892-114549942	HRCEpiC	kidney:	n/a
29	chr6:114524946-114524996	NB4	blood:	n/a
30	chr6:114544140-114544190	AG09319	gingival:	n/a
31	chr6:114475951-114476001	ProgFib	skin:	n/a
32	chr6:114515500-114515550	IMR90	lung:	fetal
33	chr6:114515500-114515550	HPAEpiC	pulmonary alveolar:	n/a
34	chr6:114544140-114544190	K562	blood:	n/a
35	chr6:114549892-114549942	HepG2	liver:	n/a
36	chr6:114475951-114476001	BE2_C	brain:	n/a
37	chr6:114524946-114524996	Caco-2	colon:	n/a
38	chr6:114515500-114515550	LNCaP	prostate:	n/a
39	chr6:114515500-114515550	HCT-116	colon:	n/a
40	chr6:114475951-114476001	Caco-2	colon:	n/a
41	chr6:114524946-114524996	A549	lung:	n/a
42	chr6:114475951-114476001	MCF10A-Er-Src	breast:	n/a
43	chr6:114524946-114524996	AG04449	skin:	fetal
44	chr6:114544140-114544190	SK-N-SH	brain:	n/a
45	chr6:114524946-114524996	HepG2	liver:	n/a
46	chr6:114549892-114549942	U87	brain:	n/a
47	chr6:114524946-114524996	SK-N-SH	brain:	n/a
48	chr6:114515500-114515550	SAEC	small airway:	n/a
49	chr6:114544140-114544190	HNPCEpiC	eye:	n/a
50	chr6:114475951-114476001	SK-N-SH	brain:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:114561580..114563702-chr6:114578615..114580670,2	K562	blood:
2	chr6:114548047..114550869-chr6:114555378..114557876,2	MCF-7	breast:
3	chr17:62502076..62503847-chr6:114506074..114508733,2	MCF-7	breast:
4	chr13:68241658..68242183-chr6:114561063..114561674,2	MCF-7	breast:
5	chr6:114490498..114491435-chr6:114625509..114626136,2	MCF-7	breast:
6	chr6:114548047..114550869-chr6:114555378..114557876,2	MCF-7	breast:
7	chr6:114474882..114478517-chr6:114482153..114484580,3	MCF-7	breast:
8	chr6:114554629..114558117-chr6:114558553..114561790,3	K562	blood:
9	chr6:114554629..114558117-chr6:114558553..114561790,3	K562	blood:
10	chr6:114474882..114478517-chr6:114482153..114484580,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MARCKS-5	chr6:114559937-114560160	NONHSAT114604
2	lnc-MARCKS-5	chr6:114556794-114556935	ENSG00000228624
3	lnc-MARCKS-5	chr6:114560153-114560363	ENSG00000228624
4	lnc-MARCKS-5	chr6:114500189-114500321	ENSG00000228624
5	lnc-MARCKS-5	chr6:114552512-114552605	ENSG00000228624.3
6	lnc-MARCKS-5	chr6:114556794-114556880	ENSG00000228624
7	lnc-MARCKS-5	chr6:114499817-114499884	ENSG00000228624
8	lnc-HDAC2-7	chr6:114489519-114489614	NONHSAT114602
9	lnc-MARCKS-5	chr6:114559070-114559123	NONHSAT114604
10	lnc-MARCKS-5	chr6:114556794-114556935	ENSG00000228624.3
11	lnc-MARCKS-5	chr6:114551305-114551510	ENSG00000228624
12	lnc-MARCKS-5	chr6:114551321-114551487	ENSG00000228624
13	lnc-MARCKS-5	chr6:114556794-114556935	ENSG00000228624
14	lnc-HDAC2-7	chr6:114488641-114488843	NONHSAT114602
15	lnc-MARCKS-5	chr6:114543973-114544037	NONHSAT114604
16	lnc-MARCKS-5	chr6:114500189-114500321	ENSG00000228624

No data

Variant related genes	Relation type
HS3ST5	TF binding region
ENSG00000228624	TF binding region
RNA5SP213	TF binding region
HS3ST5	CpG island
ENSG00000228624	CpG island
RNA5SP213	CpG island
ENSG00000258890	chromatin interactions
ENSG00000108654	chromatin interactions
CLIP4	miRNA target sites
RAD21	miRNA target sites
NFIB	miRNA target sites
PRKD3	miRNA target sites
HSP90B1	miRNA target sites
SNRNP48	miRNA target sites
PBXIP1	miRNA target sites
WAPAL	miRNA target sites

Extended variants
information (count: 3037 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:3037 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs374288960	chr6:114471451-114471452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs534681478	chr6:114471464-114471465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs144070894	chr6:114471503-114471504	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs75368331	chr6:114471509-114471510	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs541767980	chr6:114471585-114471586	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs556684047	chr6:114471607-114471608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs9481424	chr6:114471681-114471682	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs575890301	chr6:114471710-114471711	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs55639535	chr6:114471774-114471775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs148736957	chr6:114471837-114471838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs528688804	chr6:114471854-114471855	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs79095385	chr6:114471898-114471899	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs561815274	chr6:114471914-114471915	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs529381582	chr6:114471938-114471939	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs367627851	chr6:114471973-114471974	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs550907449	chr6:114471997-114471998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs569204288	chr6:114472067-114472068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs376322575	chr6:114472091-114472092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs530816476	chr6:114472172-114472173	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs185167277	chr6:114472183-114472184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs570778002	chr6:114472189-114472190	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs142359481	chr6:114472240-114472241	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs553212378	chr6:114472312-114472313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs568303576	chr6:114472348-114472349	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs113060737	chr6:114472350-114472351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs568115491	chr6:114472385-114472386	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs535242345	chr6:114472393-114472394	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs570758799	chr6:114472433-114472434	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs147446704	chr6:114472436-114472437	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs538602785	chr6:114472486-114472487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs139877214	chr6:114472519-114472520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs550960086	chr6:114472533-114472534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs189828048	chr6:114472552-114472553	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs558001377	chr6:114472558-114472559	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs573218878	chr6:114472578-114472579	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs540390462	chr6:114472676-114472677	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs561949837	chr6:114472696-114472697	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs574078683	chr6:114472744-114472745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs1401771	chr6:114472792-114472793	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs562876798	chr6:114472819-114472820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs540080203	chr6:114472852-114472853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs145394128	chr6:114472899-114472900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs564331584	chr6:114472933-114472934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs147742629	chr6:114472940-114472941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs138919475	chr6:114472962-114472963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs546813170	chr6:114473016-114473017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs62415763	chr6:114473044-114473045	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs535520107	chr6:114473106-114473107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs567198754	chr6:114473148-114473149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs550432588	chr6:114473149-114473150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:120)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Gastric cancer	17908304	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
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
Basal cell lymphoma	17170743	CNVD
Prostate cancer	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21785460	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Cancer	20164920	CNVD
Breast cancer	21364760	CNVD
Chordoma	21602918	CNVD
Kartagener syndrome	16639409	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Systemic lupus erythematosus	19220326	CNVD
Cancer	17160897	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Acute lymphoblastic leukemia	17229543	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Mental retardation	17621639	CNVD
Hypoplastic	20877625	CNVD
Hypotonia	20877625	CNVD
Mental retardation	20877625	CNVD
Microcephaly	20877625	CNVD
brachycephaly	20877625	CNVD
epicanthic folds	20877625	CNVD
micrognathia	20877625	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:507 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:114430800-114477800	Weak transcription	Brain Anterior Caudate	brain
2	chr6:114466800-114473800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr6:114466800-114476600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr6:114467200-114472000	Weak transcription	Hela-S3	cervix
5	chr6:114467800-114475000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr6:114468000-114471800	Weak transcription	Brain Angular Gyrus	brain
7	chr6:114468800-114475000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr6:114468800-114475400	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr6:114468800-114479800	Weak transcription	Brain Hippocampus Middle	brain
10	chr6:114470800-114478400	Weak transcription	Stomach Mucosa	stomach
11	chr6:114471200-114471800	Enhancers	HepG2	liver
12	chr6:114471400-114472600	Enhancers	Brain Cingulate Gyrus	brain
13	chr6:114471800-114472000	Enhancers	Brain Angular Gyrus	brain
14	chr6:114471800-114479200	Weak transcription	HepG2	liver
15	chr6:114472000-114472600	Enhancers	Hela-S3	cervix
16	chr6:114472000-114479800	Weak transcription	Brain Angular Gyrus	brain
17	chr6:114472600-114472800	Enhancers	Brain Inferior Temporal Lobe	brain
18	chr6:114472600-114476000	Weak transcription	Hela-S3	cervix
19	chr6:114472800-114480000	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr6:114473600-114476000	Enhancers	GM12878-XiMat	blood
21	chr6:114473800-114474200	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr6:114474200-114474400	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr6:114474200-114475400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr6:114474400-114475800	Weak transcription	HUES6 Cell Line	embryonic stem cell
25	chr6:114475000-114476200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr6:114475000-114476200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr6:114475000-114476800	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr6:114475200-114476200	Enhancers	H9 Cell Line	embryonic stem cell
29	chr6:114475400-114476200	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr6:114475400-114476400	Enhancers	H1 Cell Line	embryonic stem cell
31	chr6:114475400-114477000	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr6:114475600-114476200	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr6:114475800-114476200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr6:114475800-114476200	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr6:114475800-114476200	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr6:114475800-114476200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr6:114475800-114476200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr6:114475800-114476400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr6:114475800-114477000	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr6:114476000-114476800	Enhancers	Hela-S3	cervix
41	chr6:114476200-114479200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr6:114476200-114489400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
43	chr6:114476200-114493600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr6:114476200-114497800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr6:114476400-114488200	Weak transcription	H1 Cell Line	embryonic stem cell
46	chr6:114476400-114488800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr6:114476800-114489400	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chr6:114477000-114491800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
49	chr6:114477800-114478400	Enhancers	Brain Anterior Caudate	brain
50	chr6:114478200-114478600	Enhancers	Brain Substantia Nigra	brain

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