Variant report

Variant	nsv605340
Chromosome Location	chr6:167611757-167783664
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2697)
CpG islands
(count:4332)
Chromatin interactive
region (count:33)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2697 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:167651727-167651738	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:167633428-167633974	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:167637599-167638030	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:167652605-167653007	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:167722138-167722657	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:167629415-167629646	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:167762709-167763005	HepG2	liver:	n/a	n/a
8	ARID3A	chr6:167624462-167624811	HepG2	liver:	n/a	n/a
9	ARID3A	chr6:167628930-167629130	HepG2	liver:	n/a	n/a
10	ARID3A	chr6:167754780-167756165	HepG2	liver:	n/a	n/a
11	ARID3A	chr6:167632046-167632420	HepG2	liver:	n/a	n/a
12	ARID3A	chr6:167645950-167646149	HepG2	liver:	n/a	n/a
13	ARID3A	chr6:167723215-167724601	HepG2	liver:	n/a	n/a
14	ARID3A	chr6:167699867-167700232	HepG2	liver:	n/a	n/a
15	ARID3A	chr6:167682223-167682912	HepG2	liver:	n/a	n/a
16	ARID3A	chr6:167702230-167702578	HepG2	liver:	n/a	n/a
17	ARID3A	chr6:167629887-167630151	HepG2	liver:	n/a	n/a
18	ARID3A	chr6:167655013-167655211	HepG2	liver:	n/a	n/a
19	ARID3A	chr6:167704338-167705733	HepG2	liver:	n/a	n/a
20	ATF1	chr6:167727339-167727444	K562	blood:	n/a	n/a
21	ATF1	chr6:167702337-167702425	K562	blood:	n/a	n/a
22	ATF2	chr6:167626020-167626431	GM12878	blood:	n/a	n/a
23	ATF2	chr6:167625939-167626508	GM12878	blood:	n/a	n/a
24	ATF2	chr6:167641333-167641936	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF2	chr6:167764810-167765270	H1-hESC	embryonic stem cell:	n/a	n/a
26	ATF2	chr6:167764830-167765266	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF2	chr6:167641353-167641826	H1-hESC	embryonic stem cell:	n/a	n/a
28	ATF2	chr6:167651500-167652487	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr6:167641591-167641850	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr6:167637370-167637829	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr6:167702257-167702472	H1-hESC	embryonic stem cell:	n/a	n/a
32	BACH1	chr6:167631950-167632087	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr6:167754224-167754403	H1-hESC	embryonic stem cell:	n/a	n/a
34	BACH1	chr6:167764960-167765154	H1-hESC	embryonic stem cell:	n/a	n/a
35	BATF	chr6:167631870-167632155	GM12878	blood:	n/a	n/a
36	BATF	chr6:167764807-167765183	GM12878	blood:	n/a	n/a
37	BATF	chr6:167726053-167726251	GM12878	blood:	n/a	n/a
38	BATF	chr6:167726056-167726329	GM12878	blood:	n/a	n/a
39	BATF	chr6:167702166-167702414	GM12878	blood:	n/a	n/a
40	BATF	chr6:167765430-167765771	GM12878	blood:	n/a	n/a
41	BATF	chr6:167625959-167626402	GM12878	blood:	n/a	n/a
42	BATF	chr6:167765440-167765736	GM12878	blood:	n/a	n/a
43	BATF	chr6:167625794-167626502	GM12878	blood:	n/a	n/a
44	BCL11A	chr6:167626130-167626424	GM12878	blood:	n/a	n/a
45	BCL3	chr6:167710341-167710705	GM12878	blood:	n/a	n/a
46	BCLAF1	chr6:167764829-167765189	GM12878	blood:	n/a	chr6:167764879-167764888 chr6:167765036-167765044
47	BHLHE40	chr6:167626013-167626185	GM12878	blood:	n/a	n/a
48	BHLHE40	chr6:167617588-167617796	HepG2	liver:	n/a	n/a
49	BHLHE40	chr6:167699851-167700081	HepG2	liver:	n/a	n/a
50	BHLHE40	chr6:167631891-167632258	HepG2	liver:	n/a	n/a

(count:4332 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:167770239-167770289	SK-N-MC	brain:	n/a
2	chr6:167770239-167770289	SK-N-MC	brain:	n/a
3	chr6:167653957-167654007	HCT-116	colon:	n/a
4	chr6:167763975-167764025	HCM	heart:	n/a
5	chr6:167703894-167703944	GM06990	blood:	n/a
6	chr6:167622202-167622252	T-47D	breast:	n/a
7	chr6:167709720-167709770	HCPEpiC	choroid plexus:	n/a
8	chr6:167695026-167695076	NHBE	bronchial:	n/a
9	chr6:167738277-167738327	SK-N-SH_RA	brain:	n/a
10	chr6:167704769-167704819	PANC-1	pancreas:	n/a
11	chr6:167655290-167655340	AoSMC	blood vessel:	n/a
12	chr6:167680455-167680505	SK-N-MC	brain:	n/a
13	chr6:167649539-167649589	A549	lung:	n/a
14	chr6:167709237-167709287	AG04449	skin:	fetal
15	chr6:167653957-167654007	NT2-D1	testis:	n/a
16	chr6:167653907-167653957	H1-hESC	embryonic stem cell:	embryo
17	chr6:167705750-167705800	GM12892	blood:	n/a
18	chr6:167655290-167655340	LNCaP	prostate:	n/a
19	chr6:167704673-167704723	HPAEpiC	pulmonary alveolar:	n/a
20	chr6:167616968-167617018	HRE	kidney:	n/a
21	chr6:167680447-167680497	RPTEC	kidney:	n/a
22	chr6:167704673-167704723	NHDF-neo	bronchial:	n/a
23	chr6:167704808-167704858	GM19239	blood:	n/a
24	chr6:167763758-167763808	PrEC	prostate:	n/a
25	chr6:167765215-167765265	HRCEpiC	kidney:	n/a
26	chr6:167709237-167709287	SK-N-MC	brain:	n/a
27	chr6:167655053-167655103	LNCaP	prostate:	n/a
28	chr6:167763320-167763370	PrEC	prostate:	n/a
29	chr6:167761204-167761254	PFSK-1	brain:	n/a
30	chr6:167655053-167655103	HNPCEpiC	eye:	n/a
31	chr6:167649539-167649589	Hela-S3	cervix:	n/a
32	chr6:167756099-167756149	LNCaP	prostate:	n/a
33	chr6:167633955-167634005	AG10803	skin:	n/a
34	chr6:167739618-167739668	Jurkat	blood:	n/a
35	chr6:167652028-167652078	Hela-S3	cervix:	n/a
36	chr6:167763819-167763869	A549	lung:	n/a
37	chr6:167704673-167704723	H1-hESC	embryonic stem cell:	embryo
38	chr6:167700000-167700050	HepG2	liver:	n/a
39	chr6:167763975-167764025	SK-N-MC	brain:	n/a
40	chr6:167704808-167704858	SK-N-SH_RA	brain:	n/a
41	chr6:167622441-167622491	GM12878	blood:	n/a
42	chr6:167763975-167764025	HNPCEpiC	eye:	n/a
43	chr6:167764523-167764573	HNPCEpiC	eye:	n/a
44	chr6:167764146-167764196	CMK	blood:	n/a
45	chr6:167634139-167634189	HAEpiC	amniotic membrane:	n/a
46	chr6:167633022-167633072	Hepatocyte	liver:	n/a
47	chr6:167617119-167617169	SK-N-SH	brain:	n/a
48	chr6:167634139-167634189	LNCaP	prostate:	n/a
49	chr6:167680455-167680505	HCT-116	colon:	n/a
50	chr6:167704769-167704819	GM12878	blood:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:167703616..167705764-chr6:167717598..167719278,2	MCF-7	breast:
2	chr6:167615262..167616947-chr6:167733556..167735117,2	MCF-7	breast:
3	chr6:167631751..167632287-chr6:167701939..167702527,2	MCF-7	breast:
4	chr6:167734899..167737753-chr6:167743376..167745822,2	MCF-7	breast:
5	chr1:28836187..28837925-chr6:167694572..167696254,2	K562	blood:
6	chr6:167636874..167638495-chr6:167694115..167696567,2	K562	blood:
7	chr6:167631565..167632072-chr6:167702069..167702692,3	K562	blood:
8	chr6:167615262..167616947-chr6:167733556..167735117,2	MCF-7	breast:
9	chr6:167734899..167737753-chr6:167743376..167745822,2	MCF-7	breast:
10	chr6:167715327..167717333-chr6:167717541..167719931,2	MCF-7	breast:
11	chr6:167736614..167738249-chr6:167740426..167742938,2	K562	blood:
12	chr6:167668192..167671777-chr6:167684157..167687082,3	K562	blood:
13	chr6:167743283..167745523-chr6:167751106..167753120,2	K562	blood:
14	chr6:167744023..167747282-chr6:167750789..167753119,3	K562	blood:
15	chr6:167623779..167626117-chr6:167629928..167632260,2	MCF-7	breast:
16	chr6:167702039..167702568-chr6:167764606..167765474,2	MCF-7	breast:
17	chr6:167662732..167663315-chr6:167819023..167819880,2	K562	blood:
18	chr6:167631565..167632072-chr6:167702069..167702692,3	K562	blood:
19	chr6:167662535..167665478-chr6:167668701..167671430,2	K562	blood:
20	chr6:167744023..167747282-chr6:167750789..167753119,3	K562	blood:
21	chr6:167187967..167188932-chr6:167764453..167765086,2	K562	blood:
22	chr6:167715327..167717333-chr6:167717541..167719931,2	MCF-7	breast:
23	chr6:167699179..167702166-chr6:167703091..167705361,2	K562	blood:
24	chr6:167623779..167626117-chr6:167629928..167632260,2	MCF-7	breast:
25	chr6:167636874..167638495-chr6:167694115..167696567,2	K562	blood:
26	chr6:167620399..167623068-chr6:167623897..167626646,2	K562	blood:
27	chr6:167736614..167738249-chr6:167740426..167742938,2	K562	blood:
28	chr6:167662535..167665478-chr6:167668701..167671430,2	K562	blood:
29	chr6:167669951..167671777-chr6:167683631..167687000,3	K562	blood:
30	chr6:167631751..167632287-chr6:167701939..167702527,2	MCF-7	breast:
31	chr6:167623945..167626187-chr6:168297648..168300373,2	K562	blood:
32	chr6:167743283..167745523-chr6:167751106..167753120,2	K562	blood:
33	chr6:167702039..167702568-chr6:167764606..167765474,2	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPR31-1	chr6:167651156-167651293	XLOC_005921
2	lnc-GPR31-1	chr6:167650996-167651293	XLOC_005921
3	lnc-UNC93A-2	chr6:167760960-167761541	NONHSAT116094
4	lnc-GPR31-1	chr6:167653688-167653968	XLOC_005921
5	lnc-UNC93A-3	chr6:167764976-167765446	NONHSAT116095
6	lnc-UNC93A-3	chr6:167764293-167764966	NONHSAT116095
7	lnc-UNC93A-1	chr6:167655379-167655453	XLOC_005540
8	lnc-UNC93A-1	chr6:167659275-167659404	XLOC_005540
9	lnc-GPR31-1	chr6:167653636-167653833	XLOC_005921

No data

Variant related genes	Relation type
UNC93A	TF binding region
TTLL2	TF binding region
ENSG00000231720	TF binding region
ENSG00000228648	TF binding region
ENSG00000216966	TF binding region
ENSG00000217447	TF binding region
UNC93A	CpG island
TTLL2	CpG island
ENSG00000231720	CpG island
ENSG00000228648	CpG island
ENSG00000216966	CpG island
ENSG00000217447	CpG island
ENSG00000112494	chromatin interactions
ENSG00000180198	chromatin interactions
ENSG00000216966	chromatin interactions
CYBASC3	miRNA target sites
CYB5R4	miRNA target sites

Extended variants
information (count: 8469 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:8469 , 50 per page) page: 1 2 3 4 5 6 7 ... 170

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9347182	chr6:167611757-167611758	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs532141191	chr6:167611779-167611780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs150011395	chr6:167611815-167611816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs192894652	chr6:167611849-167611850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs553819403	chr6:167611869-167611870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs185037243	chr6:167611883-167611884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs539108307	chr6:167611888-167611889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs537384729	chr6:167611935-167611936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs546082818	chr6:167611990-167611991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs558066056	chr6:167611997-167611998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs573142020	chr6:167612004-167612005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs188608622	chr6:167612036-167612037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs547555419	chr6:167612058-167612059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs561931356	chr6:167612066-167612067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs555321613	chr6:167612130-167612131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs147262738	chr6:167612170-167612171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs7747125	chr6:167612184-167612185	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs191526137	chr6:167612204-167612205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs140735248	chr6:167612216-167612217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs144644501	chr6:167612268-167612269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs183864998	chr6:167612271-167612272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs372409439	chr6:167612272-167612273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs528028842	chr6:167612312-167612313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs374412038	chr6:167612335-167612336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs549269694	chr6:167612345-167612346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs567850561	chr6:167612374-167612375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs147872281	chr6:167612385-167612386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs556707865	chr6:167612396-167612397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs571800397	chr6:167612446-167612447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs539035280	chr6:167612464-167612465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs12055665	chr6:167612479-167612480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs554250677	chr6:167612491-167612492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs377309667	chr6:167612497-167612498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs573016250	chr6:167612500-167612501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs112495770	chr6:167612508-167612509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs545973354	chr6:167612530-167612531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs188161132	chr6:167612539-167612540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs73027318	chr6:167612574-167612575	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs544037109	chr6:167612583-167612584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs9459910	chr6:167612613-167612614	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs11967077	chr6:167612617-167612618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs550126266	chr6:167612621-167612622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs544594236	chr6:167612647-167612648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs560102056	chr6:167612655-167612656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs527931841	chr6:167612661-167612662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs182438684	chr6:167612675-167612676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs113198855	chr6:167612763-167612764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs561288143	chr6:167612810-167612811	Active TSS Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs531923389	chr6:167612812-167612813	Active TSS Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs550422206	chr6:167612843-167612844	Active TSS Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
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
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
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	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
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Testicular germ cell tumor	18059402	CNVD
Chordoma	18071362	CNVD
Glioblastoma multiforme	19435819	CNVD
Developmental delay	21147756	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Epilepsy	22083797	CNVD
Myelofibrosis	22110671	CNVD
chordoma	19801981	CNVD
Myxofibrosarcoma	16751306	CNVD
Autism	17483303	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute myeloid leukemia	19651601	CNVD
Sudden cardiac death	19188705	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1831 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:167610600-167615400	Weak transcription	Fetal Brain Male	brain
2	chr6:167610800-167612800	Weak transcription	Fetal Intestine Small	intestine
3	chr6:167611000-167613000	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr6:167612800-167613000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr6:167612800-167615000	Strong transcription	Fetal Intestine Small	intestine
6	chr6:167613000-167613600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr6:167613000-167613800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr6:167613000-167616600	Enhancers	Placenta Amnion	Placenta Amnion
9	chr6:167613600-167613800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr6:167613800-167614400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr6:167613800-167622200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr6:167614000-167615400	Enhancers	HepG2	liver
13	chr6:167614200-167614400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr6:167614400-167614800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr6:167614400-167623200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr6:167614800-167616400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr6:167615000-167616800	Weak transcription	Fetal Intestine Small	intestine
18	chr6:167615400-167616400	Weak transcription	HepG2	liver
19	chr6:167615400-167617400	Enhancers	Fetal Brain Male	brain
20	chr6:167615800-167616200	Enhancers	Fetal Lung	lung
21	chr6:167615800-167628800	Weak transcription	Right Atrium	heart
22	chr6:167616400-167617000	Enhancers	HepG2	liver
23	chr6:167616400-167617400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr6:167616400-167617600	Enhancers	Rectal Smooth Muscle	rectum
25	chr6:167616600-167617200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr6:167616600-167617800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr6:167616600-167618400	Weak transcription	Placenta Amnion	Placenta Amnion
28	chr6:167616800-167617200	Enhancers	Stomach Smooth Muscle	stomach
29	chr6:167616800-167617400	Bivalent Enhancer	K562	blood
30	chr6:167616800-167617600	Enhancers	Fetal Intestine Small	intestine
31	chr6:167617000-167617400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr6:167617000-167617400	Enhancers	Liver	Liver
33	chr6:167617000-167617400	Enhancers	Fetal Heart	heart
34	chr6:167617000-167617400	Enhancers	Fetal Intestine Large	intestine
35	chr6:167617000-167617400	Enhancers	Lung	lung
36	chr6:167617000-167617400	Active TSS	A549	lung
37	chr6:167617000-167617400	Flanking Active TSS	HepG2	liver
38	chr6:167617000-167617400	Enhancers	NH-A	brain
39	chr6:167617200-167617400	Enhancers	Colon Smooth Muscle	Colon
40	chr6:167617200-167617400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
41	chr6:167617400-167618200	Weak transcription	NH-A	brain
42	chr6:167617400-167618600	Weak transcription	Fetal Brain Male	brain
43	chr6:167617400-167619000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr6:167617400-167620800	Enhancers	HepG2	liver
45	chr6:167617400-167622400	Weak transcription	Fetal Intestine Large	intestine
46	chr6:167617600-167618000	Weak transcription	Fetal Intestine Small	intestine
47	chr6:167617600-167618000	Weak transcription	Rectal Smooth Muscle	rectum
48	chr6:167617600-167618200	Weak transcription	Colon Smooth Muscle	Colon
49	chr6:167618000-167619000	Enhancers	Fetal Intestine Small	intestine
50	chr6:167618000-167619000	Enhancers	Rectal Smooth Muscle	rectum

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