Variant report

Variant	nsv1027083
Chromosome Location	chr6:167695211-167785109
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1363)
CpG islands
(count:2505)
Chromatin interactive
region (count:20)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1363 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:167699867-167700232	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:167704338-167705733	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:167762709-167763005	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:167754780-167756165	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:167723215-167724601	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:167722138-167722657	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:167702230-167702578	HepG2	liver:	n/a	n/a
8	ATF1	chr6:167702337-167702425	K562	blood:	n/a	n/a
9	ATF1	chr6:167727339-167727444	K562	blood:	n/a	n/a
10	ATF2	chr6:167764830-167765266	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr6:167764810-167765270	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr6:167702257-167702472	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr6:167764960-167765154	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr6:167754224-167754403	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr6:167764807-167765183	GM12878	blood:	n/a	n/a
16	BATF	chr6:167765440-167765736	GM12878	blood:	n/a	n/a
17	BATF	chr6:167765430-167765771	GM12878	blood:	n/a	n/a
18	BATF	chr6:167702166-167702414	GM12878	blood:	n/a	n/a
19	BATF	chr6:167726053-167726251	GM12878	blood:	n/a	n/a
20	BATF	chr6:167726056-167726329	GM12878	blood:	n/a	n/a
21	BCL3	chr6:167710341-167710705	GM12878	blood:	n/a	n/a
22	BCLAF1	chr6:167764829-167765189	GM12878	blood:	n/a	chr6:167764879-167764888 chr6:167765036-167765044
23	BHLHE40	chr6:167723177-167724281	HepG2	liver:	n/a	n/a
24	BHLHE40	chr6:167754879-167756141	HepG2	liver:	n/a	n/a
25	BHLHE40	chr6:167722146-167722527	HepG2	liver:	n/a	n/a
26	BHLHE40	chr6:167733370-167733629	HepG2	liver:	n/a	n/a
27	BHLHE40	chr6:167702264-167702463	HepG2	liver:	n/a	n/a
28	BHLHE40	chr6:167764869-167765070	K562	blood:	n/a	n/a
29	BHLHE40	chr6:167702270-167702451	K562	blood:	n/a	n/a
30	BHLHE40	chr6:167733252-167733970	HepG2	liver:	n/a	n/a
31	BHLHE40	chr6:167732490-167732554	GM12878	blood:	n/a	n/a
32	BHLHE40	chr6:167704696-167705644	HepG2	liver:	n/a	n/a
33	BHLHE40	chr6:167722070-167722725	HepG2	liver:	n/a	chr6:167722523-167722539
34	BHLHE40	chr6:167755635-167755964	HepG2	liver:	n/a	n/a
35	BHLHE40	chr6:167723198-167723690	HepG2	liver:	n/a	n/a
36	BHLHE40	chr6:167755531-167755951	HepG2	liver:	n/a	n/a
37	BHLHE40	chr6:167764785-167765457	GM12878	blood:	n/a	n/a
38	BHLHE40	chr6:167699851-167700081	HepG2	liver:	n/a	n/a
39	BRCA1	chr6:167722055-167722521	HepG2	liver:	n/a	n/a
40	BRCA1	chr6:167750805-167750846	HepG2	liver:	n/a	n/a
41	BRCA1	chr6:167764922-167765205	H1-hESC	embryonic stem cell:	n/a	n/a
42	CBX3	chr6:167708857-167709379	K562	blood:	n/a	n/a
43	CBX3	chr6:167702109-167702642	K562	blood:	n/a	n/a
44	CBX3	chr6:167708762-167709384	K562	blood:	n/a	n/a
45	CEBPB	chr6:167722076-167722571	HepG2	liver:	n/a	n/a
46	CEBPB	chr6:167699860-167700082	HepG2	liver:	n/a	n/a
47	CEBPB	chr6:167704252-167704595	HepG2	liver:	n/a	n/a
48	CEBPB	chr6:167723191-167723562	HepG2	liver:	n/a	n/a
49	CEBPB	chr6:167705190-167705356	K562	blood:	n/a	chr6:167705263-167705276 chr6:167705265-167705274 chr6:167705263-167705274
50	CEBPB	chr6:167742112-167742401	HepG2	liver:	n/a	n/a

(count:2505 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:167763975-167764025	SK-N-MC	brain:	n/a
2	chr6:167717196-167717246	SK-N-MC	brain:	n/a
3	chr6:167705253-167705303	SKMC	muscle:	n/a
4	chr6:167703894-167703944	HCT-116	colon:	n/a
5	chr6:167763975-167764025	SK-N-MC	brain:	n/a
6	chr6:167717196-167717246	SK-N-MC	brain:	n/a
7	chr6:167705253-167705303	SKMC	muscle:	n/a
8	chr6:167703894-167703944	HCT-116	colon:	n/a
9	chr6:167770239-167770289	U87	brain:	n/a
10	chr6:167738425-167738475	GM12878	blood:	n/a
11	chr6:167763975-167764025	GM19239	blood:	n/a
12	chr6:167700000-167700050	HepG2	liver:	n/a
13	chr6:167761204-167761254	Jurkat	blood:	n/a
14	chr6:167764967-167765017	PrEC	prostate:	n/a
15	chr6:167753807-167753857	HRE	kidney:	n/a
16	chr6:167764967-167765017	A549	lung:	n/a
17	chr6:167704769-167704819	PFSK-1	brain:	n/a
18	chr6:167738425-167738475	NHBE	bronchial:	n/a
19	chr6:167737937-167737987	HRCEpiC	kidney:	n/a
20	chr6:167763975-167764025	HMEC	breast:	n/a
21	chr6:167705253-167705303	PFSK-1	brain:	n/a
22	chr6:167704808-167704858	PFSK-1	brain:	n/a
23	chr6:167764620-167764670	HepG2	liver:	n/a
24	chr6:167753807-167753857	H1-hESC	embryonic stem cell:	embryo
25	chr6:167705253-167705303	AG09309	skin:	n/a
26	chr6:167768382-167768432	Hepatocyte	liver:	n/a
27	chr6:167763819-167763869	PANC-1	pancreas:	n/a
28	chr6:167704808-167704858	ovcar-3	ovarian:	n/a
29	chr6:167704808-167704858	AoSMC	blood vessel:	n/a
30	chr6:167717196-167717246	IMR90	lung:	fetal
31	chr6:167738592-167738642	GM12892	blood:	n/a
32	chr6:167739618-167739668	GM12891	blood:	n/a
33	chr6:167704769-167704819	HRCEpiC	kidney:	n/a
34	chr6:167705253-167705303	BE2_C	brain:	n/a
35	chr6:167764967-167765017	SAEC	small airway:	n/a
36	chr6:167763320-167763370	GM12878	blood:	n/a
37	chr6:167763758-167763808	BE2_C	brain:	n/a
38	chr6:167709237-167709287	LNCaP	prostate:	n/a
39	chr6:167727700-167727750	AG04450	lung:	fetal
40	chr6:167753807-167753857	SKMC	muscle:	n/a
41	chr6:167734054-167734104	NT2-D1	testis:	n/a
42	chr6:167718461-167718511	NHBE	bronchial:	n/a
43	chr6:167704808-167704858	GM06990	blood:	n/a
44	chr6:167717196-167717246	HCPEpiC	choroid plexus:	n/a
45	chr6:167756099-167756149	Hela-S3	cervix:	n/a
46	chr6:167765215-167765265	T-47D	breast:	n/a
47	chr6:167703591-167703641	K562	blood:	n/a
48	chr6:167710360-167710410	HIPEpiC	eye:	n/a
49	chr6:167762783-167762833	H1-hESC	embryonic stem cell:	embryo
50	chr6:167738592-167738642	HIPEpiC	eye:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:167699179..167702166-chr6:167703091..167705361,2	K562	blood:
2	chr6:167631565..167632072-chr6:167702069..167702692,3	K562	blood:
3	chr6:167702039..167702568-chr6:167764606..167765474,2	MCF-7	breast:
4	chr6:167715327..167717333-chr6:167717541..167719931,2	MCF-7	breast:
5	chr6:167743283..167745523-chr6:167751106..167753120,2	K562	blood:
6	chr6:167744023..167747282-chr6:167750789..167753119,3	K562	blood:
7	chr6:167615262..167616947-chr6:167733556..167735117,2	MCF-7	breast:
8	chr6:167734899..167737753-chr6:167743376..167745822,2	MCF-7	breast:
9	chr6:167702039..167702568-chr6:167764606..167765474,2	MCF-7	breast:
10	chr6:167734899..167737753-chr6:167743376..167745822,2	MCF-7	breast:
11	chr6:167187967..167188932-chr6:167764453..167765086,2	K562	blood:
12	chr6:167703616..167705764-chr6:167717598..167719278,2	MCF-7	breast:
13	chr6:167736614..167738249-chr6:167740426..167742938,2	K562	blood:
14	chr6:167636874..167638495-chr6:167694115..167696567,2	K562	blood:
15	chr1:28836187..28837925-chr6:167694572..167696254,2	K562	blood:
16	chr6:167744023..167747282-chr6:167750789..167753119,3	K562	blood:
17	chr6:167743283..167745523-chr6:167751106..167753120,2	K562	blood:
18	chr6:167736614..167738249-chr6:167740426..167742938,2	K562	blood:
19	chr6:167715327..167717333-chr6:167717541..167719931,2	MCF-7	breast:
20	chr6:167631751..167632287-chr6:167701939..167702527,2	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UNC93A-2	chr6:167760960-167761541	NONHSAT116094
2	lnc-UNC93A-3	chr6:167764976-167765446	NONHSAT116095
3	lnc-UNC93A-3	chr6:167764293-167764966	NONHSAT116095

No data

Variant related genes	Relation type
UNC93A	TF binding region
TTLL2	TF binding region
ENSG00000217447	TF binding region
UNC93A	CpG island
TTLL2	CpG island
ENSG00000217447	CpG island
ENSG00000180198	chromatin interactions
ENSG00000112494	chromatin interactions

Extended variants
information (count: 4322 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:4322 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs139629668	chr6:167695214-167695215	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs192571622	chr6:167695247-167695248	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs184504171	chr6:167695250-167695251	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs144255891	chr6:167695269-167695270	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs146552996	chr6:167695277-167695278	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs549439424	chr6:167695290-167695291	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs533069728	chr6:167695299-167695300	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs188099403	chr6:167695305-167695306	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs80344568	chr6:167695327-167695328	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs60902278	chr6:167695339-167695340	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs529212185	chr6:167695382-167695383	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs550620724	chr6:167695388-167695389	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs551327435	chr6:167695439-167695440	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs376261745	chr6:167695465-167695466	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs73790155	chr6:167695501-167695502	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs565730561	chr6:167695528-167695529	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs182081999	chr6:167695535-167695536	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs566272492	chr6:167695547-167695548	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs533531192	chr6:167695578-167695579	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs184872864	chr6:167695613-167695614	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs77986267	chr6:167695614-167695615	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs189204024	chr6:167695631-167695632	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs567109207	chr6:167695654-167695655	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs578089008	chr6:167695700-167695701	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs545321986	chr6:167695722-167695723	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs56000381	chr6:167695773-167695774	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs572606923	chr6:167695777-167695778	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs543021319	chr6:167695799-167695800	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs561236183	chr6:167695820-167695821	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs531621746	chr6:167695825-167695826	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs181751355	chr6:167695831-167695832	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs562642050	chr6:167695838-167695839	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs533142765	chr6:167695840-167695841	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs139708024	chr6:167695850-167695851	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs56286801	chr6:167695863-167695864	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs527357585	chr6:167695864-167695865	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs186640953	chr6:167695881-167695882	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs149767987	chr6:167695935-167695936	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs55928844	chr6:167695944-167695945	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs537446995	chr6:167695945-167695946	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs73790156	chr6:167695947-167695948	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs571886934	chr6:167695952-167695953	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs539206674	chr6:167695998-167695999	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs73259188	chr6:167696079-167696080	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs73259191	chr6:167696173-167696174	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs73259192	chr6:167696217-167696218	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs555107934	chr6:167696231-167696232	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs446043	chr6:167696237-167696238	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs73790161	chr6:167696244-167696245	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs562787459	chr6:167696267-167696268	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:931 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:167689200-167702400	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr6:167690800-167698600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr6:167691200-167697600	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr6:167692400-167702400	Weak transcription	Thymus	Thymus
5	chr6:167693200-167695400	Enhancers	H9 Cell Line	embryonic stem cell
6	chr6:167693200-167696600	Enhancers	HepG2	liver
7	chr6:167693400-167696800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
8	chr6:167693400-167698800	Weak transcription	Fetal Brain Female	brain
9	chr6:167693600-167697200	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr6:167693800-167695600	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr6:167694000-167695400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr6:167694000-167695600	Enhancers	Stomach Mucosa	stomach
13	chr6:167694000-167696000	Enhancers	Fetal Intestine Large	intestine
14	chr6:167694200-167696000	Enhancers	Fetal Intestine Small	intestine
15	chr6:167694200-167697400	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr6:167694400-167696200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr6:167694600-167697200	Weak transcription	Fetal Brain Male	brain
18	chr6:167694800-167695400	Enhancers	Gastric	stomach
19	chr6:167695000-167696200	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr6:167695000-167696400	Weak transcription	HUES64 Cell Line	embryonic stem cell
21	chr6:167695200-167695400	Enhancers	H1 Cell Line	embryonic stem cell
22	chr6:167695200-167696400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr6:167695400-167696200	Weak transcription	H1 Cell Line	embryonic stem cell
24	chr6:167695400-167696200	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr6:167695400-167696200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr6:167695400-167698600	Weak transcription	Gastric	stomach
27	chr6:167695600-167696000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
28	chr6:167696000-167697200	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr6:167696000-167697600	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr6:167696000-167699600	Weak transcription	Fetal Intestine Small	intestine
31	chr6:167696200-167696400	Enhancers	Fetal Thymus	thymus
32	chr6:167696200-167696600	Enhancers	H9 Cell Line	embryonic stem cell
33	chr6:167696200-167697200	Enhancers	H1 Cell Line	embryonic stem cell
34	chr6:167696200-167697200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr6:167696200-167697400	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr6:167696200-167697600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr6:167696400-167697000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr6:167696400-167697000	Weak transcription	Fetal Thymus	thymus
39	chr6:167696400-167697400	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr6:167696600-167696800	Weak transcription	H9 Cell Line	embryonic stem cell
41	chr6:167696600-167697600	Weak transcription	HepG2	liver
42	chr6:167696800-167697600	Enhancers	H9 Cell Line	embryonic stem cell
43	chr6:167696800-167705800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
44	chr6:167697000-167697200	Enhancers	Fetal Thymus	thymus
45	chr6:167697000-167702400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr6:167697200-167697600	Enhancers	Fetal Brain Male	brain
47	chr6:167697200-167698600	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr6:167697200-167702000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
49	chr6:167697200-167702400	Weak transcription	Fetal Thymus	thymus
50	chr6:167697200-167705200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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