Variant report

Variant	nsv1035070
Chromosome Location	chr6:167696510-167785109
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1362)
CpG islands
(count:2503)
Chromatin interactive
region (count:19)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1362 , 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	chr6:167723215-167724601	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:167722138-167722657	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:167704338-167705733	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:167754780-167756165	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:167762709-167763005	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:167702230-167702578	HepG2	liver:	n/a	n/a
8	ATF1	chr6:167727339-167727444	K562	blood:	n/a	n/a
9	ATF1	chr6:167702337-167702425	K562	blood:	n/a	n/a
10	ATF2	chr6:167764810-167765270	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr6:167764830-167765266	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr6:167764960-167765154	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr6:167754224-167754403	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr6:167702257-167702472	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr6:167726056-167726329	GM12878	blood:	n/a	n/a
16	BATF	chr6:167764807-167765183	GM12878	blood:	n/a	n/a
17	BATF	chr6:167726053-167726251	GM12878	blood:	n/a	n/a
18	BATF	chr6:167765430-167765771	GM12878	blood:	n/a	n/a
19	BATF	chr6:167702166-167702414	GM12878	blood:	n/a	n/a
20	BATF	chr6:167765440-167765736	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	chr6:167733370-167733629	HepG2	liver:	n/a	n/a
24	BHLHE40	chr6:167723177-167724281	HepG2	liver:	n/a	n/a
25	BHLHE40	chr6:167764869-167765070	K562	blood:	n/a	n/a
26	BHLHE40	chr6:167723198-167723690	HepG2	liver:	n/a	n/a
27	BHLHE40	chr6:167755531-167755951	HepG2	liver:	n/a	n/a
28	BHLHE40	chr6:167702270-167702451	K562	blood:	n/a	n/a
29	BHLHE40	chr6:167764785-167765457	GM12878	blood:	n/a	n/a
30	BHLHE40	chr6:167732490-167732554	GM12878	blood:	n/a	n/a
31	BHLHE40	chr6:167704696-167705644	HepG2	liver:	n/a	n/a
32	BHLHE40	chr6:167702264-167702463	HepG2	liver:	n/a	n/a
33	BHLHE40	chr6:167754879-167756141	HepG2	liver:	n/a	n/a
34	BHLHE40	chr6:167755635-167755964	HepG2	liver:	n/a	n/a
35	BHLHE40	chr6:167722070-167722725	HepG2	liver:	n/a	chr6:167722523-167722539
36	BHLHE40	chr6:167733252-167733970	HepG2	liver:	n/a	n/a
37	BHLHE40	chr6:167722146-167722527	HepG2	liver:	n/a	n/a
38	BHLHE40	chr6:167699851-167700081	HepG2	liver:	n/a	n/a
39	BRCA1	chr6:167764922-167765205	H1-hESC	embryonic stem cell:	n/a	n/a
40	BRCA1	chr6:167750805-167750846	HepG2	liver:	n/a	n/a
41	BRCA1	chr6:167722055-167722521	HepG2	liver:	n/a	n/a
42	CBX3	chr6:167708762-167709384	K562	blood:	n/a	n/a
43	CBX3	chr6:167702109-167702642	K562	blood:	n/a	n/a
44	CBX3	chr6:167708857-167709379	K562	blood:	n/a	n/a
45	CEBPB	chr6:167742236-167742292	K562	blood:	n/a	n/a
46	CEBPB	chr6:167722086-167722440	HepG2	liver:	n/a	n/a
47	CEBPB	chr6:167705083-167705467	HepG2	liver:	n/a	chr6:167705263-167705276 chr6:167705265-167705274 chr6:167705263-167705274
48	CEBPB	chr6:167723167-167723598	HepG2	liver:	n/a	n/a
49	CEBPB	chr6:167705111-167705421	IMR90	lung:	n/a	chr6:167705263-167705276 chr6:167705265-167705274 chr6:167705263-167705274
50	CEBPB	chr6:167705074-167705472	HepG2	liver:	n/a	chr6:167705263-167705276 chr6:167705265-167705274 chr6:167705263-167705274

(count:2503 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:167708827-167708877	GM12878	blood:	n/a
2	chr6:167764967-167765017	IMR90	lung:	fetal
3	chr6:167708827-167708877	GM12878	blood:	n/a
4	chr6:167764967-167765017	IMR90	lung:	fetal
5	chr6:167734054-167734104	HRCEpiC	kidney:	n/a
6	chr6:167709720-167709770	SK-N-MC	brain:	n/a
7	chr6:167756099-167756149	SK-N-SH	brain:	n/a
8	chr6:167763320-167763370	PFSK-1	brain:	n/a
9	chr6:167738342-167738392	IMR90	lung:	fetal
10	chr6:167764146-167764196	GM12892	blood:	n/a
11	chr6:167704188-167704238	HCT-116	colon:	n/a
12	chr6:167734054-167734104	U87	brain:	n/a
13	chr6:167700000-167700050	AG09319	gingival:	n/a
14	chr6:167709720-167709770	PANC-1	pancreas:	n/a
15	chr6:167738342-167738392	PANC-1	pancreas:	n/a
16	chr6:167764620-167764670	HCM	heart:	n/a
17	chr6:167709237-167709287	NH-A	brain:	n/a
18	chr6:167704188-167704238	PANC-1	pancreas:	n/a
19	chr6:167705253-167705303	HRE	kidney:	n/a
20	chr6:167738277-167738327	Hela-S3	cervix:	n/a
21	chr6:167770239-167770289	SK-N-SH	brain:	n/a
22	chr6:167704769-167704819	NB4	blood:	n/a
23	chr6:167709237-167709287	HCF	heart:	n/a
24	chr6:167708827-167708877	SK-N-SH_RA	brain:	n/a
25	chr6:167763975-167764025	HPAEpiC	pulmonary alveolar:	n/a
26	chr6:167708827-167708877	AG04449	skin:	fetal
27	chr6:167739618-167739668	NT2-D1	testis:	n/a
28	chr6:167704673-167704723	AG10803	skin:	n/a
29	chr6:167703894-167703944	HepG2	liver:	n/a
30	chr6:167738594-167738644	Jurkat	blood:	n/a
31	chr6:167710360-167710410	HCM	heart:	n/a
32	chr6:167764967-167765017	SK-N-MC	brain:	n/a
33	chr6:167763819-167763869	NHBE	bronchial:	n/a
34	chr6:167703894-167703944	HCPEpiC	choroid plexus:	n/a
35	chr6:167738342-167738392	PrEC	prostate:	n/a
36	chr6:167718461-167718511	HIPEpiC	eye:	n/a
37	chr6:167734054-167734104	HIPEpiC	eye:	n/a
38	chr6:167765110-167765160	BE2_C	brain:	n/a
39	chr6:167764967-167765017	U87	brain:	n/a
40	chr6:167768382-167768432	NH-A	brain:	n/a
41	chr6:167705253-167705303	RPTEC	kidney:	n/a
42	chr6:167704673-167704723	HUVEC	blood vessel:	n/a
43	chr6:167709720-167709770	SK-N-SH_RA	brain:	n/a
44	chr6:167763320-167763370	Jurkat	blood:	n/a
45	chr6:167700000-167700050	H1-hESC	embryonic stem cell:	embryo
46	chr6:167761204-167761254	LNCaP	prostate:	n/a
47	chr6:167765110-167765160	PFSK-1	brain:	n/a
48	chr6:167717313-167717363	HEEpiC	esophagus:	n/a
49	chr6:167763819-167763869	GM12892	blood:	n/a
50	chr6:167717313-167717363	K562	blood:	n/a

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

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

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UNC93A-3	chr6:167764976-167765446	NONHSAT116095
2	lnc-UNC93A-2	chr6:167760960-167761541	NONHSAT116094
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
ENSG00000112494	chromatin interactions

Extended variants
information (count: 4259 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:4259 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1209349	chr6:167696510-167696511	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs536840060	chr6:167696546-167696547	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs373964298	chr6:167696624-167696625	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs555041744	chr6:167696627-167696628	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs575539136	chr6:167696628-167696629	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs576496824	chr6:167696663-167696664	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs56353955	chr6:167696664-167696665	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs558654381	chr6:167696681-167696682	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs56073794	chr6:167696689-167696690	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs1079499	chr6:167696715-167696716	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs560019820	chr6:167696726-167696727	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs59227187	chr6:167696755-167696756	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs542452916	chr6:167696770-167696771	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs561020716	chr6:167696792-167696793	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs191484026	chr6:167696808-167696809	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs531331764	chr6:167696862-167696863	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs55752300	chr6:167696867-167696868	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs377018675	chr6:167696888-167696889	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs76913197	chr6:167696891-167696892	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs532153503	chr6:167696899-167696900	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs3010558	chr6:167696948-167696949	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs181131444	chr6:167696962-167696963	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs185100872	chr6:167696976-167696977	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs6935358	chr6:167696981-167696982	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs537115677	chr6:167696982-167696983	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs201595365	chr6:167696984-167696985	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs372570095	chr6:167696990-167696991	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs576781660	chr6:167696998-167696999	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs183432107	chr6:167697009-167697010	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs6935543	chr6:167697092-167697093	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs187710073	chr6:167697128-167697129	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs77082908	chr6:167697151-167697152	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs6934251	chr6:167697155-167697156	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs191863584	chr6:167697175-167697176	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs1212940	chr6:167697179-167697180	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs543110477	chr6:167697247-167697248	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs6914818	chr6:167697254-167697255	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs183725225	chr6:167697269-167697270	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs547455654	chr6:167697342-167697343	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs377311847	chr6:167697384-167697385	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs6934766	chr6:167697390-167697391	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs373165045	chr6:167697392-167697393	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs56058730	chr6:167697414-167697415	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs386708583	chr6:167697425-167697426	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs206988	chr6:167697426-167697427	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs552389850	chr6:167697438-167697439	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs570653698	chr6:167697464-167697465	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs188202408	chr6:167697470-167697471	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs6936514	chr6:167697621-167697622	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs77389693	chr6:167697625-167697626	Weak transcription Enhancers	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:914 , 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	chr6:167693200-167696600	Enhancers	HepG2	liver
6	chr6:167693400-167696800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
7	chr6:167693400-167698800	Weak transcription	Fetal Brain Female	brain
8	chr6:167693600-167697200	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr6:167694200-167697400	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr6:167694600-167697200	Weak transcription	Fetal Brain Male	brain
11	chr6:167695400-167698600	Weak transcription	Gastric	stomach
12	chr6:167696000-167697200	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr6:167696000-167697600	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr6:167696000-167699600	Weak transcription	Fetal Intestine Small	intestine
15	chr6:167696200-167696600	Enhancers	H9 Cell Line	embryonic stem cell
16	chr6:167696200-167697200	Enhancers	H1 Cell Line	embryonic stem cell
17	chr6:167696200-167697200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr6:167696200-167697400	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr6:167696200-167697600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr6:167696400-167697000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr6:167696400-167697000	Weak transcription	Fetal Thymus	thymus
22	chr6:167696400-167697400	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr6:167696600-167696800	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr6:167696600-167697600	Weak transcription	HepG2	liver
25	chr6:167696800-167697600	Enhancers	H9 Cell Line	embryonic stem cell
26	chr6:167696800-167705800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
27	chr6:167697000-167697200	Enhancers	Fetal Thymus	thymus
28	chr6:167697000-167702400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr6:167697200-167697600	Enhancers	Fetal Brain Male	brain
30	chr6:167697200-167698600	Weak transcription	H1 Cell Line	embryonic stem cell
31	chr6:167697200-167702000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
32	chr6:167697200-167702400	Weak transcription	Fetal Thymus	thymus
33	chr6:167697200-167705200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr6:167697400-167702000	Weak transcription	HUES64 Cell Line	embryonic stem cell
35	chr6:167697400-167702400	Weak transcription	HUES6 Cell Line	embryonic stem cell
36	chr6:167697600-167699600	Enhancers	HepG2	liver
37	chr6:167697600-167700800	Weak transcription	Fetal Brain Male	brain
38	chr6:167697600-167702400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr6:167697600-167706200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr6:167698600-167699000	Enhancers	H1 Cell Line	embryonic stem cell
41	chr6:167698600-167699000	Enhancers	Gastric	stomach
42	chr6:167698600-167699000	Enhancers	Rectal Mucosa Donor 31	rectum
43	chr6:167698600-167699200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr6:167698600-167699200	Enhancers	Fetal Muscle Leg	muscle
45	chr6:167698600-167699200	Enhancers	Pancreas	Pancrea
46	chr6:167698800-167699000	Flanking Active TSS	Liver	Liver
47	chr6:167698800-167699200	Enhancers	Fetal Brain Female	brain
48	chr6:167698800-167699200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
49	chr6:167699000-167699200	Active TSS	Liver	Liver
50	chr6:167699000-167702400	Weak transcription	H1 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links