Variant report

Variant	nsv1022342
Chromosome Location	chr6:167736870-167781194
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:525)
CpG islands
(count:1404)
Chromatin interactive
region (count:10)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:525 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:167762709-167763005	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:167754780-167756165	HepG2	liver:	n/a	n/a
3	ATF2	chr6:167764810-167765270	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr6:167764830-167765266	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr6:167764960-167765154	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr6:167754224-167754403	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr6:167765430-167765771	GM12878	blood:	n/a	n/a
8	BATF	chr6:167764807-167765183	GM12878	blood:	n/a	n/a
9	BATF	chr6:167765440-167765736	GM12878	blood:	n/a	n/a
10	BCLAF1	chr6:167764829-167765189	GM12878	blood:	n/a	chr6:167764879-167764888 chr6:167765036-167765044
11	BHLHE40	chr6:167755531-167755951	HepG2	liver:	n/a	n/a
12	BHLHE40	chr6:167764785-167765457	GM12878	blood:	n/a	n/a
13	BHLHE40	chr6:167764869-167765070	K562	blood:	n/a	n/a
14	BHLHE40	chr6:167754879-167756141	HepG2	liver:	n/a	n/a
15	BHLHE40	chr6:167755635-167755964	HepG2	liver:	n/a	n/a
16	BRCA1	chr6:167764922-167765205	H1-hESC	embryonic stem cell:	n/a	n/a
17	BRCA1	chr6:167750805-167750846	HepG2	liver:	n/a	n/a
18	CEBPB	chr6:167764886-167765190	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr6:167742236-167742292	K562	blood:	n/a	n/a
20	CEBPB	chr6:167779877-167780146	Hela-S3	cervix:	n/a	chr6:167780030-167780041 chr6:167780010-167780021
21	CEBPB	chr6:167762531-167762769	A549	lung:	n/a	n/a
22	CEBPB	chr6:167755617-167756086	HepG2	liver:	n/a	n/a
23	CEBPB	chr6:167762489-167763000	HepG2	liver:	n/a	n/a
24	CEBPB	chr6:167742112-167742401	HepG2	liver:	n/a	n/a
25	CEBPB	chr6:167778443-167778483	K562	blood:	n/a	n/a
26	CEBPB	chr6:167779869-167780097	HepG2	liver:	n/a	chr6:167780030-167780041 chr6:167780010-167780021
27	CEBPB	chr6:167755544-167755995	HepG2	liver:	n/a	n/a
28	CEBPD	chr6:167755623-167755941	HepG2	liver:	n/a	n/a
29	CEBPZ	chr6:167755646-167756073	HepG2	liver:	n/a	n/a
30	CHD1	chr6:167765061-167765260	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr6:167764623-167765220	H1-hESC	embryonic stem cell:	n/a	chr6:167764680-167764690
32	CHD2	chr6:167755626-167755922	HepG2	liver:	n/a	n/a
33	CREB1	chr6:167762651-167763058	HepG2	liver:	n/a	n/a
34	CREB1	chr6:167755519-167756217	HepG2	liver:	n/a	n/a
35	CREB1	chr6:167755173-167756203	HepG2	liver:	n/a	n/a
36	CREB1	chr6:167764773-167765270	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr6:167764966-167765116	HepG2	liver:	n/a	chr6:167765037-167765055 chr6:167765039-167765052
38	CTCF	chr6:167764940-167765090	GM12873	blood:	n/a	chr6:167765037-167765055 chr6:167765039-167765052
39	CTCF	chr6:167764980-167765130	GM12871	blood:	n/a	chr6:167765037-167765055 chr6:167765039-167765052
40	CTCF	chr6:167764936-167765186	LNCaP	prostate:	n/a	chr6:167765037-167765055 chr6:167765039-167765052
41	CTCF	chr6:167764980-167765130	GM12873	blood:	n/a	chr6:167765037-167765055 chr6:167765039-167765052
42	CTCF	chr6:167765020-167765170	HL-60	blood:	n/a	chr6:167765037-167765055 chr6:167765039-167765052
43	CTCF	chr6:167764853-167765253	K562	blood:	n/a	chr6:167765037-167765055 chr6:167765039-167765052
44	CTCF	chr6:167742614-167742694	GM13977	blood:	n/a	n/a
45	CTCF	chr6:167764940-167765090	GM12864	blood:	n/a	chr6:167765037-167765055 chr6:167765039-167765052
46	CTCF	chr6:167778687-167778735	HepG2	liver:	n/a	n/a
47	CTCF	chr6:167764960-167765110	Caco-2	colon:	n/a	chr6:167765037-167765055 chr6:167765039-167765052
48	CTCF	chr6:167764980-167765130	GM12864	blood:	n/a	chr6:167765037-167765055 chr6:167765039-167765052
49	CTCF	chr6:167775539-167775568	LNCaP	prostate:	n/a	n/a
50	CTCF	chr6:167764550-167764595	Fibrobl	skin:	n/a	n/a

(count:1404 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:167753807-167753857	AG10803	skin:	n/a
2	chr6:167753807-167753857	AG10803	skin:	n/a
3	chr6:167764967-167765017	NB4	blood:	n/a
4	chr6:167764146-167764196	HMEC	breast:	n/a
5	chr6:167770239-167770289	HCM	heart:	n/a
6	chr6:167762783-167762833	GM12891	blood:	n/a
7	chr6:167763320-167763370	SK-N-SH	brain:	n/a
8	chr6:167756099-167756149	HCT-116	colon:	n/a
9	chr6:167764620-167764670	GM19239	blood:	n/a
10	chr6:167765110-167765160	SK-N-SH_RA	brain:	n/a
11	chr6:167770239-167770289	ECC-1	luminal epithelium:	n/a
12	chr6:167765110-167765160	Jurkat	blood:	n/a
13	chr6:167762783-167762833	Hela-S3	cervix:	n/a
14	chr6:167765110-167765160	HCPEpiC	choroid plexus:	n/a
15	chr6:167756099-167756149	PANC-1	pancreas:	n/a
16	chr6:167770239-167770289	NHDF-neo	bronchial:	n/a
17	chr6:167764523-167764573	ProgFib	skin:	n/a
18	chr6:167770239-167770289	AG09309	skin:	n/a
19	chr6:167761204-167761254	HCF	heart:	n/a
20	chr6:167765110-167765160	HEEpiC	esophagus:	n/a
21	chr6:167761204-167761254	HIPEpiC	eye:	n/a
22	chr6:167763320-167763370	HIPEpiC	eye:	n/a
23	chr6:167764146-167764196	GM12891	blood:	n/a
24	chr6:167756099-167756149	NH-A	brain:	n/a
25	chr6:167764620-167764670	AoSMC	blood vessel:	n/a
26	chr6:167737937-167737987	HRCEpiC	kidney:	n/a
27	chr6:167763758-167763808	U87	brain:	n/a
28	chr6:167738594-167738644	HCF	heart:	n/a
29	chr6:167764523-167764573	SK-N-SH_RA	brain:	n/a
30	chr6:167762783-167762833	SKMC	muscle:	n/a
31	chr6:167738594-167738644	Hela-S3	cervix:	n/a
32	chr6:167763975-167764025	Caco-2	colon:	n/a
33	chr6:167763819-167763869	Caco-2	colon:	n/a
34	chr6:167738594-167738644	HEK293	kidney:	embryo
35	chr6:167770239-167770289	SK-N-SH	brain:	n/a
36	chr6:167764146-167764196	AG04449	skin:	fetal
37	chr6:167764967-167765017	AG10803	skin:	n/a
38	chr6:167738592-167738642	HEK293	kidney:	embryo
39	chr6:167764146-167764196	AG04450	lung:	fetal
40	chr6:167753807-167753857	PANC-1	pancreas:	n/a
41	chr6:167738342-167738392	SK-N-SH_RA	brain:	n/a
42	chr6:167762783-167762833	AoSMC	blood vessel:	n/a
43	chr6:167738277-167738327	NHBE	bronchial:	n/a
44	chr6:167764146-167764196	Hepatocyte	liver:	n/a
45	chr6:167763758-167763808	Caco-2	colon:	n/a
46	chr6:167762783-167762833	HPAEpiC	pulmonary alveolar:	n/a
47	chr6:167763758-167763808	MCF10A-Er-Src	breast:	n/a
48	chr6:167763819-167763869	HCM	heart:	n/a
49	chr6:167763975-167764025	NHDF-neo	bronchial:	n/a
50	chr6:167738592-167738642	HCF	heart:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr6:167187967..167188932-chr6:167764453..167765086,2	K562	blood:
2	chr6:167702039..167702568-chr6:167764606..167765474,2	MCF-7	breast:
3	chr6:167736614..167738249-chr6:167740426..167742938,2	K562	blood:
4	chr6:167744023..167747282-chr6:167750789..167753119,3	K562	blood:
5	chr6:167743283..167745523-chr6:167751106..167753120,2	K562	blood:
6	chr6:167744023..167747282-chr6:167750789..167753119,3	K562	blood:
7	chr6:167736614..167738249-chr6:167740426..167742938,2	K562	blood:
8	chr6:167734899..167737753-chr6:167743376..167745822,2	MCF-7	breast:
9	chr6:167743283..167745523-chr6:167751106..167753120,2	K562	blood:
10	chr6:167734899..167737753-chr6:167743376..167745822,2	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
TTLL2	TF binding region
ENSG00000217447	TF binding region
TTLL2	CpG island
ENSG00000217447	CpG island

Extended variants
information (count: 1809 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:1809 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3814085	chr6:167736870-167736871	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs528158789	chr6:167736889-167736890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs3814084	chr6:167736952-167736953	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs568083378	chr6:167736953-167736954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs147600890	chr6:167737034-167737035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs7754781	chr6:167737067-167737068	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs192861445	chr6:167737090-167737091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs7754798	chr6:167737097-167737098	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs7754679	chr6:167737117-167737118	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs7755105	chr6:167737127-167737128	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs7754688	chr6:167737138-167737139	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs35806393	chr6:167737180-167737181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs555782114	chr6:167737197-167737198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs7754988	chr6:167737199-167737200	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs7755252	chr6:167737206-167737207	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs12110628	chr6:167737212-167737213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs142052762	chr6:167737276-167737277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs545725634	chr6:167737284-167737285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs143045346	chr6:167737359-167737360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs564053594	chr6:167737369-167737370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs528261301	chr6:167737442-167737443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs3814083	chr6:167737450-167737451	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs3814082	chr6:167737451-167737452	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs35358774	chr6:167737465-167737466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs35448006	chr6:167737496-167737497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs185176616	chr6:167737561-167737562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs7755956	chr6:167737648-167737649	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs3814081	chr6:167737675-167737676	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs148187550	chr6:167737676-167737677	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs567897716	chr6:167737681-167737682	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs3814080	chr6:167737682-167737683	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs12525594	chr6:167737695-167737696	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs534359979	chr6:167737722-167737723	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs115147243	chr6:167737755-167737756	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs140062791	chr6:167737763-167737764	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs544404264	chr6:167737764-167737765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs150486584	chr6:167737780-167737781	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs577581244	chr6:167737791-167737792	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs545021058	chr6:167737836-167737837	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs578063629	chr6:167737851-167737852	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs563992083	chr6:167737852-167737853	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs188613690	chr6:167737891-167737892	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs73266911	chr6:167737957-167737958	Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs115672441	chr6:167737974-167737975	Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
45	rs114987520	chr6:167737975-167737976	Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
46	rs71004122	chr6:167737981-167737982	Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
47	rs398003330	chr6:167738001-167738002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs550664634	chr6:167738005-167738006	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs572723065	chr6:167738035-167738036	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs562594316	chr6:167738040-167738041	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:498 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:167731200-167738400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:167731200-167738400	Weak transcription	Fetal Brain Female	brain
3	chr6:167732400-167737600	Weak transcription	Fetal Brain Male	brain
4	chr6:167733000-167737800	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr6:167734400-167739400	Weak transcription	Fetal Intestine Small	intestine
6	chr6:167735200-167739200	Weak transcription	HepG2	liver
7	chr6:167737400-167737800	Enhancers	Stomach Mucosa	stomach
8	chr6:167737600-167739800	Enhancers	Fetal Brain Male	brain
9	chr6:167737800-167739000	Enhancers	Placenta Amnion	Placenta Amnion
10	chr6:167738200-167738400	Weak transcription	Pancreas	Pancrea
11	chr6:167738400-167738600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr6:167738400-167742200	Enhancers	Fetal Brain Female	brain
13	chr6:167738600-167738800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr6:167738600-167738800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr6:167738600-167738800	Enhancers	Spleen	Spleen
16	chr6:167738800-167739000	Weak transcription	Pancreas	Pancrea
17	chr6:167738800-167744200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr6:167739200-167739600	Enhancers	HepG2	liver
19	chr6:167739400-167739800	Enhancers	Fetal Intestine Small	intestine
20	chr6:167739600-167741400	Weak transcription	HepG2	liver
21	chr6:167739800-167740200	Weak transcription	Fetal Brain Male	brain
22	chr6:167739800-167745200	Weak transcription	Fetal Intestine Small	intestine
23	chr6:167740200-167742800	Enhancers	Fetal Brain Male	brain
24	chr6:167740800-167742400	Enhancers	Ovary	ovary
25	chr6:167741400-167742800	Enhancers	HepG2	liver
26	chr6:167741600-167742400	Enhancers	Thymus	Thymus
27	chr6:167742200-167742600	Weak transcription	Fetal Brain Female	brain
28	chr6:167742400-167743800	Weak transcription	Ovary	ovary
29	chr6:167742600-167743200	Enhancers	Fetal Brain Female	brain
30	chr6:167742600-167750400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr6:167742800-167744200	Weak transcription	HepG2	liver
32	chr6:167742800-167751400	Weak transcription	Fetal Brain Male	brain
33	chr6:167743800-167744400	Enhancers	Ovary	ovary
34	chr6:167744000-167744200	Weak transcription	Spleen	Spleen
35	chr6:167744200-167744400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
36	chr6:167744200-167744600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr6:167744200-167744600	Enhancers	Lung	lung
38	chr6:167744200-167745400	Enhancers	Spleen	Spleen
39	chr6:167744200-167745800	Enhancers	HepG2	liver
40	chr6:167744400-167745600	Enhancers	Stomach Mucosa	stomach
41	chr6:167744600-167750000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr6:167745200-167745800	Enhancers	Fetal Intestine Small	intestine
43	chr6:167745400-167746000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr6:167745400-167750000	Weak transcription	Spleen	Spleen
45	chr6:167745600-167745800	Flanking Active TSS	Duodenum Mucosa	Duodenum
46	chr6:167745600-167745800	Enhancers	Pancreas	Pancrea
47	chr6:167745800-167750000	Weak transcription	HepG2	liver
48	chr6:167745800-167753600	Weak transcription	Pancreas	Pancrea
49	chr6:167749600-167749800	Enhancers	Fetal Thymus	thymus
50	chr6:167749600-167752400	Enhancers	Thymus	Thymus

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