Variant report

Variant	nsv1031591
Chromosome Location	chr6:167739556-167832936
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1018)
CpG islands
(count:2995)
Chromatin interactive
region (count:16)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1018 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

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	chr6:167809998-167810531	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:167811767-167812223	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:167754780-167756165	HepG2	liver:	n/a	n/a
5	ATF2	chr6:167764810-167765270	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr6:167764830-167765266	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr6:167754224-167754403	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr6:167764960-167765154	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr6:167785311-167785621	GM12878	blood:	n/a	n/a
10	BATF	chr6:167801477-167801674	GM12878	blood:	n/a	n/a
11	BATF	chr6:167765440-167765736	GM12878	blood:	n/a	n/a
12	BATF	chr6:167764807-167765183	GM12878	blood:	n/a	n/a
13	BATF	chr6:167765430-167765771	GM12878	blood:	n/a	n/a
14	BCL11A	chr6:167799353-167799569	GM12878	blood:	n/a	n/a
15	BCL11A	chr6:167801917-167802109	GM12878	blood:	n/a	n/a
16	BCL11A	chr6:167801472-167801775	GM12878	blood:	n/a	n/a
17	BCL11A	chr6:167801474-167801790	GM12878	blood:	n/a	n/a
18	BCL11A	chr6:167800632-167800815	GM12878	blood:	n/a	n/a
19	BCLAF1	chr6:167764829-167765189	GM12878	blood:	n/a	chr6:167764879-167764888 chr6:167765036-167765044
20	BHLHE40	chr6:167764785-167765457	GM12878	blood:	n/a	n/a
21	BHLHE40	chr6:167811642-167812135	HepG2	liver:	n/a	n/a
22	BHLHE40	chr6:167755531-167755951	HepG2	liver:	n/a	n/a
23	BHLHE40	chr6:167811648-167812302	HepG2	liver:	n/a	n/a
24	BHLHE40	chr6:167826030-167826420	HepG2	liver:	n/a	n/a
25	BHLHE40	chr6:167814832-167815507	HepG2	liver:	n/a	chr6:167815146-167815155 chr6:167815144-167815157 chr6:167815147-167815156 chr6:167815140-167815161 chr6:167815146-167815155
26	BHLHE40	chr6:167754879-167756141	HepG2	liver:	n/a	n/a
27	BHLHE40	chr6:167764869-167765070	K562	blood:	n/a	n/a
28	BHLHE40	chr6:167810045-167810579	HepG2	liver:	n/a	n/a
29	BHLHE40	chr6:167755635-167755964	HepG2	liver:	n/a	n/a
30	BHLHE40	chr6:167815066-167815240	K562	blood:	n/a	chr6:167815146-167815155 chr6:167815144-167815157 chr6:167815147-167815156 chr6:167815140-167815161 chr6:167815146-167815155
31	BHLHE40	chr6:167827209-167827450	K562	blood:	n/a	n/a
32	BHLHE40	chr6:167785339-167785655	HepG2	liver:	n/a	n/a
33	BRCA1	chr6:167750805-167750846	HepG2	liver:	n/a	n/a
34	BRCA1	chr6:167811846-167812095	HepG2	liver:	n/a	n/a
35	BRCA1	chr6:167764922-167765205	H1-hESC	embryonic stem cell:	n/a	n/a
36	CBX3	chr6:167800537-167800803	K562	blood:	n/a	n/a
37	CEBPB	chr6:167778443-167778483	K562	blood:	n/a	n/a
38	CEBPB	chr6:167762531-167762769	A549	lung:	n/a	n/a
39	CEBPB	chr6:167810129-167810428	HepG2	liver:	n/a	n/a
40	CEBPB	chr6:167762489-167763000	HepG2	liver:	n/a	n/a
41	CEBPB	chr6:167779869-167780097	HepG2	liver:	n/a	chr6:167780030-167780041 chr6:167780010-167780021
42	CEBPB	chr6:167811663-167812136	HepG2	liver:	n/a	n/a
43	CEBPB	chr6:167742236-167742292	K562	blood:	n/a	n/a
44	CEBPB	chr6:167823739-167824431	HepG2	liver:	n/a	chr6:167824329-167824338 chr6:167824327-167824340
45	CEBPB	chr6:167755544-167755995	HepG2	liver:	n/a	n/a
46	CEBPB	chr6:167764886-167765190	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr6:167811682-167811930	HepG2	liver:	n/a	n/a
48	CEBPB	chr6:167742112-167742401	HepG2	liver:	n/a	n/a
49	CEBPB	chr6:167755617-167756086	HepG2	liver:	n/a	n/a
50	CEBPB	chr6:167779877-167780146	Hela-S3	cervix:	n/a	chr6:167780030-167780041 chr6:167780010-167780021

(count:2995 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:167786642-167786692	LNCaP	prostate:	n/a
2	chr6:167786592-167786642	GM12892	blood:	n/a
3	chr6:167803413-167803463	NH-A	brain:	n/a
4	chr6:167763819-167763869	ovcar-3	ovarian:	n/a
5	chr6:167810043-167810093	GM19239	blood:	n/a
6	chr6:167791153-167791203	GM06990	blood:	n/a
7	chr6:167786642-167786692	LNCaP	prostate:	n/a
8	chr6:167786592-167786642	GM12892	blood:	n/a
9	chr6:167803413-167803463	NH-A	brain:	n/a
10	chr6:167763819-167763869	ovcar-3	ovarian:	n/a
11	chr6:167810043-167810093	GM19239	blood:	n/a
12	chr6:167791153-167791203	GM06990	blood:	n/a
13	chr6:167794506-167794556	HNPCEpiC	eye:	n/a
14	chr6:167764620-167764670	CMK	blood:	n/a
15	chr6:167792741-167792791	AG09319	gingival:	n/a
16	chr6:167786059-167786109	ECC-1	luminal epithelium:	n/a
17	chr6:167789195-167789245	HIPEpiC	eye:	n/a
18	chr6:167791153-167791203	ProgFib	skin:	n/a
19	chr6:167763758-167763808	SK-N-SH	brain:	n/a
20	chr6:167814314-167814364	NHDF-neo	bronchial:	n/a
21	chr6:167786059-167786109	HRPEpiC	eye:	n/a
22	chr6:167770239-167770289	PFSK-1	brain:	n/a
23	chr6:167810343-167810393	CMK	blood:	n/a
24	chr6:167763975-167764025	AoSMC	blood vessel:	n/a
25	chr6:167739618-167739668	NB4	blood:	n/a
26	chr6:167797877-167797927	H1-hESC	embryonic stem cell:	embryo
27	chr6:167764967-167765017	HAEpiC	amniotic membrane:	n/a
28	chr6:167797877-167797927	HCM	heart:	n/a
29	chr6:167808366-167808416	HRCEpiC	kidney:	n/a
30	chr6:167810343-167810393	HRE	kidney:	n/a
31	chr6:167810343-167810393	BE2_C	brain:	n/a
32	chr6:167756099-167756149	AG09309	skin:	n/a
33	chr6:167809972-167810022	IMR90	lung:	fetal
34	chr6:167794374-167794424	HRCEpiC	kidney:	n/a
35	chr6:167809876-167809926	GM12891	blood:	n/a
36	chr6:167814257-167814307	HRPEpiC	eye:	n/a
37	chr6:167808551-167808601	ProgFib	skin:	n/a
38	chr6:167794506-167794556	HepG2	liver:	n/a
39	chr6:167791024-167791074	Hela-S3	cervix:	n/a
40	chr6:167756099-167756149	AG09319	gingival:	n/a
41	chr6:167794506-167794556	GM06990	blood:	n/a
42	chr6:167832664-167832714	GM12892	blood:	n/a
43	chr6:167786059-167786109	NT2-D1	testis:	n/a
44	chr6:167768382-167768432	MCF10A-Er-Src	breast:	n/a
45	chr6:167739618-167739668	BE2_C	brain:	n/a
46	chr6:167792741-167792791	GM19239	blood:	n/a
47	chr6:167764523-167764573	NB4	blood:	n/a
48	chr6:167809825-167809875	HMEC	breast:	n/a
49	chr6:167762783-167762833	HEK293	kidney:	embryo
50	chr6:167814257-167814307	Hela-S3	cervix:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr6:167736614..167738249-chr6:167740426..167742938,2	K562	blood:
2	chr6:167744023..167747282-chr6:167750789..167753119,3	K562	blood:
3	chr6:167823826..167826272-chr6:167829672..167831832,2	K562	blood:
4	chr6:167743283..167745523-chr6:167751106..167753120,2	K562	blood:
5	chr6:167818746..167821496-chr6:167831177..167833070,2	K562	blood:
6	chr6:167744023..167747282-chr6:167750789..167753119,3	K562	blood:
7	chr6:167813417..167815135-chr6:167817698..167819518,2	K562	blood:
8	chr20:57615578..57617834-chr6:167831422..167833295,2	MCF-7	breast:
9	chr6:167734899..167737753-chr6:167743376..167745822,2	MCF-7	breast:
10	chr6:167662732..167663315-chr6:167819023..167819880,2	K562	blood:
11	chr6:167743283..167745523-chr6:167751106..167753120,2	K562	blood:
12	chr6:167823826..167826272-chr6:167829672..167831832,2	K562	blood:
13	chr6:167187967..167188932-chr6:167764453..167765086,2	K562	blood:
14	chr6:167813417..167815135-chr6:167817698..167819518,2	K562	blood:
15	chr6:167702039..167702568-chr6:167764606..167765474,2	MCF-7	breast:
16	chr6:167818746..167821496-chr6:167831177..167833070,2	K562	blood:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TTLL2-1	chr6:167804760-167804979	XLOC_005541
2	lnc-TCP10-2	chr6:167810373-167814438	ucscGeneNc_uc003qvx_1
3	lnc-TCP10-2	chr6:167822441-167822752	ucscGeneNc_uc003qvx_1
4	lnc-TCP10-2	chr6:167821589-167821728	ucscGeneNc_uc003qvx_1
5	lnc-UNC93A-3	chr6:167764976-167765446	NONHSAT116095
6	lnc-UNC93A-2	chr6:167760960-167761541	NONHSAT116094
7	lnc-TCP10-3	chr6:167825862-167825976	ucscGeneNc_uc003qvy_1
8	lnc-TCP10-1	chr6:167787839-167789289	NONHSAT116097
9	lnc-TCP10-3	chr6:167823155-167825466	ucscGeneNc_uc003qvy_1
10	lnc-UNC93A-3	chr6:167764293-167764966	NONHSAT116095
11	lnc-TCP10-3	chr6:167826637-167827774	ucscGeneNc_uc003qvy_1
12	lnc-TTLL2-1	chr6:167803650-167803969	XLOC_005541
13	lnc-TCP10-1	chr6:167786578-167786848	NONHSAT116097

No data

Variant related genes	Relation type
TCP10	TF binding region
ENSG00000217447	TF binding region
TCP10	CpG island
ENSG00000217447	CpG island
ENSG00000101166	chromatin interactions

Extended variants
information (count: 3889 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:3889 , 50 per page) page: 1 2 3 4 5 6 7 ... 78

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73266925	chr6:167739589-167739590	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs77758019	chr6:167739595-167739596	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs9355235	chr6:167739653-167739654	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs145267000	chr6:167739654-167739655	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs370234987	chr6:167739663-167739664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs61630556	chr6:167739677-167739678	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs377155987	chr6:167739694-167739695	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs568165417	chr6:167739712-167739713	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs113553344	chr6:167739747-167739748	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs9456267	chr6:167739769-167739770	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs147610678	chr6:167739868-167739869	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs547974585	chr6:167739977-167739978	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs566204871	chr6:167740022-167740023	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs554198297	chr6:167740026-167740027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs140428858	chr6:167740033-167740034	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs554913676	chr6:167740067-167740068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs536642429	chr6:167740069-167740070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs190286178	chr6:167740104-167740105	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs577442870	chr6:167740124-167740125	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs114916181	chr6:167740167-167740168	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs113348078	chr6:167740183-167740184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs149698036	chr6:167740223-167740224	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs558533432	chr6:167740249-167740250	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs386708589	chr6:167740363-167740364	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs80332431	chr6:167740364-167740365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs59072783	chr6:167740365-167740366	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs552601839	chr6:167740412-167740413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs564539886	chr6:167740440-167740441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs528492165	chr6:167740453-167740454	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs182650355	chr6:167740461-167740462	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs186972162	chr6:167740534-167740535	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs375416325	chr6:167740594-167740595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs555543684	chr6:167740618-167740619	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs529859707	chr6:167740625-167740626	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs368501860	chr6:167740651-167740652	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs569411433	chr6:167740696-167740697	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs574101136	chr6:167740739-167740740	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs545179882	chr6:167740766-167740767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs76918157	chr6:167740773-167740774	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs148825695	chr6:167740794-167740795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs2981975	chr6:167740831-167740832	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs192233333	chr6:167740861-167740862	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs34023306	chr6:167740863-167740864	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs116121586	chr6:167740873-167740874	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs143419453	chr6:167740875-167740876	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs571586773	chr6:167740926-167740927	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs377310568	chr6:167741032-167741033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs146648206	chr6:167741060-167741061	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs546284757	chr6:167741085-167741086	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs564445500	chr6:167741101-167741102	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:650 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:167737600-167739800	Enhancers	Fetal Brain Male	brain
2	chr6:167738400-167742200	Enhancers	Fetal Brain Female	brain
3	chr6:167738800-167744200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr6:167739200-167739600	Enhancers	HepG2	liver
5	chr6:167739400-167739800	Enhancers	Fetal Intestine Small	intestine
6	chr6:167739600-167741400	Weak transcription	HepG2	liver
7	chr6:167739800-167740200	Weak transcription	Fetal Brain Male	brain
8	chr6:167739800-167745200	Weak transcription	Fetal Intestine Small	intestine
9	chr6:167740200-167742800	Enhancers	Fetal Brain Male	brain
10	chr6:167740800-167742400	Enhancers	Ovary	ovary
11	chr6:167741400-167742800	Enhancers	HepG2	liver
12	chr6:167741600-167742400	Enhancers	Thymus	Thymus
13	chr6:167742200-167742600	Weak transcription	Fetal Brain Female	brain
14	chr6:167742400-167743800	Weak transcription	Ovary	ovary
15	chr6:167742600-167743200	Enhancers	Fetal Brain Female	brain
16	chr6:167742600-167750400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr6:167742800-167744200	Weak transcription	HepG2	liver
18	chr6:167742800-167751400	Weak transcription	Fetal Brain Male	brain
19	chr6:167743800-167744400	Enhancers	Ovary	ovary
20	chr6:167744000-167744200	Weak transcription	Spleen	Spleen
21	chr6:167744200-167744400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
22	chr6:167744200-167744600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr6:167744200-167744600	Enhancers	Lung	lung
24	chr6:167744200-167745400	Enhancers	Spleen	Spleen
25	chr6:167744200-167745800	Enhancers	HepG2	liver
26	chr6:167744400-167745600	Enhancers	Stomach Mucosa	stomach
27	chr6:167744600-167750000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr6:167745200-167745800	Enhancers	Fetal Intestine Small	intestine
29	chr6:167745400-167746000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr6:167745400-167750000	Weak transcription	Spleen	Spleen
31	chr6:167745600-167745800	Flanking Active TSS	Duodenum Mucosa	Duodenum
32	chr6:167745600-167745800	Enhancers	Pancreas	Pancrea
33	chr6:167745800-167750000	Weak transcription	HepG2	liver
34	chr6:167745800-167753600	Weak transcription	Pancreas	Pancrea
35	chr6:167749600-167749800	Enhancers	Fetal Thymus	thymus
36	chr6:167749600-167752400	Enhancers	Thymus	Thymus
37	chr6:167749800-167750400	Weak transcription	Fetal Thymus	thymus
38	chr6:167750000-167750400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr6:167750000-167750400	ZNF genes & repeats	Spleen	Spleen
40	chr6:167750000-167750600	Enhancers	Fetal Lung	lung
41	chr6:167750000-167751000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr6:167750000-167752600	Enhancers	HepG2	liver
43	chr6:167750400-167750600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr6:167750400-167751000	Enhancers	Liver	Liver
45	chr6:167750400-167751200	Enhancers	Fetal Thymus	thymus
46	chr6:167750400-167751400	Weak transcription	Spleen	Spleen
47	chr6:167750600-167751000	Weak transcription	Fetal Lung	lung
48	chr6:167750600-167751600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr6:167750800-167751000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr6:167751000-167751200	Enhancers	Fetal Lung	lung

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