Variant report

Variant	esv2754464
Chromosome Location	chr6:167059528-167130749
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:740)
CpG islands
(count:1591)
Chromatin interactive
region (count:32)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:740 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:167089914-167090051	K562	blood:	n/a	n/a
2	ATF1	chr6:167091973-167092242	K562	blood:	n/a	n/a
3	ATF1	chr6:167106355-167106363	K562	blood:	n/a	n/a
4	BACH1	chr6:167085611-167085744	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr6:167063736-167063868	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr6:167101913-167101935	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr6:167108688-167108908	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr6:167069823-167070312	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr6:167080570-167080599	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL11A	chr6:167070244-167070488	GM12878	blood:	n/a	n/a
11	BCL3	chr6:167073673-167073994	GM12878	blood:	n/a	n/a
12	BCL3	chr6:167073691-167073910	GM12878	blood:	n/a	n/a
13	BCL3	chr6:167061092-167062010	GM12878	blood:	n/a	n/a
14	BCL3	chr6:167061042-167061975	GM12878	blood:	n/a	n/a
15	BHLHE40	chr6:167094952-167094986	K562	blood:	n/a	n/a
16	CBX3	chr6:167104382-167105236	HCT-116	colon:	n/a	chr6:167104487-167104498
17	CBX3	chr6:167104434-167105358	HCT-116	colon:	n/a	chr6:167104487-167104498
18	CEBPB	chr6:167094606-167094920	A549	lung:	n/a	chr6:167094766-167094775 chr6:167094764-167094775
19	CEBPB	chr6:167089159-167089460	K562	blood:	n/a	n/a
20	CEBPB	chr6:167089120-167089531	MCF-7	breast:	n/a	n/a
21	CEBPB	chr6:167120646-167120875	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr6:167091569-167092298	Hela-S3	cervix:	n/a	chr6:167091639-167091650 chr6:167091640-167091649 chr6:167091638-167091651 chr6:167091638-167091649
23	CEBPB	chr6:167096168-167096201	H1-hESC	embryonic stem cell:	n/a	chr6:167096174-167096185
24	CEBPB	chr6:167096087-167096315	K562	blood:	n/a	chr6:167096174-167096185
25	CEBPB	chr6:167089136-167089522	K562	blood:	n/a	n/a
26	CEBPB	chr6:167065922-167066106	HepG2	liver:	n/a	chr6:167065989-167066000
27	CEBPB	chr6:167091951-167092228	HepG2	liver:	n/a	n/a
28	CEBPB	chr6:167089197-167089344	HepG2	liver:	n/a	n/a
29	CEBPB	chr6:167096109-167096334	HepG2	liver:	n/a	chr6:167096174-167096185
30	CEBPB	chr6:167094626-167094900	HepG2	liver:	n/a	chr6:167094766-167094775 chr6:167094764-167094775
31	CEBPB	chr6:167091913-167092188	A549	lung:	n/a	n/a
32	CEBPB	chr6:167091604-167091678	HepG2	liver:	n/a	chr6:167091639-167091650 chr6:167091640-167091649 chr6:167091638-167091651 chr6:167091638-167091649
33	CEBPB	chr6:167117703-167118012	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr6:167076122-167076322	HepG2	liver:	n/a	chr6:167076175-167076186
35	CEBPB	chr6:167091526-167092351	MCF-7	breast:	n/a	chr6:167091639-167091650 chr6:167091640-167091649 chr6:167091638-167091651 chr6:167091638-167091649
36	CEBPB	chr6:167095515-167095744	IMR90	lung:	n/a	n/a
37	CHD2	chr6:167070511-167070603	HepG2	liver:	n/a	n/a
38	CREB1	chr6:167120602-167120883	H1-hESC	embryonic stem cell:	n/a	n/a
39	CREB1	chr6:167091910-167092355	HepG2	liver:	n/a	n/a
40	CTCF	chr6:167089900-167090050	MCF-7	breast:	n/a	n/a
41	CTCF	chr6:167085000-167085150	SAEC	small airway:	n/a	n/a
42	CTCF	chr6:167114644-167114722	GM13976	blood:	n/a	n/a
43	CTCF	chr6:167126520-167126575	MCF-7	breast:	n/a	n/a
44	CTCF	chr6:167120620-167120770	AG04449	skin:	n/a	n/a
45	CTCF	chr6:167120660-167120810	GM12868	blood:	n/a	n/a
46	CTCF	chr6:167089823-167090142	K562	blood:	n/a	chr6:167090093-167090111
47	CTCF	chr6:167120640-167120790	AG04450	lung:	n/a	n/a
48	CTCF	chr6:167061269-167061325	MCF-7	breast:	n/a	n/a
49	CTCF	chr6:167120620-167120770	WERI-Rb-1	eye:	n/a	n/a
50	CTCF	chr6:167126442-167126631	Gliobla	brain:	n/a	n/a

(count:1591 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:167104903-167104953	HRPEpiC	eye:	n/a
2	chr6:167116208-167116258	H1-hESC	embryonic stem cell:	embryo
3	chr6:167065446-167065496	AG10803	skin:	n/a
4	chr6:167129857-167129907	GM06990	blood:	n/a
5	chr6:167104601-167104651	GM06990	blood:	n/a
6	chr6:167104903-167104953	HRPEpiC	eye:	n/a
7	chr6:167116208-167116258	H1-hESC	embryonic stem cell:	embryo
8	chr6:167065446-167065496	AG10803	skin:	n/a
9	chr6:167129857-167129907	GM06990	blood:	n/a
10	chr6:167104601-167104651	GM06990	blood:	n/a
11	chr6:167116208-167116258	HRE	kidney:	n/a
12	chr6:167116208-167116258	U87	brain:	n/a
13	chr6:167065429-167065479	H1-hESC	embryonic stem cell:	embryo
14	chr6:167062104-167062154	ECC-1	luminal epithelium:	n/a
15	chr6:167104677-167104727	HCF	heart:	n/a
16	chr6:167070296-167070346	ovcar-3	ovarian:	n/a
17	chr6:167065376-167065426	SKMC	muscle:	n/a
18	chr6:167093129-167093179	HEK293	kidney:	embryo
19	chr6:167117898-167117948	PrEC	prostate:	n/a
20	chr6:167101267-167101317	ovcar-3	ovarian:	n/a
21	chr6:167106940-167106990	HEEpiC	esophagus:	n/a
22	chr6:167093321-167093371	T-47D	breast:	n/a
23	chr6:167070053-167070103	HAEpiC	amniotic membrane:	n/a
24	chr6:167101267-167101317	HAEpiC	amniotic membrane:	n/a
25	chr6:167062180-167062230	NHDF-neo	bronchial:	n/a
26	chr6:167062180-167062230	HMEC	breast:	n/a
27	chr6:167085508-167085558	Caco-2	colon:	n/a
28	chr6:167116288-167116338	GM12878	blood:	n/a
29	chr6:167104601-167104651	HIPEpiC	eye:	n/a
30	chr6:167085508-167085558	GM12878	blood:	n/a
31	chr6:167093321-167093371	HAEpiC	amniotic membrane:	n/a
32	chr6:167104677-167104727	AG04449	skin:	fetal
33	chr6:167116288-167116338	BJ	skin:	n/a
34	chr6:167062104-167062154	GM06990	blood:	n/a
35	chr6:167104601-167104651	HEK293	kidney:	embryo
36	chr6:167070616-167070666	AG09309	skin:	n/a
37	chr6:167062180-167062230	HUVEC	blood vessel:	n/a
38	chr6:167070296-167070346	HRCEpiC	kidney:	n/a
39	chr6:167070296-167070346	HCPEpiC	choroid plexus:	n/a
40	chr6:167106940-167106990	PANC-1	pancreas:	n/a
41	chr6:167129857-167129907	IMR90	lung:	fetal
42	chr6:167116288-167116338	SK-N-SH_RA	brain:	n/a
43	chr6:167093321-167093371	IMR90	lung:	fetal
44	chr6:167104677-167104727	HRPEpiC	eye:	n/a
45	chr6:167104903-167104953	GM19239	blood:	n/a
46	chr6:167104601-167104651	PANC-1	pancreas:	n/a
47	chr6:167101267-167101317	H1-hESC	embryonic stem cell:	embryo
48	chr6:167116288-167116338	GM19239	blood:	n/a
49	chr6:167065376-167065426	HRE	kidney:	n/a
50	chr6:167104926-167104976	HRPEpiC	eye:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:167059027..167061692-chr6:167062613..167064872,3	K562	blood:
2	chr6:167099352..167102037-chr6:167146508..167149347,2	MCF-7	breast:
3	chr6:167083479..167085354-chr6:167089213..167090920,2	K562	blood:
4	chr6:167118192..167119844-chr6:167123770..167126237,2	MCF-7	breast:
5	chr6:167094171..167096219-chr6:167102346..167104221,2	K562	blood:
6	chr6:167062835..167064756-chr6:167066345..167069061,2	K562	blood:
7	chr6:167040743..167042771-chr6:167090423..167092035,2	MCF-7	breast:
8	chr6:167082807..167084979-chr6:167087135..167090920,3	K562	blood:
9	chr6:167074591..167076523-chr6:167109521..167111565,2	K562	blood:
10	chr6:167094171..167096219-chr6:167102346..167104221,2	K562	blood:
11	chr6:167105343..167108325-chr6:167108497..167110048,2	MCF-7	breast:
12	chr6:167082807..167084979-chr6:167087135..167090920,3	K562	blood:
13	chr6:167039986..167042610-chr6:167119069..167121517,2	MCF-7	breast:
14	chr6:167120732..167121236-chr6:167185691..167186290,2	MCF-7	breast:
15	chr6:167059230..167061692-chr6:167062688..167064872,2	K562	blood:
16	chr6:167097647..167099488-chr6:167100247..167103727,3	K562	blood:
17	chr6:167083479..167085354-chr6:167089213..167090920,2	K562	blood:
18	chr6:167059027..167061692-chr6:167062613..167064872,3	K562	blood:
19	chr6:167118192..167119844-chr6:167123770..167126237,2	MCF-7	breast:
20	chr6:167075814..167078811-chr6:167080757..167083595,2	MCF-7	breast:
21	chr6:167075814..167078811-chr6:167080757..167083595,2	MCF-7	breast:
22	chr6:167059230..167061692-chr6:167062688..167064872,2	K562	blood:
23	chr6:167097647..167100107-chr6:167101291..167103727,2	K562	blood:
24	chr6:167097647..167099488-chr6:167100247..167103727,3	K562	blood:
25	chr6:167095053..167097754-chr6:167110301..167112969,2	K562	blood:
26	chr6:167095053..167097754-chr6:167110301..167112969,2	K562	blood:
27	chr6:167129723..167131439-chr6:167133367..167136362,2	K562	blood:
28	chr6:167062835..167064756-chr6:167066345..167069061,2	K562	blood:
29	chr6:167097647..167100107-chr6:167101291..167103727,2	K562	blood:
30	chr6:167074591..167076523-chr6:167109521..167111565,2	K562	blood:
31	chr6:167050618..167053160-chr6:167077513..167080245,2	K562	blood:
32	chr6:167105343..167108325-chr6:167108497..167110048,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FGFR1OP-12	chr6:167064994-167067133	NONHSAT116054

No data

Variant related genes	Relation type
ENSG00000235008	TF binding region
ENSG00000235008	CpG island
ENSG00000071242	chromatin interactions

Extended variants
information (count: 3227 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:3227 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9356502	chr6:167059528-167059529	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs76546217	chr6:167059545-167059546	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs9295358	chr6:167059626-167059627	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs541912246	chr6:167059627-167059628	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs143137764	chr6:167059629-167059630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs543538290	chr6:167059652-167059653	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs115707545	chr6:167059676-167059677	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs532579137	chr6:167059678-167059679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs146880110	chr6:167059684-167059685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs59980306	chr6:167059698-167059699	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs376225232	chr6:167059699-167059700	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs59318162	chr6:167059702-167059703	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs114138589	chr6:167059719-167059720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs374351141	chr6:167059765-167059766	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs140694831	chr6:167059790-167059791	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs554919093	chr6:167059805-167059806	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs537094296	chr6:167059823-167059824	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs552369519	chr6:167059830-167059831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs570960479	chr6:167059955-167059956	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs534824917	chr6:167059958-167059959	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs191817195	chr6:167059965-167059966	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs151101647	chr6:167059967-167059968	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs141030875	chr6:167059976-167059977	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs6935499	chr6:167060016-167060017	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs150228059	chr6:167060026-167060027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs537680909	chr6:167060033-167060034	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs576082900	chr6:167060049-167060050	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs60767138	chr6:167060073-167060074	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs374021956	chr6:167060095-167060096	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs546153052	chr6:167060096-167060097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs576843591	chr6:167060098-167060099	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs139104271	chr6:167060133-167060134	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs76905922	chr6:167060148-167060149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs530271196	chr6:167060153-167060154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs542114678	chr6:167060155-167060156	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs563666881	chr6:167060205-167060206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs6937198	chr6:167060206-167060207	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs535296284	chr6:167060258-167060259	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs570780342	chr6:167060291-167060292	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs528541124	chr6:167060362-167060363	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs141566039	chr6:167060371-167060372	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs565874640	chr6:167060384-167060385	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs112585425	chr6:167060390-167060391	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs138287236	chr6:167060407-167060408	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs569929625	chr6:167060408-167060409	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs374864674	chr6:167060412-167060413	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs9295359	chr6:167060434-167060435	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs568658472	chr6:167060465-167060466	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs529847083	chr6:167060466-167060467	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs558480672	chr6:167060476-167060477	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
Developmental delay	21147756	CNVD
Chordoma	18071362	CNVD
Glioblastoma multiforme	19435819	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
Acute lymphoblastic leukemia	18458336	CNVD
Ependymoma	20639864	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	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	chr6:167045000-167061200	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr6:167047600-167061200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr6:167054400-167061400	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr6:167054600-167061400	Weak transcription	Fetal Heart	heart
5	chr6:167054600-167061400	Weak transcription	Gastric	stomach
6	chr6:167054600-167062800	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr6:167054600-167063000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr6:167054600-167063000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr6:167054800-167061200	Weak transcription	Fetal Kidney	kidney
10	chr6:167054800-167062800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr6:167056600-167062800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr6:167057800-167069400	Weak transcription	Primary neutrophils fromperipheralblood	blood
13	chr6:167059400-167060600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr6:167059600-167061800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr6:167060000-167060800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr6:167060400-167061000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr6:167060600-167061400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr6:167060800-167061000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr6:167061000-167061200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr6:167061200-167061400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
21	chr6:167061200-167061800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr6:167061200-167061800	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
23	chr6:167061200-167061800	ZNF genes & repeats	Fetal Kidney	kidney
24	chr6:167061200-167061800	Bivalent/Poised TSS	Fetal Lung	lung
25	chr6:167061200-167061800	Enhancers	Pancreas	Pancrea
26	chr6:167061400-167061600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
27	chr6:167061400-167061800	Flanking Bivalent TSS/Enh	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr6:167061400-167061800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr6:167061400-167061800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr6:167061400-167061800	ZNF genes & repeats	Fetal Brain Male	brain
31	chr6:167061400-167061800	ZNF genes & repeats	Gastric	stomach
32	chr6:167061400-167061800	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
33	chr6:167061400-167061800	Enhancers	Skeletal Muscle Female	skeletal muscle
34	chr6:167061400-167064600	Enhancers	Fetal Heart	heart
35	chr6:167061600-167061800	ZNF genes & repeats	Esophagus	oesophagus
36	chr6:167061600-167068800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
37	chr6:167061800-167062600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr6:167061800-167063200	Weak transcription	H9 Cell Line	embryonic stem cell
39	chr6:167061800-167063200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr6:167061800-167063800	Weak transcription	Fetal Brain Male	brain
41	chr6:167061800-167064000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr6:167061800-167068800	Weak transcription	Gastric	stomach
43	chr6:167061800-167068800	Weak transcription	Pancreas	Pancrea
44	chr6:167061800-167069800	Weak transcription	Esophagus	oesophagus
45	chr6:167061800-167071000	Weak transcription	Skeletal Muscle Male	skeletal muscle
46	chr6:167061800-167071800	Weak transcription	Skeletal Muscle Female	skeletal muscle
47	chr6:167062400-167064600	Enhancers	H1 Cell Line	embryonic stem cell
48	chr6:167062600-167064200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr6:167062800-167063200	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr6:167062800-167064400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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