Variant report

Variant	esv992246
Chromosome Location	chr6:33561708-33570974
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:106)
CpG islands
(count:123)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:106 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr6:33564809-33565065	GM12878	blood:	n/a	n/a
2	BHLHE40	chr6:33564918-33564972	GM12878	blood:	n/a	n/a
3	CEBPB	chr6:33563104-33563427	A549	lung:	n/a	n/a
4	CEBPB	chr6:33563091-33563420	HepG2	liver:	n/a	n/a
5	CEBPB	chr6:33563036-33563426	A549	lung:	n/a	n/a
6	CEBPB	chr6:33563207-33563263	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr6:33568499-33568682	HepG2	liver:	n/a	n/a
8	CEBPB	chr6:33567107-33567639	ECC-1	luminal epithelium:	n/a	n/a
9	CEBPB	chr6:33566321-33566370	A549	lung:	n/a	n/a
10	CEBPB	chr6:33563106-33563607	IMR90	lung:	n/a	n/a
11	CHD2	chr6:33567224-33567463	Hela-S3	cervix:	n/a	n/a
12	CTCF	chr6:33563360-33563510	WERI-Rb-1	eye:	n/a	n/a
13	CTCF	chr6:33563380-33563530	HBMEC	blood vessel:	n/a	n/a
14	E2F6	chr6:33563274-33563493	K562	blood:	n/a	n/a
15	ELK1	chr6:33567483-33567668	Hela-S3	cervix:	n/a	n/a
16	EP300	chr6:33567388-33567791	T-47D	breast:	n/a	chr6:33567485-33567495
17	EP300	chr6:33564911-33565111	GM12878	blood:	n/a	n/a
18	EP300	chr6:33567023-33567768	ECC-1	luminal epithelium:	n/a	chr6:33567317-33567330 chr6:33567485-33567495
19	EP300	chr6:33566923-33567987	ECC-1	luminal epithelium:	n/a	chr6:33567317-33567330 chr6:33567485-33567495
20	ESR1	chr6:33567147-33567601	ECC-1	luminal epithelium:	n/a	n/a
21	ESR1	chr6:33567177-33567687	ECC-1	luminal epithelium:	n/a	n/a
22	FOS	chr6:33566885-33567219	MCF10A-Er-Src	breast:	n/a	n/a
23	FOS	chr6:33563212-33563693	MCF10A-Er-Src	breast:	n/a	n/a
24	FOS	chr6:33568693-33568762	MCF10A-Er-Src	breast:	n/a	n/a
25	FOS	chr6:33563345-33563540	MCF10A-Er-Src	breast:	n/a	n/a
26	FOS	chr6:33568724-33568829	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr6:33563322-33563567	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr6:33566881-33567734	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr6:33567578-33567682	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr6:33566864-33567715	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr6:33563231-33563689	HUVEC	blood vessel:	n/a	n/a
32	FOS	chr6:33566891-33567693	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr6:33563189-33563649	MCF10A-Er-Src	breast:	n/a	n/a
34	FOXA1	chr6:33567334-33567749	T-47D	breast:	n/a	n/a
35	FOXA1	chr6:33567227-33567671	ECC-1	luminal epithelium:	n/a	n/a
36	FOXA1	chr6:33567300-33567608	ECC-1	luminal epithelium:	n/a	n/a
37	FOXA2	chr6:33567180-33567791	A549	lung:	n/a	n/a
38	FOXA2	chr6:33567231-33567710	A549	lung:	n/a	n/a
39	FOXM1	chr6:33567010-33567778	ECC-1	luminal epithelium:	n/a	n/a
40	FOXM1	chr6:33566928-33567898	ECC-1	luminal epithelium:	n/a	n/a
41	GATA3	chr6:33567313-33567718	MCF-7	breast:	n/a	n/a
42	GATA3	chr6:33567038-33567838	MCF-7	breast:	n/a	n/a
43	GTF2F1	chr6:33567114-33567492	Hela-S3	cervix:	n/a	n/a
44	HDAC2	chr6:33567085-33567905	MCF-7	breast:	n/a	n/a
45	MAX	chr6:33567030-33567894	ECC-1	luminal epithelium:	n/a	n/a
46	MAX	chr6:33567154-33567700	Hela-S3	cervix:	n/a	n/a
47	MAX	chr6:33567066-33567937	MCF-7	breast:	n/a	n/a
48	MAX	chr6:33563194-33563599	A549	lung:	n/a	n/a
49	MAX	chr6:33567150-33567818	A549	lung:	n/a	n/a
50	MAX	chr6:33567048-33567846	ECC-1	luminal epithelium:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:33562509-33562559	HRE	kidney:	n/a
2	chr6:33562509-33562559	HRE	kidney:	n/a
3	chr6:33562509-33562559	T-47D	breast:	n/a
4	chr6:33563311-33563361	HCT-116	colon:	n/a
5	chr6:33562509-33562559	SKMC	muscle:	n/a
6	chr6:33562509-33562559	NT2-D1	testis:	n/a
7	chr6:33563311-33563361	Caco-2	colon:	n/a
8	chr6:33563311-33563361	HCPEpiC	choroid plexus:	n/a
9	chr6:33562509-33562559	HAEpiC	amniotic membrane:	n/a
10	chr6:33563311-33563361	AoSMC	blood vessel:	n/a
11	chr6:33563311-33563361	CMK	blood:	n/a
12	chr6:33562509-33562559	H1-hESC	embryonic stem cell:	embryo
13	chr6:33563311-33563361	AG04450	lung:	fetal
14	chr6:33562509-33562559	A549	lung:	n/a
15	chr6:33563311-33563361	HepG2	liver:	n/a
16	chr6:33563311-33563361	HPAEpiC	pulmonary alveolar:	n/a
17	chr6:33563311-33563361	T-47D	breast:	n/a
18	chr6:33562509-33562559	BE2_C	brain:	n/a
19	chr6:33563311-33563361	GM06990	blood:	n/a
20	chr6:33562509-33562559	HEEpiC	esophagus:	n/a
21	chr6:33563311-33563361	K562	blood:	n/a
22	chr6:33563311-33563361	GM12891	blood:	n/a
23	chr6:33562509-33562559	AG09309	skin:	n/a
24	chr6:33562509-33562559	MCF10A-Er-Src	breast:	n/a
25	chr6:33562509-33562559	HCM	heart:	n/a
26	chr6:33562509-33562559	NHBE	bronchial:	n/a
27	chr6:33563311-33563361	AG09319	gingival:	n/a
28	chr6:33563311-33563361	HRCEpiC	kidney:	n/a
29	chr6:33563311-33563361	HIPEpiC	eye:	n/a
30	chr6:33563311-33563361	HCM	heart:	n/a
31	chr6:33562509-33562559	PrEC	prostate:	n/a
32	chr6:33562509-33562559	HMEC	breast:	n/a
33	chr6:33563311-33563361	BJ	skin:	n/a
34	chr6:33562509-33562559	HL-60	blood:	n/a
35	chr6:33563311-33563361	NT2-D1	testis:	n/a
36	chr6:33563311-33563361	NHDF-neo	bronchial:	n/a
37	chr6:33563311-33563361	HCF	heart:	n/a
38	chr6:33562509-33562559	PFSK-1	brain:	n/a
39	chr6:33563311-33563361	HEK293	kidney:	embryo
40	chr6:33563311-33563361	ECC-1	luminal epithelium:	n/a
41	chr6:33563311-33563361	AG10803	skin:	n/a
42	chr6:33563311-33563361	Jurkat	blood:	n/a
43	chr6:33562509-33562559	ovcar-3	ovarian:	n/a
44	chr6:33562509-33562559	GM06990	blood:	n/a
45	chr6:33562509-33562559	HCT-116	colon:	n/a
46	chr6:33562509-33562559	RPTEC	kidney:	n/a
47	chr6:33562509-33562559	HEK293	kidney:	embryo
48	chr6:33562509-33562559	CMK	blood:	n/a
49	chr6:33563311-33563361	HL-60	blood:	n/a
50	chr6:33563311-33563361	PFSK-1	brain:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:33557038..33558663-chr6:33565418..33568204,3	K562	blood:
2	chr6:33561930..33564001-chr6:33577360..33579939,2	K562	blood:
3	chr6:33567572..33569907-chr6:33573549..33575919,2	MCF-7	breast:
4	chr6:33556983..33559426-chr6:33569915..33571800,2	MCF-7	breast:
5	chr6:33566688..33568911-chr6:33636835..33638571,2	K562	blood:
6	chr6:33556084..33559190-chr6:33561463..33564085,3	K562	blood:
7	chr6:33569313..33571736-chr6:33599981..33602556,2	K562	blood:
8	chr6:33567331..33570244-chr6:33587818..33589464,2	MCF-7	breast:
9	chr6:33562478..33565325-chr6:33572841..33575005,2	MCF-7	breast:
10	chr6:33559755..33561474-chr6:33565706..33568231,2	K562	blood:
11	chr6:33557935..33558471-chr6:33567388..33568017,2	MCF-7	breast:
12	chr6:33556929..33561530-chr6:33563084..33565973,5	MCF-7	breast:
13	chr6:33555432..33562879-chr6:33670455..33680174,12	K562	blood:
14	chr6:33561576..33563352-chr6:33589353..33591952,2	K562	blood:
15	chr6:33567428..33569467-chr6:33588119..33589840,2	MCF-7	breast:

No data

Variant related genes	Relation type
LINC00336	TF binding region
LINC00336	CpG island
ENSG00000137288	chromatin interactions
ENSG00000096433	chromatin interactions
ENSG00000197251	chromatin interactions

Extended variants
information (count: 442 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:442 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs210165	chr6:33561733-33561734	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs536532676	chr6:33561760-33561761	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs9766391	chr6:33561780-33561781	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs7759859	chr6:33561811-33561812	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs536809472	chr6:33561937-33561938	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs539168809	chr6:33561955-33561956	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs557799046	chr6:33561961-33561962	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs6457733	chr6:33561962-33561963	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs6928531	chr6:33561970-33561971	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs9461891	chr6:33561975-33561976	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs200929400	chr6:33561984-33561985	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs376264676	chr6:33562041-33562042	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs71536199	chr6:33562110-33562111	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs140510439	chr6:33562111-33562112	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs375171098	chr6:33562198-33562199	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs563767805	chr6:33562261-33562262	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs531140396	chr6:33562262-33562263	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs370647358	chr6:33562269-33562270	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs552760166	chr6:33562303-33562304	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs564596588	chr6:33562353-33562354	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs528565422	chr6:33562387-33562388	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs546712396	chr6:33562415-33562416	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs6929022	chr6:33562447-33562448	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs536201053	chr6:33562469-33562470	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs548457108	chr6:33562509-33562510	Weak transcription Active TSS Enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs377269481	chr6:33562511-33562512	Weak transcription Active TSS Enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs569803218	chr6:33562568-33562569	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs536867719	chr6:33562587-33562588	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs148235797	chr6:33562610-33562611	Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs370749620	chr6:33562640-33562641	Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs576563359	chr6:33562645-33562646	Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs374413197	chr6:33562668-33562669	Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs534389393	chr6:33562707-33562708	Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs10947410	chr6:33562709-33562710	Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs6929774	chr6:33562720-33562721	Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs141789702	chr6:33562750-33562751	Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs6930081	chr6:33562755-33562756	Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs575982571	chr6:33562758-33562759	Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs546437910	chr6:33562773-33562774	Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs146331591	chr6:33562845-33562846	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs6929819	chr6:33562854-33562855	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs540718505	chr6:33562871-33562872	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs182089814	chr6:33562906-33562907	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs545992934	chr6:33562919-33562920	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs564560326	chr6:33562931-33562932	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs529291499	chr6:33562932-33562933	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs186724863	chr6:33562947-33562948	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs191490710	chr6:33562970-33562971	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs6902359	chr6:33562975-33562976	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs573071370	chr6:33563017-33563018	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Hepatocellular carcinoma	16750200	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
abnormal development	18461090	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Systemic lupus erythematosus	19279649	CNVD
Retinoblastoma	16790693	CNVD
Acute myocardial infarction	18032375	CNVD
Renal cell carcinoma	19150565	CNVD
Systemic lupus erythematosus	19591781	CNVD
Attention deficit hyperactivity disorder	19287146	CNVD
Autism	19287146	CNVD
Erythema nodosum in leprosy	19287146	CNVD
Henoch-schoenlein purpura	19287146	CNVD
Liver cirrhosis	19287146	CNVD
Systemic lupus erythematosus	19287146	CNVD
Autoimmune disease	19135723	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	CNVD
Osteosarcoma	16790693	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
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Myelofibrosis	22110671	CNVD
Incontinentia Pigmenti	22033527	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Encephalopathy	20692195	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:246 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:33558600-33567200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr6:33559000-33567200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr6:33559400-33562600	Weak transcription	A549	lung
4	chr6:33559400-33563000	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr6:33559400-33567200	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr6:33559600-33563000	Weak transcription	Hela-S3	cervix
7	chr6:33559600-33569800	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr6:33559800-33562600	Weak transcription	HepG2	liver
9	chr6:33561200-33561800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr6:33561200-33562400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr6:33561200-33563000	Weak transcription	NHDF-Ad	bronchial
12	chr6:33561200-33567200	Weak transcription	Left Ventricle	heart
13	chr6:33561400-33562000	Enhancers	Primary T cells fromperipheralblood	blood
14	chr6:33561400-33562400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr6:33561400-33562600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr6:33561400-33562600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr6:33561400-33562600	Weak transcription	Spleen	Spleen
18	chr6:33561400-33564800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
19	chr6:33561400-33564800	Weak transcription	HUVEC	blood vessel
20	chr6:33561400-33565000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr6:33561400-33565600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr6:33561400-33565600	Weak transcription	Right Ventricle	heart
23	chr6:33561400-33565600	Weak transcription	HMEC	breast
24	chr6:33561400-33567200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr6:33561400-33567200	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chr6:33561400-33567200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr6:33561400-33567200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr6:33561400-33567200	Weak transcription	Esophagus	oesophagus
29	chr6:33561400-33567200	Weak transcription	Gastric	stomach
30	chr6:33561400-33567200	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr6:33561400-33567200	Weak transcription	NH-A	brain
32	chr6:33561600-33562000	Enhancers	Primary B cells from cord blood	blood
33	chr6:33561600-33562200	Enhancers	Primary B cells from peripheral blood	blood
34	chr6:33561600-33562600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr6:33561600-33563000	Weak transcription	NHEK	skin
36	chr6:33561600-33564200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr6:33561600-33564200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr6:33561600-33564200	Weak transcription	GM12878-XiMat	blood
39	chr6:33561600-33564600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
40	chr6:33561600-33564800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
41	chr6:33561600-33564800	Weak transcription	Primary T cells from cord blood	blood
42	chr6:33561600-33564800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
43	chr6:33561600-33564800	Weak transcription	Fetal Thymus	thymus
44	chr6:33561600-33565000	Weak transcription	Duodenum Mucosa	Duodenum
45	chr6:33561600-33565800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
46	chr6:33561600-33565800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
47	chr6:33561600-33565800	Weak transcription	Fetal Intestine Small	intestine
48	chr6:33561600-33567000	Weak transcription	Primary T helper cells PMA-I stimulated	--
49	chr6:33561600-33567200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
50	chr6:33561600-33567200	Weak transcription	Rectal Mucosa Donor 29	rectum

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