Variant report

Variant	esv3517093
Chromosome Location	chr6:33291947-33297217
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:50)
CpG islands
(count:306)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr6:33291441-33292362	GM12878	blood:	n/a	n/a
2	BCLAF1	chr6:33291673-33292307	GM12878	blood:	n/a	n/a
3	CTCF	chr6:33297020-33297170	WERI-Rb-1	eye:	n/a	n/a
4	EBF1	chr6:33292069-33292400	GM12878	blood:	n/a	chr6:33292236-33292247
5	EBF1	chr6:33291833-33292415	GM12878	blood:	n/a	chr6:33292236-33292247
6	FOS	chr6:33294271-33294480	MCF10A-Er-Src	breast:	n/a	n/a
7	FOS	chr6:33294307-33294445	MCF10A-Er-Src	breast:	n/a	n/a
8	FOS	chr6:33294245-33294465	MCF10A-Er-Src	breast:	n/a	n/a
9	FOXM1	chr6:33291717-33292380	GM12878	blood:	n/a	n/a
10	FOXM1	chr6:33290454-33292426	GM12878	blood:	n/a	n/a
11	IKZF1	chr6:33291832-33292366	GM12878	blood:	n/a	n/a
12	JUN	chr6:33294314-33294353	HepG2	liver:	n/a	n/a
13	JUND	chr6:33294250-33294465	HepG2	liver:	n/a	chr6:33294329-33294340
14	JUND	chr6:33289710-33292189	GM12878	blood:	n/a	chr6:33291020-33291029 chr6:33289933-33289942 chr6:33289932-33289941 chr6:33290833-33290842
15	MEF2A	chr6:33291951-33292380	GM12878	blood:	n/a	n/a
16	MTA3	chr6:33291663-33292321	GM12878	blood:	n/a	n/a
17	MTA3	chr6:33289315-33292314	GM12878	blood:	n/a	n/a
18	MXI1	chr6:33289631-33292178	SK-N-SH	brain:	n/a	n/a
19	MYC	chr6:33296997-33297074	MCF-7	breast:	n/a	n/a
20	NFE2	chr6:33292128-33292136	GM12878	blood:	n/a	n/a
21	NFIC	chr6:33291847-33292374	GM12878	blood:	n/a	n/a
22	NFIC	chr6:33291713-33292361	GM12878	blood:	n/a	n/a
23	NRF1	chr6:33293907-33293921	H1-hESC	embryonic stem cell:	n/a	n/a
24	PML	chr6:33291621-33292330	GM12878	blood:	n/a	n/a
25	POLR2A	chr6:33289858-33292002	HepG2	liver:	n/a	n/a
26	POLR2A	chr6:33297015-33297103	MCF-7	breast:	n/a	n/a
27	POLR2A	chr6:33297081-33297097	MCF-7	breast:	n/a	n/a
28	POLR2A	chr6:33289718-33292167	GM12891	blood:	n/a	n/a
29	POLR2A	chr6:33289855-33292052	GM12878	blood:	n/a	n/a
30	REST	chr6:33290558-33291948	HCT-116	colon:	n/a	chr6:33291345-33291355 chr6:33291319-33291328
31	REST	chr6:33290559-33292013	PFSK-1	brain:	n/a	chr6:33291345-33291355 chr6:33291319-33291328
32	REST	chr6:33291729-33292003	PANC-1	pancreas:	n/a	n/a
33	REST	chr6:33290553-33292083	PFSK-1	brain:	n/a	chr6:33291345-33291355 chr6:33291319-33291328
34	REST	chr6:33290668-33292105	PANC-1	pancreas:	n/a	chr6:33291345-33291355 chr6:33291319-33291328
35	REST	chr6:33290662-33292042	ECC-1	luminal epithelium:	n/a	chr6:33291345-33291355 chr6:33291319-33291328
36	REST	chr6:33290671-33291960	ECC-1	luminal epithelium:	n/a	chr6:33291345-33291355 chr6:33291319-33291328
37	REST	chr6:33290502-33292252	HL-60	blood:	n/a	chr6:33291345-33291355 chr6:33291319-33291328
38	RUNX3	chr6:33291720-33292280	GM12878	blood:	n/a	n/a
39	RUNX3	chr6:33291756-33292364	GM12878	blood:	n/a	n/a
40	SPI1	chr6:33291854-33292324	GM12891	blood:	n/a	n/a
41	SPI1	chr6:33291636-33292425	GM12878	blood:	n/a	chr6:33291679-33291692
42	SPI1	chr6:33291917-33292347	HL-60	blood:	n/a	n/a
43	SPI1	chr6:33292016-33292283	GM12878	blood:	n/a	n/a
44	SPI1	chr6:33291826-33292295	GM12878	blood:	n/a	n/a
45	SPI1	chr6:33291780-33292337	GM12891	blood:	n/a	n/a
46	SPI1	chr6:33291689-33292365	HL-60	blood:	n/a	n/a
47	STAT5A	chr6:33289598-33292237	GM12878	blood:	n/a	chr6:33291033-33291041 chr6:33291161-33291173
48	TCF3	chr6:33291981-33292154	GM12878	blood:	n/a	n/a
49	YY1	chr6:33291814-33292174	GM12878	blood:	n/a	n/a
50	ZNF384	chr6:33290675-33292770	GM12878	blood:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:33291937-33291987	T-47D	breast:	n/a
2	chr6:33291937-33291987	T-47D	breast:	n/a
3	chr6:33294842-33294892	Hela-S3	cervix:	n/a
4	chr6:33291947-33291997	AG04449	skin:	fetal
5	chr6:33291947-33291997	MCF-7	breast:	n/a
6	chr6:33291937-33291987	HAEpiC	amniotic membrane:	n/a
7	chr6:33292029-33292079	HIPEpiC	eye:	n/a
8	chr6:33291947-33291997	HCT-116	colon:	n/a
9	chr6:33292029-33292079	A549	lung:	n/a
10	chr6:33292029-33292079	AG09309	skin:	n/a
11	chr6:33291947-33291997	HIPEpiC	eye:	n/a
12	chr6:33291937-33291987	Hepatocyte	liver:	n/a
13	chr6:33291921-33291971	MCF10A-Er-Src	breast:	n/a
14	chr6:33291921-33291971	NHDF-neo	bronchial:	n/a
15	chr6:33291947-33291997	HUVEC	blood vessel:	n/a
16	chr6:33291937-33291987	HEEpiC	esophagus:	n/a
17	chr6:33294842-33294892	HL-60	blood:	n/a
18	chr6:33292029-33292079	GM12878	blood:	n/a
19	chr6:33294842-33294892	SK-N-SH	brain:	n/a
20	chr6:33294842-33294892	HEK293	kidney:	embryo
21	chr6:33291947-33291997	SK-N-SH_RA	brain:	n/a
22	chr6:33291921-33291971	PFSK-1	brain:	n/a
23	chr6:33291921-33291971	ovcar-3	ovarian:	n/a
24	chr6:33294842-33294892	NT2-D1	testis:	n/a
25	chr6:33291947-33291997	K562	blood:	n/a
26	chr6:33294842-33294892	NH-A	brain:	n/a
27	chr6:33294842-33294892	A549	lung:	n/a
28	chr6:33292029-33292079	HEK293	kidney:	embryo
29	chr6:33291921-33291971	HPAEpiC	pulmonary alveolar:	n/a
30	chr6:33291921-33291971	HCPEpiC	choroid plexus:	n/a
31	chr6:33294842-33294892	Caco-2	colon:	n/a
32	chr6:33291937-33291987	HCPEpiC	choroid plexus:	n/a
33	chr6:33291921-33291971	SK-N-SH_RA	brain:	n/a
34	chr6:33292029-33292079	AoSMC	blood vessel:	n/a
35	chr6:33291921-33291971	GM12891	blood:	n/a
36	chr6:33291937-33291987	PFSK-1	brain:	n/a
37	chr6:33291947-33291997	ProgFib	skin:	n/a
38	chr6:33291937-33291987	HPAEpiC	pulmonary alveolar:	n/a
39	chr6:33292029-33292079	Hepatocyte	liver:	n/a
40	chr6:33291937-33291987	NHDF-neo	bronchial:	n/a
41	chr6:33292029-33292079	NH-A	brain:	n/a
42	chr6:33291921-33291971	K562	blood:	n/a
43	chr6:33291947-33291997	AoSMC	blood vessel:	n/a
44	chr6:33291921-33291971	AoSMC	blood vessel:	n/a
45	chr6:33291937-33291987	AG09319	gingival:	n/a
46	chr6:33294842-33294892	AoSMC	blood vessel:	n/a
47	chr6:33291947-33291997	HNPCEpiC	eye:	n/a
48	chr6:33292029-33292079	NHDF-neo	bronchial:	n/a
49	chr6:33291937-33291987	GM12892	blood:	n/a
50	chr6:33294842-33294892	SK-N-MC	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr6:33290607..33292474-chr6:33296152..33298353,3	MCF-7	breast:
2	chr6:33238587..33240368-chr6:33290664..33293261,2	MCF-7	breast:
3	chr6:33247934..33250111-chr6:33290391..33292325,2	MCF-7	breast:
4	chr6:33291002..33293744-chr6:33298689..33300454,2	K562	blood:
5	chr6:33280795..33292485-chr6:33374786..33387605,31	K562	blood:
6	chr6:33285348..33292496-chr6:33357328..33361566,13	K562	blood:
7	chr6:33290607..33292474-chr6:33296152..33298353,3	MCF-7	breast:
8	chr6:33166722..33169414-chr6:33289909..33292602,2	K562	blood:
9	chr6:33285330..33286875-chr6:33295909..33298718,2	K562	blood:
10	chr6:33279489..33293095-chr6:33375317..33398824,56	K562	blood:

No data

Variant related genes	Relation type
DAXX	TF binding region
DAXX	CpG island
ENSG00000237649	chromatin interactions
ENSG00000112473	chromatin interactions
ENSG00000231500	chromatin interactions
ENSG00000202441	chromatin interactions
ENSG00000223501	chromatin interactions
ENSG00000112511	chromatin interactions
ENSG00000204231	chromatin interactions
ENSG00000236104	chromatin interactions
ENSG00000227057	chromatin interactions
ENSG00000197283	chromatin interactions
ENSG00000204209	chromatin interactions
ENSG00000112514	chromatin interactions

Extended variants
information (count: 172 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:172 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs527352524	chr6:33291998-33291999	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
2	rs553170229	chr6:33292087-33292088	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
3	rs574642137	chr6:33292135-33292136	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
4	rs541625369	chr6:33292137-33292138	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
5	rs548788092	chr6:33292169-33292170	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
6	rs541928913	chr6:33292176-33292177	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
7	rs147421321	chr6:33292182-33292183	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
8	rs139751872	chr6:33292183-33292184	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
9	rs548315479	chr6:33292246-33292247	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
10	rs563845095	chr6:33292267-33292268	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
11	rs145056963	chr6:33292303-33292304	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
12	rs371456947	chr6:33292315-33292316	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
13	rs201084227	chr6:33292325-33292326	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
14	rs535535974	chr6:33292326-33292327	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
15	rs28993578	chr6:33292342-33292343	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
16	rs530496904	chr6:33292356-33292357	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
17	rs11969869	chr6:33292368-33292369	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
18	rs189189424	chr6:33292382-33292383	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
19	rs7770021	chr6:33292400-33292401	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
20	rs139537424	chr6:33292428-33292429	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
21	rs572614773	chr6:33292505-33292506	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
22	rs377104833	chr6:33292506-33292507	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
23	rs7770218	chr6:33292535-33292536	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
24	rs3130261	chr6:33292543-33292544	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs532465348	chr6:33292564-33292565	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
26	rs60841872	chr6:33292572-33292573	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
27	rs547687195	chr6:33292626-33292627	Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs147018347	chr6:33292630-33292631	Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs145825297	chr6:33292640-33292641	Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs6935247	chr6:33292655-33292656	Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs12110842	chr6:33292690-33292691	Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs12110843	chr6:33292691-33292692	Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs529877821	chr6:33292713-33292714	Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs569781748	chr6:33292752-33292753	Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs28892581	chr6:33292847-33292848	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs558536887	chr6:33292851-33292852	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs3130101	chr6:33292888-33292889	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs140813438	chr6:33292896-33292897	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs150144393	chr6:33292909-33292910	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs182072115	chr6:33292914-33292915	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs185430026	chr6:33292915-33292916	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs3130102	chr6:33292934-33292935	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs190682745	chr6:33292939-33292940	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs574782880	chr6:33293019-33293020	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs113049645	chr6:33293083-33293084	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs574027798	chr6:33293112-33293113	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs370539649	chr6:33293142-33293143	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs557249714	chr6:33293174-33293175	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs575725892	chr6:33293221-33293222	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs545943859	chr6:33293230-33293231	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:110)

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
Acute lymphoblastic leukemia	21339820	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
Renal cell carcinoma	18765545	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
Immune disease	17576883	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	18438408	CNVD
Glioblastoma multiforme	21138945	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:189 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:33289200-33292000	Active TSS	HUES64 Cell Line	embryonic stem cell
2	chr6:33289400-33292000	Active TSS	HUES6 Cell Line	embryonic stem cell
3	chr6:33289400-33292000	Active TSS	Pancreatic Islets	Pancreatic Islet
4	chr6:33289600-33292400	Active TSS	ES-I3 Cell Line	embryonic stem cell
5	chr6:33289800-33292000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
6	chr6:33289800-33292000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr6:33289800-33292000	Active TSS	A549	lung
8	chr6:33291000-33292000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
9	chr6:33291000-33292000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
10	chr6:33291000-33292000	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
11	chr6:33291000-33292000	Flanking Active TSS	Adipose Nuclei	Adipose
12	chr6:33291000-33292000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
13	chr6:33291000-33292200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
14	chr6:33291000-33292200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr6:33291000-33292400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
16	chr6:33291000-33292400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr6:33291200-33292000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr6:33291200-33292000	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr6:33291200-33292000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
20	chr6:33291200-33292000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
21	chr6:33291200-33292000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
22	chr6:33291200-33292000	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chr6:33291200-33292000	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
24	chr6:33291200-33292000	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
25	chr6:33291200-33292000	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
26	chr6:33291200-33292000	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
27	chr6:33291200-33292000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr6:33291200-33292000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr6:33291200-33292000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr6:33291200-33292000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr6:33291200-33292000	Flanking Active TSS	Brain Anterior Caudate	brain
32	chr6:33291200-33292000	Flanking Active TSS	Fetal Brain Female	brain
33	chr6:33291200-33292000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
34	chr6:33291200-33292000	Flanking Active TSS	Stomach Smooth Muscle	stomach
35	chr6:33291200-33292000	Flanking Active TSS	HUVEC	blood vessel
36	chr6:33291200-33292000	Flanking Active TSS	NH-A	brain
37	chr6:33291200-33292200	Flanking Active TSS	Primary T cells from cord blood	blood
38	chr6:33291200-33292200	Flanking Active TSS	Primary hematopoietic stem cells	blood
39	chr6:33291200-33292200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
40	chr6:33291200-33292200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr6:33291200-33292200	Flanking Active TSS	Fetal Thymus	thymus
42	chr6:33291200-33292200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
43	chr6:33291200-33292400	Flanking Active TSS	Primary B cells from cord blood	blood
44	chr6:33291200-33292600	Flanking Active TSS	Primary B cells from peripheral blood	blood
45	chr6:33291400-33292000	Flanking Active TSS	H1 Cell Line	embryonic stem cell
46	chr6:33291400-33292000	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr6:33291400-33292000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
48	chr6:33291400-33292000	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr6:33291400-33292000	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
50	chr6:33291400-33292000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood

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