Variant report

Variant	nsv969377
Chromosome Location	chr6:30659579-30667545
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:151)
CpG islands
(count:61)
Chromatin interactive
region (count:9)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:151 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:30663144-30663454	HepG2	liver:	n/a	n/a
2	BCL3	chr6:30666797-30667017	GM12878	blood:	n/a	n/a
3	BCL3	chr6:30666778-30667080	GM12878	blood:	n/a	n/a
4	BHLHE40	chr6:30663189-30663472	HepG2	liver:	n/a	n/a
5	BHLHE40	chr6:30663213-30663514	HepG2	liver:	n/a	n/a
6	BHLHE40	chr6:30663153-30663527	HepG2	liver:	n/a	n/a
7	CEBPB	chr6:30663125-30663514	HepG2	liver:	n/a	chr6:30663299-30663310
8	CEBPB	chr6:30663138-30663389	HepG2	liver:	n/a	chr6:30663299-30663310
9	CEBPB	chr6:30663106-30663522	Hela-S3	cervix:	n/a	chr6:30663299-30663310
10	CEBPB	chr6:30663114-30663493	IMR90	lung:	n/a	chr6:30663299-30663310
11	CEBPB	chr6:30662983-30663606	HCT-116	colon:	n/a	chr6:30663299-30663310
12	CEBPB	chr6:30662927-30663609	MCF-7	breast:	n/a	chr6:30663299-30663310
13	CEBPB	chr6:30663099-30663419	A549	lung:	n/a	chr6:30663299-30663310
14	CEBPB	chr6:30662978-30663581	A549	lung:	n/a	chr6:30663299-30663310
15	CEBPB	chr6:30663145-30663476	A549	lung:	n/a	chr6:30663299-30663310
16	CEBPB	chr6:30663142-30663565	HepG2	liver:	n/a	chr6:30663299-30663310
17	CEBPB	chr6:30663121-30663495	HepG2	liver:	n/a	chr6:30663299-30663310
18	CEBPB	chr6:30662905-30663551	ECC-1	luminal epithelium:	n/a	chr6:30663299-30663310
19	CEBPB	chr6:30662918-30663613	HCT-116	colon:	n/a	chr6:30663299-30663310
20	CEBPB	chr6:30663153-30663459	K562	blood:	n/a	chr6:30663299-30663310
21	CEBPB	chr6:30663044-30663545	ECC-1	luminal epithelium:	n/a	chr6:30663299-30663310
22	CEBPB	chr6:30663129-30663478	H1-hESC	embryonic stem cell:	n/a	chr6:30663299-30663310
23	CEBPB	chr6:30663086-30663553	MCF-7	breast:	n/a	chr6:30663299-30663310
24	CEBPD	chr6:30663146-30663462	HepG2	liver:	n/a	n/a
25	CEBPD	chr6:30663105-30663498	HepG2	liver:	n/a	n/a
26	CTCF	chr6:30665359-30665423	GM13976	blood:	n/a	n/a
27	ELF1	chr6:30663192-30663402	HepG2	liver:	n/a	n/a
28	EP300	chr6:30663050-30663631	ECC-1	luminal epithelium:	n/a	n/a
29	EP300	chr6:30663098-30663434	HepG2	liver:	n/a	n/a
30	EP300	chr6:30663058-30663520	HepG2	liver:	n/a	n/a
31	EP300	chr6:30663008-30663553	HepG2	liver:	n/a	n/a
32	EP300	chr6:30663046-30663521	Hela-S3	cervix:	n/a	n/a
33	FOS	chr6:30663227-30663418	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr6:30663186-30663456	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr6:30663154-30663469	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr6:30663153-30663460	MCF10A-Er-Src	breast:	n/a	n/a
37	FOSL2	chr6:30663132-30663504	HepG2	liver:	n/a	n/a
38	FOXA1	chr6:30662981-30663427	HepG2	liver:	n/a	n/a
39	FOXA1	chr6:30663121-30663413	HepG2	liver:	n/a	n/a
40	FOXA1	chr6:30663056-30663440	HepG2	liver:	n/a	n/a
41	FOXA2	chr6:30663103-30663412	HepG2	liver:	n/a	n/a
42	GATA3	chr6:30663209-30663378	T-47D	breast:	n/a	n/a
43	GATA3	chr6:30663130-30663540	MCF-7	breast:	n/a	n/a
44	GATA3	chr6:30663104-30663432	MCF-7	breast:	n/a	n/a
45	HDAC2	chr6:30663064-30663559	HepG2	liver:	n/a	n/a
46	HDAC2	chr6:30663065-30663510	MCF-7	breast:	n/a	n/a
47	HDAC2	chr6:30663082-30663498	HepG2	liver:	n/a	n/a
48	HDAC2	chr6:30663127-30663546	MCF-7	breast:	n/a	n/a
49	HNF4A	chr6:30663177-30663392	HepG2	liver:	n/a	n/a
50	HNF4G	chr6:30663130-30663409	HepG2	liver:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:30659643-30659693	HIPEpiC	eye:	n/a
2	chr6:30659643-30659693	BJ	skin:	n/a
3	chr6:30659643-30659693	HepG2	liver:	n/a
4	chr6:30659643-30659693	NH-A	brain:	n/a
5	chr6:30659643-30659693	SK-N-SH_RA	brain:	n/a
6	chr6:30659643-30659693	HMEC	breast:	n/a
7	chr6:30659643-30659693	HL-60	blood:	n/a
8	chr6:30659643-30659693	ProgFib	skin:	n/a
9	chr6:30659643-30659693	HAEpiC	amniotic membrane:	n/a
10	chr6:30659643-30659693	SAEC	small airway:	n/a
11	chr6:30659643-30659693	AG04449	skin:	fetal
12	chr6:30659643-30659693	HPAEpiC	pulmonary alveolar:	n/a
13	chr6:30659643-30659693	CMK	blood:	n/a
14	chr6:30659643-30659693	A549	lung:	n/a
15	chr6:30659643-30659693	NT2-D1	testis:	n/a
16	chr6:30659643-30659693	Jurkat	blood:	n/a
17	chr6:30659643-30659693	AG04450	lung:	fetal
18	chr6:30659643-30659693	HRPEpiC	eye:	n/a
19	chr6:30659643-30659693	Caco-2	colon:	n/a
20	chr6:30659643-30659693	NB4	blood:	n/a
21	chr6:30659643-30659693	NHBE	bronchial:	n/a
22	chr6:30659643-30659693	HCF	heart:	n/a
23	chr6:30659643-30659693	K562	blood:	n/a
24	chr6:30659643-30659693	PFSK-1	brain:	n/a
25	chr6:30659643-30659693	IMR90	lung:	fetal
26	chr6:30659643-30659693	HCT-116	colon:	n/a
27	chr6:30659643-30659693	HRCEpiC	kidney:	n/a
28	chr6:30659643-30659693	U87	brain:	n/a
29	chr6:30659643-30659693	HEK293	kidney:	embryo
30	chr6:30659643-30659693	ECC-1	luminal epithelium:	n/a
31	chr6:30659643-30659693	AG10803	skin:	n/a
32	chr6:30659643-30659693	PrEC	prostate:	n/a
33	chr6:30659643-30659693	HUVEC	blood vessel:	n/a
34	chr6:30659643-30659693	AG09309	skin:	n/a
35	chr6:30659643-30659693	GM19239	blood:	n/a
36	chr6:30659643-30659693	RPTEC	kidney:	n/a
37	chr6:30659643-30659693	SKMC	muscle:	n/a
38	chr6:30659643-30659693	MCF10A-Er-Src	breast:	n/a
39	chr6:30659643-30659693	Hela-S3	cervix:	n/a
40	chr6:30659643-30659693	HCM	heart:	n/a
41	chr6:30659643-30659693	GM06990	blood:	n/a
42	chr6:30659643-30659693	HEEpiC	esophagus:	n/a
43	chr6:30659643-30659693	LNCaP	prostate:	n/a
44	chr6:30659643-30659693	SK-N-SH	brain:	n/a
45	chr6:30659643-30659693	AoSMC	blood vessel:	n/a
46	chr6:30659643-30659693	GM12878	blood:	n/a
47	chr6:30659643-30659693	Hepatocyte	liver:	n/a
48	chr6:30659643-30659693	HCPEpiC	choroid plexus:	n/a
49	chr6:30659643-30659693	SK-N-MC	brain:	n/a
50	chr6:30659643-30659693	MCF-7	breast:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:30643326..30660432-chr6:30681522..30696111,127	MCF-7	breast:
2	chr6:30660190..30662374-chr6:30672012..30673610,2	MCF-7	breast:
3	chr6:30580498..30587281-chr6:30649167..30662031,51	K562	blood:
4	chr6:30583469..30585601-chr6:30664144..30665970,2	K562	blood:
5	chr6:30660276..30662136-chr6:30669560..30671241,2	MCF-7	breast:
6	chr6:30634661..30668428-chr6:30680318..30698953,145	MCF-7	breast:
7	chr6:30659501..30661605-chr6:30670275..30673098,2	MCF-7	breast:
8	chr6:30652587..30660257-chr6:30673612..30681352,12	MCF-7	breast:
9	chr6:30582891..30586139-chr6:30656870..30660301,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MDC1-1	chr6:30664583-30665312	NONHSAT108667

No data

Variant related genes	Relation type
NRM	TF binding region
MDC1-AS1	TF binding region
RPL7P4	TF binding region
PPP1R18	TF binding region
NRM	CpG island
MDC1-AS1	CpG island
RPL7P4	CpG island
PPP1R18	CpG island
ENSG00000222894	chromatin interactions
ENSG00000204569	chromatin interactions
ENSG00000196230	chromatin interactions
ENSG00000224328	chromatin interactions
ENSG00000204568	chromatin interactions
ENSG00000137337	chromatin interactions
ENSG00000272540	chromatin interactions

Extended variants
information (count: 306 )
Associated
traits (count: 123 )

Variant overlapped rSNPs/rCNVs (count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562639786	chr6:30659613-30659614	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
2	rs146083525	chr6:30659660-30659661	Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
3	rs531599769	chr6:30659667-30659668	Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
4	rs181086957	chr6:30659717-30659718	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
5	rs568279524	chr6:30659733-30659734	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
6	rs561303157	chr6:30659764-30659765	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
7	rs534065125	chr6:30659784-30659785	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
8	rs140079361	chr6:30659786-30659787	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
9	rs9357100	chr6:30659810-30659811	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
10	rs147159536	chr6:30659816-30659817	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
11	rs551926510	chr6:30659818-30659819	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
12	rs570690591	chr6:30659827-30659828	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
13	rs372879825	chr6:30659904-30659905	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
14	rs539632271	chr6:30659934-30659935	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
15	rs534247866	chr6:30659977-30659978	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
16	rs56661891	chr6:30659981-30659982	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
17	rs149198070	chr6:30659982-30659983	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
18	rs371860255	chr6:30659996-30659997	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
19	rs575540380	chr6:30660007-30660008	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
20	rs556338843	chr6:30660071-30660072	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs576167009	chr6:30660078-30660079	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs535121822	chr6:30660144-30660145	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs555317870	chr6:30660181-30660182	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs544002327	chr6:30660197-30660198	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs571927902	chr6:30660236-30660237	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs563447170	chr6:30660282-30660283	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs575654987	chr6:30660298-30660299	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs370823738	chr6:30660419-30660420	Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
29	rs545894769	chr6:30660494-30660495	Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
30	rs115211008	chr6:30660501-30660502	Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
31	rs140523801	chr6:30660579-30660580	Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
32	rs376871959	chr6:30660585-30660586	Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
33	rs528455107	chr6:30660623-30660624	Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
34	rs562651589	chr6:30660624-30660625	Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
35	rs531796432	chr6:30660664-30660665	Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
36	rs540963215	chr6:30660665-30660666	Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
37	rs562359988	chr6:30660745-30660746	Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs529514369	chr6:30660809-30660810	Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs527667260	chr6:30660830-30660831	Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs547708246	chr6:30660835-30660836	Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs570753483	chr6:30660852-30660853	Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs377325180	chr6:30660878-30660879	Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs185132851	chr6:30660879-30660880	Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs527641529	chr6:30660938-30660939	Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs189548815	chr6:30660956-30660957	Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs184058318	chr6:30660957-30660958	Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs535567818	chr6:30660964-30660965	Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
48	rs555154172	chr6:30660965-30660966	Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
49	rs529088322	chr6:30660980-30660981	Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
50	rs551154295	chr6:30661007-30661008	Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:123)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
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
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	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
Melanoma	17363583	CNVD
Myelofibrosis	22110671	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
Breast cancer	21364760	CNVD
Lung cancer	21569311	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
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	CNVD
Osteosarcoma	16790693	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:312 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:30657400-30659600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr6:30657600-30659600	Flanking Active TSS	Primary hematopoietic stem cells	blood
3	chr6:30657800-30659600	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
4	chr6:30658200-30659600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
5	chr6:30658400-30659600	Active TSS	iPS-20b Cell Line	embryonic stem cell
6	chr6:30658800-30660400	Enhancers	Placenta	Placenta
7	chr6:30658800-30662400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr6:30658800-30668200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr6:30658800-30670200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr6:30658800-30670400	Weak transcription	Lung	lung
11	chr6:30659000-30659600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr6:30659000-30659600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr6:30659000-30659600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr6:30659000-30659600	Flanking Active TSS	Liver	Liver
15	chr6:30659000-30659600	Enhancers	Placenta Amnion	Placenta Amnion
16	chr6:30659000-30659600	Flanking Active TSS	A549	lung
17	chr6:30659000-30659600	Flanking Active TSS	Dnd41	blood
18	chr6:30659000-30659600	Flanking Active TSS	GM12878-XiMat	blood
19	chr6:30659000-30659600	Flanking Active TSS	NHEK	skin
20	chr6:30659000-30663600	Weak transcription	Pancreas	Pancrea
21	chr6:30659000-30669800	Weak transcription	Left Ventricle	heart
22	chr6:30659000-30670200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr6:30659000-30670200	Weak transcription	Esophagus	oesophagus
24	chr6:30659000-30670200	Weak transcription	Gastric	stomach
25	chr6:30659000-30670200	Weak transcription	Ovary	ovary
26	chr6:30659000-30670200	Weak transcription	Sigmoid Colon	Sigmoid Colon
27	chr6:30659000-30670200	Weak transcription	Spleen	Spleen
28	chr6:30659000-30670400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr6:30659000-30670800	Weak transcription	Right Ventricle	heart
30	chr6:30659200-30659600	Enhancers	H1 Cell Line	embryonic stem cell
31	chr6:30659200-30659600	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr6:30659200-30659600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr6:30659200-30659600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr6:30659200-30659600	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
35	chr6:30659200-30659600	Enhancers	Primary monocytes fromperipheralblood	blood
36	chr6:30659200-30659600	Enhancers	Primary neutrophils fromperipheralblood	blood
37	chr6:30659200-30659600	Enhancers	Primary B cells from cord blood	blood
38	chr6:30659200-30659600	Enhancers	Primary B cells from peripheral blood	blood
39	chr6:30659200-30659600	Enhancers	Primary T cells from cord blood	blood
40	chr6:30659200-30659600	Enhancers	Primary T cells fromperipheralblood	blood
41	chr6:30659200-30659600	Enhancers	Primary hematopoietic stem cells short term culture	blood
42	chr6:30659200-30659600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
43	chr6:30659200-30659600	Enhancers	Primary T helper naive cells from peripheral blood	blood
44	chr6:30659200-30659600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
45	chr6:30659200-30659600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
46	chr6:30659200-30659600	Enhancers	Primary T helper cells fromperipheralblood	blood
47	chr6:30659200-30659600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
48	chr6:30659200-30659600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
49	chr6:30659200-30659600	Enhancers	Cortex derived primary cultured neurospheres	brain
50	chr6:30659200-30659600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin

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