Variant report

Variant	nsv883545
Chromosome Location	chr6:29832332-29878738
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:496)
CpG islands
(count:4646)
Chromatin interactive
region (count:15)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:496 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:29875811-29876235	HepG2	liver:	n/a	n/a
2	ATF2	chr6:29855111-29855461	GM12878	blood:	n/a	n/a
3	BACH1	chr6:29855165-29855963	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr6:29856215-29856296	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr6:29851803-29851956	GM12878	blood:	n/a	n/a
6	BCLAF1	chr6:29855140-29855473	GM12878	blood:	n/a	n/a
7	BCLAF1	chr6:29855643-29856413	GM12878	blood:	n/a	chr6:29856154-29856163
8	BHLHE40	chr6:29854050-29854095	K562	blood:	n/a	chr6:29854055-29854064 chr6:29854054-29854063 chr6:29854052-29854065 chr6:29854054-29854063
9	BHLHE40	chr6:29855944-29856452	GM12878	blood:	n/a	n/a
10	BHLHE40	chr6:29833609-29833734	GM12878	blood:	n/a	n/a
11	BHLHE40	chr6:29855207-29855618	GM12878	blood:	n/a	n/a
12	BRCA1	chr6:29855788-29855791	Hela-S3	cervix:	n/a	n/a
13	CBX3	chr6:29849244-29849472	K562	blood:	n/a	n/a
14	CBX3	chr6:29843531-29843837	K562	blood:	n/a	n/a
15	CBX3	chr6:29849260-29849524	K562	blood:	n/a	n/a
16	CBX3	chr6:29843553-29843869	K562	blood:	n/a	n/a
17	CEBPB	chr6:29854505-29854785	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr6:29852372-29852535	K562	blood:	n/a	n/a
19	CEBPB	chr6:29875683-29875866	HepG2	liver:	n/a	n/a
20	CEBPB	chr6:29875616-29875982	HepG2	liver:	n/a	n/a
21	CEBPB	chr6:29870799-29871010	A549	lung:	n/a	n/a
22	CEBPB	chr6:29852514-29852534	A549	lung:	n/a	n/a
23	CEBPB	chr6:29855628-29855906	Hela-S3	cervix:	n/a	n/a
24	CHD1	chr6:29855282-29856146	GM12878	blood:	n/a	n/a
25	CHD2	chr6:29855925-29856000	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr6:29855118-29856258	Hela-S3	cervix:	n/a	chr6:29856140-29856147
27	CHD2	chr6:29851734-29851784	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr6:29855897-29856432	GM12878	blood:	n/a	chr6:29856140-29856147
29	CHD2	chr6:29855192-29855460	GM12878	blood:	n/a	n/a
30	CHD2	chr6:29875954-29875956	GM12878	blood:	n/a	n/a
31	CREB1	chr6:29855180-29855571	A549	lung:	n/a	n/a
32	CREB1	chr6:29855621-29856506	GM12878	blood:	n/a	n/a
33	CTCF	chr6:29855389-29855492	HepG2	liver:	n/a	n/a
34	CTCF	chr6:29840700-29840850	HepG2	liver:	n/a	n/a
35	CTCF	chr6:29855380-29855530	Caco-2	colon:	n/a	n/a
36	CTCF	chr6:29855739-29855927	GM19239	blood:	n/a	n/a
37	CTCF	chr6:29855620-29855770	HCM	heart:	n/a	n/a
38	CTCF	chr6:29855493-29855496	HepG2	liver:	n/a	n/a
39	CTCF	chr6:29855483-29855486	MCF-7	breast:	n/a	n/a
40	CTCF	chr6:29855827-29855880	GM19240	blood:	n/a	n/a
41	CTCF	chr6:29855340-29855490	AG04450	lung:	n/a	n/a
42	CTCF	chr6:29850964-29851016	GM20000	blood:	n/a	n/a
43	CTCF	chr6:29855300-29855450	HAc	cerebellar:	n/a	n/a
44	CTCF	chr6:29855405-29855450	NHEK	skin:	n/a	n/a
45	CTCF	chr6:29855340-29855490	RPTEC	kidney:	n/a	n/a
46	CTCF	chr6:29855340-29855490	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr6:29835560-29835710	WERI-Rb-1	eye:	n/a	n/a
48	CTCF	chr6:29855780-29855930	HUVEC	blood vessel:	n/a	n/a
49	CTCF	chr6:29857218-29857403	GM19239	blood:	n/a	n/a
50	CTCF	chr6:29855660-29855810	AG09309	skin:	n/a	n/a

(count:4646 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:29856430-29856480	AG04449	skin:	fetal
2	chr6:29870060-29870110	GM19239	blood:	n/a
3	chr6:29856353-29856403	ECC-1	luminal epithelium:	n/a
4	chr6:29870060-29870110	GM12891	blood:	n/a
5	chr6:29855252-29855302	IMR90	lung:	fetal
6	chr6:29854799-29854849	H1-hESC	embryonic stem cell:	embryo
7	chr6:29868900-29868950	HL-60	blood:	n/a
8	chr6:29868221-29868271	HRCEpiC	kidney:	n/a
9	chr6:29856193-29856243	GM19239	blood:	n/a
10	chr6:29855302-29855352	ProgFib	skin:	n/a
11	chr6:29856430-29856480	AG04449	skin:	fetal
12	chr6:29870060-29870110	GM19239	blood:	n/a
13	chr6:29856353-29856403	ECC-1	luminal epithelium:	n/a
14	chr6:29870060-29870110	GM12891	blood:	n/a
15	chr6:29855252-29855302	IMR90	lung:	fetal
16	chr6:29854799-29854849	H1-hESC	embryonic stem cell:	embryo
17	chr6:29868900-29868950	HL-60	blood:	n/a
18	chr6:29868221-29868271	HRCEpiC	kidney:	n/a
19	chr6:29856193-29856243	GM19239	blood:	n/a
20	chr6:29855302-29855352	ProgFib	skin:	n/a
21	chr6:29856112-29856162	PFSK-1	brain:	n/a
22	chr6:29855890-29855940	AG09309	skin:	n/a
23	chr6:29856278-29856328	HRCEpiC	kidney:	n/a
24	chr6:29856182-29856232	HMEC	breast:	n/a
25	chr6:29856538-29856588	IMR90	lung:	fetal
26	chr6:29855272-29855322	Jurkat	blood:	n/a
27	chr6:29855965-29856015	GM12878	blood:	n/a
28	chr6:29869838-29869888	HNPCEpiC	eye:	n/a
29	chr6:29854174-29854224	RPTEC	kidney:	n/a
30	chr6:29870056-29870106	IMR90	lung:	fetal
31	chr6:29855970-29856020	MCF-7	breast:	n/a
32	chr6:29854089-29854139	MCF10A-Er-Src	breast:	n/a
33	chr6:29855465-29855515	AG10803	skin:	n/a
34	chr6:29856363-29856413	PFSK-1	brain:	n/a
35	chr6:29856682-29856732	AG04450	lung:	fetal
36	chr6:29855302-29855352	SKMC	muscle:	n/a
37	chr6:29859054-29859104	HEK293	kidney:	embryo
38	chr6:29870062-29870112	HRE	kidney:	n/a
39	chr6:29854174-29854224	AG10803	skin:	n/a
40	chr6:29868221-29868271	Hepatocyte	liver:	n/a
41	chr6:29856287-29856337	H1-hESC	embryonic stem cell:	embryo
42	chr6:29863774-29863824	NHBE	bronchial:	n/a
43	chr6:29859520-29859570	PANC-1	pancreas:	n/a
44	chr6:29854089-29854139	AG10803	skin:	n/a
45	chr6:29870060-29870110	HepG2	liver:	n/a
46	chr6:29870056-29870106	CMK	blood:	n/a
47	chr6:29856141-29856191	HL-60	blood:	n/a
48	chr6:29869838-29869888	SK-N-MC	brain:	n/a
49	chr6:29855914-29855964	HRPEpiC	eye:	n/a
50	chr6:29857521-29857571	LNCaP	prostate:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr6:29841660..29844352-chr6:29848135..29850264,2	MCF-7	breast:
2	chr6:29855526..29857733-chr6:29858927..29860957,2	K562	blood:
3	chr6:29718622..29721571-chr6:29836337..29838471,2	K562	blood:
4	chr6:29841660..29844352-chr6:29848135..29850264,2	MCF-7	breast:
5	chr6:29830637..29833641-chr6:29875620..29877836,4	MCF-7	breast:
6	chr6:29860588..29861572-chr6:29915904..29916650,2	HCT-116	colon:
7	chr6:29870318..29872388-chr6:29939398..29940927,2	K562	blood:
8	chr6:29855116..29856102-chr6:31324046..31324566,2	Hela-S3	cervix:
9	chr6:29855143..29855783-chr6:29910112..29910872,2	Hela-S3	cervix:
10	chr6:29855138..29856405-chr6:31238835..31239948,4	HCT-116	colon:
11	chr6:29855342..29856127-chr6:29909881..29910650,2	HCT-116	colon:
12	chr6:29855351..29857776-chr6:29858553..29861687,4	MCF-7	breast:
13	chr6:29854712..29856936-chr6:29909499..29912386,4	MCF-7	breast:
14	chr6:29862714..29864718-chr6:29865077..29867740,2	K562	blood:
15	chr6:29855991..29858588-chr6:29944087..29945954,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RNF39-11	chr6:29867168-29868721	NONHSAT108560
2	lnc-RNF39-12	chr6:29855071-29856045	NONHSAT108557
3	lnc-HLA-A-4	chr6:29866808-29870429	NONHSAT108559

No data

Variant related genes	Relation type
MCCD1P1	TF binding region
HLA-T	TF binding region
HLA-H	TF binding region
DDX39BP1	TF binding region
HCG4P7	TF binding region
MCCD1P1	CpG island
HLA-T	CpG island
HLA-H	CpG island
DDX39BP1	CpG island
HCG4P7	CpG island
ENSG00000204525	chromatin interactions
ENSG00000206503	chromatin interactions
ENSG00000235821	chromatin interactions
ENSG00000227766	chromatin interactions
ENSG00000272236	chromatin interactions
ENSG00000204625	chromatin interactions
ENSG00000235963	chromatin interactions
ENSG00000271581	chromatin interactions
ENSG00000230521	chromatin interactions
ENSG00000206341	chromatin interactions
ENSG00000231130	chromatin interactions
ENSG00000229390	chromatin interactions

Extended variants
information (count: 2847 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:2847 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2524035	chr6:29832332-29832333	Bivalent/Poised TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs201358820	chr6:29832336-29832337	Bivalent/Poised TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs555034682	chr6:29832342-29832343	Bivalent/Poised TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs9258804	chr6:29832375-29832376	Bivalent/Poised TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs534663524	chr6:29832376-29832377	Bivalent/Poised TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs9258805	chr6:29832381-29832382	Bivalent/Poised TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs73725445	chr6:29832407-29832408	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs116827860	chr6:29832451-29832452	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs1611744	chr6:29832479-29832480	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs9258807	chr6:29832481-29832482	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs9258808	chr6:29832482-29832483	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs201404448	chr6:29832483-29832484	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs183588384	chr6:29832490-29832491	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs116742675	chr6:29832497-29832498	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs3128902	chr6:29832514-29832515	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs1611745	chr6:29832516-29832517	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs9258811	chr6:29832526-29832527	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs183693507	chr6:29832557-29832558	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs549532272	chr6:29832587-29832588	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs9258812	chr6:29832600-29832601	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs529128557	chr6:29832635-29832636	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs147147213	chr6:29832652-29832653	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs138395585	chr6:29832656-29832657	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs534593564	chr6:29832659-29832660	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs557912353	chr6:29832661-29832662	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs571347799	chr6:29832662-29832663	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs540052853	chr6:29832688-29832689	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs1611746	chr6:29832692-29832693	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs1611747	chr6:29832695-29832696	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs562554620	chr6:29832722-29832723	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs150961114	chr6:29832723-29832724	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs532738026	chr6:29832724-29832725	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs9258816	chr6:29832764-29832765	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs541014016	chr6:29832807-29832808	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs149262586	chr6:29832827-29832828	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs2734977	chr6:29832840-29832841	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs2517827	chr6:29832846-29832847	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs9468645	chr6:29832867-29832868	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs386698507	chr6:29832907-29832908	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs2975032	chr6:29832908-29832909	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs2975031	chr6:29832919-29832920	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs34939740	chr6:29832926-29832927	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs2734976	chr6:29832958-29832959	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs9258823	chr6:29832963-29832964	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs2975030	chr6:29832966-29832967	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs200676212	chr6:29832991-29832992	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs531964951	chr6:29832992-29832993	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs377036405	chr6:29832994-29832995	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs2508046	chr6:29833033-29833034	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
50	rs3128900	chr6:29833057-29833058	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:104)

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
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	21448237	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
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Breast cancer	22032731	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Retinoblastoma	16790693	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
T-cell lymphomas	19863542	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
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	19571809	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	21509527	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:596 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:29831400-29832400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
2	chr6:29831400-29832400	Bivalent Enhancer	Fetal Intestine Large	intestine
3	chr6:29831800-29832400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr6:29832000-29832400	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
5	chr6:29832000-29832400	Bivalent Enhancer	Fetal Intestine Small	intestine
6	chr6:29832200-29832400	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
7	chr6:29832200-29834000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr6:29833200-29833400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr6:29833400-29833600	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
10	chr6:29833400-29833600	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr6:29834000-29834200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr6:29834200-29834400	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr6:29834400-29834600	Bivalent Enhancer	HepG2	liver
14	chr6:29837000-29849400	Weak transcription	Fetal Intestine Small	intestine
15	chr6:29837800-29838200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr6:29837800-29838200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr6:29838200-29843000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr6:29839000-29854200	Weak transcription	Stomach Smooth Muscle	stomach
19	chr6:29840200-29841800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr6:29840800-29841200	Weak transcription	Aorta	Aorta
21	chr6:29841000-29841800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr6:29841400-29841800	ZNF genes & repeats	Aorta	Aorta
23	chr6:29843000-29843600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr6:29843600-29849800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr6:29848400-29854600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr6:29848600-29854000	Weak transcription	Fetal Intestine Large	intestine
27	chr6:29849000-29849200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr6:29849200-29854000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr6:29849400-29849600	ZNF genes & repeats	Primary Natural Killer cells fromperipheralblood	blood
30	chr6:29849400-29850000	ZNF genes & repeats	Fetal Intestine Small	intestine
31	chr6:29849600-29850200	ZNF genes & repeats	Primary B cells from peripheral blood	blood
32	chr6:29849600-29851000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
33	chr6:29849800-29850000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
34	chr6:29849800-29850200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr6:29850000-29852000	Weak transcription	H1 Cell Line	embryonic stem cell
36	chr6:29850000-29854200	Weak transcription	Fetal Intestine Small	intestine
37	chr6:29850200-29851800	Weak transcription	Primary hematopoietic stem cells	blood
38	chr6:29850200-29854000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr6:29850200-29854200	Weak transcription	Primary B cells from peripheral blood	blood
40	chr6:29850800-29854600	Weak transcription	Primary B cells from cord blood	blood
41	chr6:29851400-29854400	Weak transcription	Rectal Smooth Muscle	rectum
42	chr6:29851600-29854200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
43	chr6:29852000-29852200	Enhancers	H1 Cell Line	embryonic stem cell
44	chr6:29853000-29854800	Weak transcription	Primary hematopoietic stem cells	blood
45	chr6:29853600-29854400	Enhancers	Duodenum Mucosa	Duodenum
46	chr6:29853800-29854600	Enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr6:29854000-29854200	Enhancers	Fetal Intestine Large	intestine
48	chr6:29854000-29854200	Enhancers	GM12878-XiMat	blood
49	chr6:29854000-29854200	Enhancers	Hela-S3	cervix
50	chr6:29854000-29854200	Enhancers	Monocytes-CD14+_RO01746	blood

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