Variant report

Variant	nsv1015397
Chromosome Location	chr6:32429594-32518757
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:661)
CpG islands
(count:2382)
Chromatin interactive
region (count:20)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:661 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr6:32443384-32443601	K562	blood:	n/a	n/a
2	ATF1	chr6:32441356-32441603	K562	blood:	n/a	n/a
3	ATF2	chr6:32430245-32430782	GM12878	blood:	n/a	n/a
4	ATF2	chr6:32430276-32430774	GM12878	blood:	n/a	n/a
5	BACH1	chr6:32440601-32440675	K562	blood:	n/a	n/a
6	BATF	chr6:32441263-32441838	GM12878	blood:	n/a	n/a
7	BATF	chr6:32497788-32498190	GM12878	blood:	n/a	n/a
8	BATF	chr6:32498191-32498485	GM12878	blood:	n/a	n/a
9	BATF	chr6:32430225-32430811	GM12878	blood:	n/a	n/a
10	BATF	chr6:32430260-32430743	GM12878	blood:	n/a	n/a
11	BCL11A	chr6:32430360-32430746	GM12878	blood:	n/a	chr6:32430439-32430448 chr6:32430485-32430494
12	BCL11A	chr6:32497757-32498420	GM12878	blood:	n/a	n/a
13	BCL3	chr6:32430394-32430814	GM12878	blood:	n/a	chr6:32430439-32430448 chr6:32430485-32430494
14	BCLAF1	chr6:32440393-32441925	GM12878	blood:	n/a	n/a
15	BCLAF1	chr6:32430238-32430769	GM12878	blood:	n/a	chr6:32430439-32430448 chr6:32430485-32430494
16	BCLAF1	chr6:32497233-32498192	GM12878	blood:	n/a	n/a
17	BCLAF1	chr6:32440374-32441401	GM12878	blood:	n/a	n/a
18	BCLAF1	chr6:32497559-32498097	GM12878	blood:	n/a	n/a
19	BHLHE40	chr6:32517788-32517836	K562	blood:	n/a	n/a
20	BHLHE40	chr6:32441347-32441706	GM12878	blood:	n/a	n/a
21	BHLHE40	chr6:32430364-32430844	GM12878	blood:	n/a	n/a
22	BHLHE40	chr6:32498065-32498253	GM12878	blood:	n/a	n/a
23	BHLHE40	chr6:32493926-32494025	GM12878	blood:	n/a	n/a
24	CEBPB	chr6:32441263-32441593	K562	blood:	n/a	chr6:32441418-32441431
25	CEBPB	chr6:32498060-32498200	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr6:32441238-32441567	K562	blood:	n/a	chr6:32441418-32441431
27	CEBPB	chr6:32441285-32441529	K562	blood:	n/a	chr6:32441418-32441431
28	CEBPB	chr6:32443372-32443570	K562	blood:	n/a	n/a
29	CEBPB	chr6:32441368-32441573	H1-hESC	embryonic stem cell:	n/a	chr6:32441418-32441431
30	CEBPB	chr6:32441175-32441630	MCF-7	breast:	n/a	chr6:32441418-32441431
31	CEBPB	chr6:32498063-32498112	K562	blood:	n/a	n/a
32	CEBPB	chr6:32504062-32504262	A549	lung:	n/a	n/a
33	CEBPB	chr6:32439228-32439505	HepG2	liver:	n/a	n/a
34	CEBPB	chr6:32441197-32441569	MCF-7	breast:	n/a	chr6:32441418-32441431
35	CHD1	chr6:32439451-32439466	GM12878	blood:	n/a	n/a
36	CHD1	chr6:32440915-32441307	GM12878	blood:	n/a	n/a
37	CHD1	chr6:32441573-32441770	GM12878	blood:	n/a	n/a
38	CHD1	chr6:32497360-32498091	GM12878	blood:	n/a	n/a
39	CHD2	chr6:32430457-32430741	GM12878	blood:	n/a	n/a
40	CHD2	chr6:32441156-32441715	GM12878	blood:	n/a	n/a
41	CHD2	chr6:32440569-32440726	GM12878	blood:	n/a	n/a
42	CHD2	chr6:32497862-32498076	GM12878	blood:	n/a	n/a
43	CREB1	chr6:32441162-32441776	GM12878	blood:	n/a	n/a
44	CREB1	chr6:32441253-32441662	H1-hESC	embryonic stem cell:	n/a	n/a
45	CREB1	chr6:32440638-32441803	GM12878	blood:	n/a	n/a
46	CREB1	chr6:32497839-32498347	GM12878	blood:	n/a	n/a
47	CREB1	chr6:32430254-32430970	GM12878	blood:	n/a	n/a
48	CTCF	chr6:32497921-32498032	GM19239	blood:	n/a	n/a
49	CTCF	chr6:32445635-32445846	K562	blood:	n/a	n/a
50	CTCF	chr6:32490644-32490657	MCF-7	breast:	n/a	n/a

(count:2382 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:32492198-32492248	MCF10A-Er-Src	breast:	n/a
2	chr6:32492198-32492248	HIPEpiC	eye:	n/a
3	chr6:32515150-32515200	HL-60	blood:	n/a
4	chr6:32492198-32492248	MCF10A-Er-Src	breast:	n/a
5	chr6:32492198-32492248	HIPEpiC	eye:	n/a
6	chr6:32515150-32515200	HL-60	blood:	n/a
7	chr6:32489553-32489603	Caco-2	colon:	n/a
8	chr6:32496326-32496376	AG09319	gingival:	n/a
9	chr6:32515251-32515301	HL-60	blood:	n/a
10	chr6:32499368-32499418	HCT-116	colon:	n/a
11	chr6:32489555-32489605	HL-60	blood:	n/a
12	chr6:32495746-32495796	SK-N-SH_RA	brain:	n/a
13	chr6:32489984-32490034	Hela-S3	cervix:	n/a
14	chr6:32489553-32489603	MCF-7	breast:	n/a
15	chr6:32515815-32515865	NH-A	brain:	n/a
16	chr6:32498493-32498543	NB4	blood:	n/a
17	chr6:32489984-32490034	ECC-1	luminal epithelium:	n/a
18	chr6:32490444-32490494	HCPEpiC	choroid plexus:	n/a
19	chr6:32515773-32515823	Hela-S3	cervix:	n/a
20	chr6:32489553-32489603	HEEpiC	esophagus:	n/a
21	chr6:32499852-32499902	GM12891	blood:	n/a
22	chr6:32487314-32487364	AG04449	skin:	fetal
23	chr6:32466447-32466497	Jurkat	blood:	n/a
24	chr6:32499860-32499910	NT2-D1	testis:	n/a
25	chr6:32490350-32490400	SK-N-SH_RA	brain:	n/a
26	chr6:32452388-32452438	HUVEC	blood vessel:	n/a
27	chr6:32516004-32516054	T-47D	breast:	n/a
28	chr6:32515815-32515865	IMR90	lung:	fetal
29	chr6:32515251-32515301	AoSMC	blood vessel:	n/a
30	chr6:32490421-32490471	BE2_C	brain:	n/a
31	chr6:32466447-32466497	CMK	blood:	n/a
32	chr6:32515150-32515200	HRPEpiC	eye:	n/a
33	chr6:32489801-32489851	HCT-116	colon:	n/a
34	chr6:32493917-32493967	SK-N-SH_RA	brain:	n/a
35	chr6:32498285-32498335	AG09309	skin:	n/a
36	chr6:32449961-32450011	HIPEpiC	eye:	n/a
37	chr6:32493917-32493967	Hepatocyte	liver:	n/a
38	chr6:32489801-32489851	NT2-D1	testis:	n/a
39	chr6:32487314-32487364	GM06990	blood:	n/a
40	chr6:32492198-32492248	AG09309	skin:	n/a
41	chr6:32515815-32515865	AG09309	skin:	n/a
42	chr6:32466447-32466497	H1-hESC	embryonic stem cell:	embryo
43	chr6:32515069-32515119	BJ	skin:	n/a
44	chr6:32487314-32487364	HRPEpiC	eye:	n/a
45	chr6:32490350-32490400	AoSMC	blood vessel:	n/a
46	chr6:32486399-32486449	HRPEpiC	eye:	n/a
47	chr6:32466447-32466497	NT2-D1	testis:	n/a
48	chr6:32491826-32491876	RPTEC	kidney:	n/a
49	chr6:32490421-32490471	AG09309	skin:	n/a
50	chr6:32490350-32490400	HUVEC	blood vessel:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:32432882..32434661-chr6:32437882..32440556,2	K562	blood:
2	chr6:32488425..32491082-chr6:32525421..32528152,2	MCF-7	breast:
3	chr6:32428191..32430542-chr6:32458841..32460810,2	MCF-7	breast:
4	chr6:32086283..32087229-chr6:32443372..32443883,2	K562	blood:
5	chr6:32428020..32430346-chr6:32430638..32433347,2	K562	blood:
6	chr6:32497873..32498399-chr6:32557101..32557832,2	HCT-116	colon:
7	chr6:32428191..32430542-chr6:32458841..32460810,2	MCF-7	breast:
8	chr6:32492411..32495450-chr6:32552484..32555959,3	MCF-7	breast:
9	chr6:32496441..32498666-chr6:32501268..32503290,2	MCF-7	breast:
10	chr6:32489338..32491320-chr6:32492335..32495194,2	MCF-7	breast:
11	chr6:32383034..32383683-chr6:32443303..32444621,3	MCF-7	breast:
12	chr6:32489338..32491320-chr6:32492335..32495194,2	MCF-7	breast:
13	chr6:32399459..32400332-chr6:32443390..32444188,2	MCF-7	breast:
14	chr6:32428020..32430346-chr6:32430638..32433347,2	K562	blood:
15	chr6:32446571..32447329-chr6:32534338..32534901,2	MCF-7	breast:
16	chr6:32432882..32434661-chr6:32437882..32440556,2	K562	blood:
17	chr6:32400824..32401535-chr6:32443504..32444248,2	MCF-7	breast:
18	chr6:32483984..32486232-chr6:32528948..32530708,2	MCF-7	breast:
19	chr6:32409031..32411738-chr6:32430309..32432533,2	MCF-7	breast:
20	chr6:32478863..32481240-chr6:32540968..32542884,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HLA-DRA-5	chr6:32475256-32475512	NONHSAT108909
2	lnc-HLA-DRB5-1	chr6:32441202-32441277	NONHSAT108907
3	lnc-HLA-DQA1-7	chr6:32487174-32487196	NONHSAT108910
4	lnc-HLA-DRA-4	chr6:32474307-32474692	NONHSAT108908

No data

Variant related genes	Relation type
RNU1-61P	TF binding region
HLA-DRB9	TF binding region
HLA-DRB5	TF binding region
RNU1-61P	CpG island
HLA-DRB9	CpG island
HLA-DRB5	CpG island
ENSG00000196126	chromatin interactions
ENSG00000229391	chromatin interactions
ENSG00000198502	chromatin interactions

Extended variants
information (count: 5751 )
Associated
traits (count: 131 )

Variant overlapped rSNPs/rCNVs (count:5751 , 50 per page) page: 1 2 3 4 5 6 7 ... 116

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9268852	chr6:32429594-32429595	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs9268853	chr6:32429643-32429644	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
3	rs9268854	chr6:32429672-32429673	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs9268855	chr6:32429675-32429676	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs562178598	chr6:32429685-32429686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs12527323	chr6:32429694-32429695	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs577025025	chr6:32429698-32429699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs9268856	chr6:32429719-32429720	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
9	rs183246718	chr6:32429720-32429721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs9268857	chr6:32429739-32429740	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs9268858	chr6:32429758-32429759	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs573149368	chr6:32429804-32429805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs201181224	chr6:32429810-32429811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs571313539	chr6:32429816-32429817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs371081337	chr6:32429819-32429820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs60287615	chr6:32429822-32429823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs9268860	chr6:32429825-32429826	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs377214499	chr6:32429862-32429863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs577979134	chr6:32429870-32429871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs9268861	chr6:32429894-32429895	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs140148007	chr6:32429961-32429962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs572947457	chr6:32430067-32430068	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs548292713	chr6:32430096-32430097	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs373101524	chr6:32430142-32430143	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs9268862	chr6:32430167-32430168	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs561587141	chr6:32430183-32430184	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs573583803	chr6:32430196-32430197	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs544127671	chr6:32430272-32430273	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs74473385	chr6:32430276-32430277	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs9268863	chr6:32430289-32430290	Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs9268864	chr6:32430326-32430327	Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs13193827	chr6:32430337-32430338	Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs527425107	chr6:32430358-32430359	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs4428528	chr6:32430362-32430363	Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs58302219	chr6:32430368-32430369	Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs538515021	chr6:32430421-32430422	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs375428823	chr6:32430449-32430450	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs4434496	chr6:32430508-32430509	Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs62403109	chr6:32430521-32430522	Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs554186624	chr6:32430540-32430541	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs572438561	chr6:32430564-32430565	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs564724157	chr6:32430565-32430566	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs536382003	chr6:32430569-32430570	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs555120666	chr6:32430591-32430592	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs4280993	chr6:32430604-32430605	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs113095223	chr6:32430628-32430629	Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs374245873	chr6:32430696-32430697	Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs544065801	chr6:32430711-32430712	Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs113133861	chr6:32430724-32430725	Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs377267645	chr6:32430726-32430727	Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:131)

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
Lung cancer	18438408	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
Breast cancer	22844521	CNVD
Gestational infection	22844521	CNVD
HIV/AIDS	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	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
Ovarian cancer	21781307	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
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
Acute lymphoblastic leukemia	22237106	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
Immune disease	17576883	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	22522925	CNVD
Rheumatoid arthritis	22536334	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:361 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:32428400-32430000	Weak transcription	GM12878-XiMat	blood
2	chr6:32430000-32430200	Enhancers	GM12878-XiMat	blood
3	chr6:32430200-32430600	Flanking Active TSS	GM12878-XiMat	blood
4	chr6:32430600-32431400	Active TSS	GM12878-XiMat	blood
5	chr6:32437600-32441000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr6:32439200-32439400	Active TSS	Primary B cells from peripheral blood	blood
7	chr6:32439200-32439400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr6:32439200-32439400	Active TSS	GM12878-XiMat	blood
9	chr6:32439200-32439400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
10	chr6:32439200-32439600	Active TSS	Primary T regulatory cells fromperipheralblood	blood
11	chr6:32439200-32440800	Active TSS	Primary B cells from cord blood	blood
12	chr6:32439400-32439600	Bivalent/Poised TSS	Primary Natural Killer cells fromperipheralblood	blood
13	chr6:32439400-32439600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr6:32439400-32439600	Active TSS	Monocytes-CD14+_RO01746	blood
15	chr6:32439400-32439800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr6:32439400-32440000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr6:32439400-32440200	Active TSS	Primary monocytes fromperipheralblood	blood
18	chr6:32439400-32440200	Flanking Active TSS	Primary B cells from peripheral blood	blood
19	chr6:32439400-32440800	ZNF genes & repeats	GM12878-XiMat	blood
20	chr6:32439600-32440200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr6:32439600-32441000	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
22	chr6:32439600-32442200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
23	chr6:32439800-32440600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr6:32440200-32440400	Active TSS	Primary B cells from peripheral blood	blood
25	chr6:32440200-32440800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr6:32440200-32441000	Active TSS	Primary hematopoietic stem cells short term culture	blood
27	chr6:32440200-32441200	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
28	chr6:32440200-32441800	Enhancers	Primary hematopoietic stem cells	blood
29	chr6:32440400-32442200	Flanking Active TSS	Primary B cells from peripheral blood	blood
30	chr6:32440600-32441000	Active TSS	Adipose Nuclei	Adipose
31	chr6:32440600-32441800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr6:32440600-32441800	Active TSS	Brain Anterior Caudate	brain
33	chr6:32440800-32441200	Flanking Active TSS	Primary B cells from cord blood	blood
34	chr6:32440800-32441400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr6:32440800-32442200	Flanking Active TSS	GM12878-XiMat	blood
36	chr6:32441000-32441200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr6:32441000-32441400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr6:32441000-32441400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr6:32441000-32441400	Flanking Active TSS	Adipose Nuclei	Adipose
40	chr6:32441000-32441400	Enhancers	Fetal Thymus	thymus
41	chr6:32441000-32441800	Enhancers	Duodenum Mucosa	Duodenum
42	chr6:32441000-32441800	Active TSS	Rectal Mucosa Donor 29	rectum
43	chr6:32441000-32441800	Enhancers	Spleen	Spleen
44	chr6:32441000-32442200	Enhancers	Primary hematopoietic stem cells short term culture	blood
45	chr6:32441000-32442400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
46	chr6:32441200-32441400	Enhancers	Colonic Mucosa	Colon
47	chr6:32441200-32442200	Enhancers	Primary B cells from cord blood	blood
48	chr6:32441200-32442800	Enhancers	Primary monocytes fromperipheralblood	blood
49	chr6:32441400-32441600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr6:32441600-32441800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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