Variant report

Variant	nsv830691
Chromosome Location	chr6:73530978-73743648
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:759)
CpG islands
(count:183)
Chromatin interactive
region (count:40)
LncRNA
region (count:1)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:759 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr6:73709826-73710035	K562	blood:	n/a	n/a
2	ATF1	chr6:73641793-73641921	K562	blood:	n/a	n/a
3	ATF1	chr6:73623605-73623783	K562	blood:	n/a	n/a
4	ATF2	chr6:73534554-73535058	GM12878	blood:	n/a	n/a
5	ATF2	chr6:73534539-73535019	GM12878	blood:	n/a	n/a
6	BACH1	chr6:73657442-73657473	K562	blood:	n/a	n/a
7	BATF	chr6:73535069-73535314	GM12878	blood:	n/a	chr6:73535192-73535203
8	BATF	chr6:73545562-73545740	GM12878	blood:	n/a	n/a
9	BATF	chr6:73665423-73665763	GM12878	blood:	n/a	n/a
10	BATF	chr6:73535014-73535356	GM12878	blood:	n/a	chr6:73535192-73535203
11	BATF	chr6:73571892-73572163	GM12878	blood:	n/a	n/a
12	BATF	chr6:73545568-73545756	GM12878	blood:	n/a	n/a
13	BCL3	chr6:73709716-73709949	GM12878	blood:	n/a	n/a
14	BRCA1	chr6:73660298-73660310	GM12878	blood:	n/a	n/a
15	BRCA1	chr6:73659875-73660669	Hela-S3	cervix:	n/a	n/a
16	CCNT2	chr6:73624524-73624724	K562	blood:	n/a	n/a
17	CEBPB	chr6:73585133-73585329	IMR90	lung:	n/a	n/a
18	CEBPB	chr6:73659783-73660373	A549	lung:	n/a	n/a
19	CEBPB	chr6:73707335-73707591	K562	blood:	n/a	n/a
20	CEBPB	chr6:73672443-73672661	K562	blood:	n/a	chr6:73672565-73672582 chr6:73672566-73672579
21	CEBPB	chr6:73677078-73677414	K562	blood:	n/a	chr6:73677232-73677243
22	CEBPB	chr6:73709322-73709537	A549	lung:	n/a	chr6:73709418-73709429
23	CEBPB	chr6:73647831-73648109	MCF-7	breast:	n/a	chr6:73648056-73648067
24	CEBPB	chr6:73656546-73656771	K562	blood:	n/a	chr6:73656637-73656648 chr6:73656638-73656649 chr6:73656637-73656650
25	CEBPB	chr6:73650167-73650459	A549	lung:	n/a	chr6:73650383-73650396
26	CEBPB	chr6:73575225-73575567	IMR90	lung:	n/a	n/a
27	CEBPB	chr6:73550978-73551274	A549	lung:	n/a	chr6:73551163-73551174
28	CEBPB	chr6:73708702-73708794	A549	lung:	n/a	chr6:73708702-73708715
29	CEBPB	chr6:73709384-73709554	H1-hESC	embryonic stem cell:	n/a	chr6:73709418-73709429
30	CEBPB	chr6:73647838-73648281	A549	lung:	n/a	chr6:73648056-73648067
31	CEBPB	chr6:73647878-73648208	A549	lung:	n/a	chr6:73648056-73648067
32	CEBPB	chr6:73647862-73648211	Hela-S3	cervix:	n/a	chr6:73648056-73648067
33	CEBPB	chr6:73677069-73677417	IMR90	lung:	n/a	chr6:73677232-73677243
34	CEBPB	chr6:73739416-73739780	K562	blood:	n/a	n/a
35	CEBPB	chr6:73715350-73715573	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr6:73707570-73707603	A549	lung:	n/a	n/a
37	CEBPB	chr6:73659873-73660628	A549	lung:	n/a	n/a
38	CEBPB	chr6:73707406-73707555	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr6:73659891-73660281	A549	lung:	n/a	n/a
40	CEBPB	chr6:73659817-73660744	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr6:73543600-73543837	IMR90	lung:	n/a	chr6:73543707-73543718
42	CEBPB	chr6:73724693-73724930	HepG2	liver:	n/a	chr6:73724855-73724866
43	CEBPB	chr6:73659797-73660342	HCT-116	colon:	n/a	n/a
44	CEBPB	chr6:73659851-73660353	IMR90	lung:	n/a	n/a
45	CEBPB	chr6:73656460-73657008	A549	lung:	n/a	chr6:73656637-73656648 chr6:73656638-73656649 chr6:73656637-73656650
46	CEBPB	chr6:73709279-73709503	HepG2	liver:	n/a	chr6:73709418-73709429
47	CEBPB	chr6:73707412-73707621	K562	blood:	n/a	n/a
48	CEBPB	chr6:73647898-73648218	HepG2	liver:	n/a	chr6:73648056-73648067
49	CEBPB	chr6:73543542-73543863	K562	blood:	n/a	chr6:73543707-73543718
50	CEBPB	chr6:73724844-73724875	H1-hESC	embryonic stem cell:	n/a	chr6:73724855-73724866

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:73697135-73697185	AoSMC	blood vessel:	n/a
2	chr6:73697178-73697228	U87	brain:	n/a
3	chr6:73738087-73738137	HNPCEpiC	eye:	n/a
4	chr6:73738087-73738137	HRCEpiC	kidney:	n/a
5	chr6:73697178-73697228	SK-N-SH	brain:	n/a
6	chr6:73697135-73697185	IMR90	lung:	fetal
7	chr6:73697135-73697185	H1-hESC	embryonic stem cell:	embryo
8	chr6:73697178-73697228	CMK	blood:	n/a
9	chr6:73697135-73697185	PrEC	prostate:	n/a
10	chr6:73697178-73697228	MCF-7	breast:	n/a
11	chr6:73697178-73697228	BJ	skin:	n/a
12	chr6:73738087-73738137	K562	blood:	n/a
13	chr6:73697135-73697185	Caco-2	colon:	n/a
14	chr6:73738087-73738137	HMEC	breast:	n/a
15	chr6:73697178-73697228	Hepatocyte	liver:	n/a
16	chr6:73738087-73738137	HIPEpiC	eye:	n/a
17	chr6:73697178-73697228	HepG2	liver:	n/a
18	chr6:73738087-73738137	HRE	kidney:	n/a
19	chr6:73697178-73697228	AG09319	gingival:	n/a
20	chr6:73697178-73697228	NHBE	bronchial:	n/a
21	chr6:73738087-73738137	Jurkat	blood:	n/a
22	chr6:73697178-73697228	Hela-S3	cervix:	n/a
23	chr6:73738087-73738137	MCF-7	breast:	n/a
24	chr6:73738087-73738137	SKMC	muscle:	n/a
25	chr6:73697178-73697228	RPTEC	kidney:	n/a
26	chr6:73697178-73697228	HNPCEpiC	eye:	n/a
27	chr6:73697178-73697228	BE2_C	brain:	n/a
28	chr6:73738087-73738137	HPAEpiC	pulmonary alveolar:	n/a
29	chr6:73697178-73697228	A549	lung:	n/a
30	chr6:73738087-73738137	NHBE	bronchial:	n/a
31	chr6:73738087-73738137	NT2-D1	testis:	n/a
32	chr6:73738087-73738137	GM19239	blood:	n/a
33	chr6:73697135-73697185	HL-60	blood:	n/a
34	chr6:73697135-73697185	AG04450	lung:	fetal
35	chr6:73697135-73697185	T-47D	breast:	n/a
36	chr6:73738087-73738137	RPTEC	kidney:	n/a
37	chr6:73738087-73738137	NB4	blood:	n/a
38	chr6:73697135-73697185	AG10803	skin:	n/a
39	chr6:73697178-73697228	AG09309	skin:	n/a
40	chr6:73697178-73697228	GM12891	blood:	n/a
41	chr6:73697135-73697185	GM12891	blood:	n/a
42	chr6:73697178-73697228	NB4	blood:	n/a
43	chr6:73697135-73697185	HEK293	kidney:	embryo
44	chr6:73697178-73697228	NHDF-neo	bronchial:	n/a
45	chr6:73697135-73697185	GM12878	blood:	n/a
46	chr6:73738087-73738137	T-47D	breast:	n/a
47	chr6:73738087-73738137	BJ	skin:	n/a
48	chr6:73697135-73697185	HEEpiC	esophagus:	n/a
49	chr6:73697135-73697185	ECC-1	luminal epithelium:	n/a
50	chr6:73697135-73697185	HCPEpiC	choroid plexus:	n/a

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:73615548..73617402-chr6:73617942..73620639,2	MCF-7	breast:
2	chr6:73725791..73728696-chr6:73728856..73731105,2	K562	blood:
3	chr6:73635330..73637431-chr6:73640282..73642642,2	K562	blood:
4	chr17:41563672..41566538-chr6:73658673..73660193,2	MCF-7	breast:
5	chr6:73634456..73636689-chr6:73637835..73640049,2	MCF-7	breast:
6	chr6:73736185..73738096-chr6:73742597..73744343,2	MCF-7	breast:
7	chr6:73736185..73738096-chr6:73742597..73744343,2	MCF-7	breast:
8	chr6:73655234..73657018-chr6:73657854..73660537,2	MCF-7	breast:
9	chr6:73677667..73679448-chr6:73682038..73684779,2	K562	blood:
10	chr6:73652529..73654943-chr6:73658012..73660027,2	K562	blood:
11	chr6:73634456..73636689-chr6:73637835..73640049,2	MCF-7	breast:
12	chr6:73330877..73331817-chr6:73737852..73738715,4	MCF-7	breast:
13	chr6:73738206..73738747-chr6:73814378..73815243,2	MCF-7	breast:
14	chr6:73615548..73617402-chr6:73617942..73620639,2	MCF-7	breast:
15	chr6:73655234..73657018-chr6:73657854..73660537,2	MCF-7	breast:
16	chr6:73644268..73646577-chr6:73652902..73655060,2	K562	blood:
17	chr6:73677667..73679448-chr6:73682038..73684779,2	K562	blood:
18	chr6:73619228..73621648-chr6:73623234..73624763,2	K562	blood:
19	chr6:73706895..73708402-chr6:73708716..73710747,2	K562	blood:
20	chr6:73644268..73646577-chr6:73652902..73655060,2	K562	blood:
21	chr6:73657119..73659540-chr6:73737347..73739182,2	MCF-7	breast:
22	chr6:73330978..73331783-chr6:73738113..73738655,2	MCF-7	breast:
23	chr6:73619228..73621648-chr6:73623234..73624763,2	K562	blood:
24	chr6:73736653..73738823-chr6:73740271..73742330,2	K562	blood:
25	chr6:73652529..73654349-chr6:73656733..73659512,2	K562	blood:
26	chr6:73665799..73668441-chr6:73673774..73676004,2	K562	blood:
27	chr6:73665799..73668441-chr6:73673774..73676004,2	K562	blood:
28	chr6:73657119..73659540-chr6:73737347..73739182,2	MCF-7	breast:
29	chr6:73616457..73619016-chr6:73623994..73625938,2	K562	blood:
30	chr6:73737865..73738687-chr6:73794476..73795161,2	MCF-7	breast:
31	chr6:73652529..73654943-chr6:73658012..73660027,2	K562	blood:
32	chr6:73334481..73336205-chr6:73704822..73706981,2	K562	blood:
33	chr6:73616457..73619016-chr6:73623994..73625938,2	K562	blood:
34	chr6:73736653..73738823-chr6:73740271..73742330,2	K562	blood:
35	chr6:73725791..73728696-chr6:73728856..73731105,2	K562	blood:
36	chr6:73635330..73637431-chr6:73640282..73642642,2	K562	blood:
37	chr6:73331290..73331817-chr6:73737852..73738715,3	MCF-7	breast:
38	chr6:73706895..73708402-chr6:73708716..73710747,2	K562	blood:
39	chr6:73676495..73679167-chr6:73681973..73685479,3	K562	blood:
40	chr6:73652529..73654349-chr6:73656733..73659512,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C6orf221-6	chr6:73696036-73697473	NONHSAT113530

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4282	chr6:73677420-73677437	MIMAT0016912

No data

Variant related genes	Relation type
KNOP1P4	TF binding region
MIR4282	TF binding region
KCNQ5	TF binding region
KNOP1P4	CpG island
MIR4282	CpG island
KCNQ5	CpG island
ENSG00000185760	chromatin interactions
ENSG00000266180	chromatin interactions

Extended variants
information (count: 7368 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:7368 , 50 per page) page: 1 2 3 4 5 6 7 ... 148

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573066380	chr6:73531003-73531004	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs187702473	chr6:73531012-73531013	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs141892155	chr6:73531100-73531101	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs545326498	chr6:73531109-73531110	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs577499366	chr6:73531171-73531172	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs544582698	chr6:73531241-73531242	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs562696558	chr6:73531243-73531244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs544097042	chr6:73531246-73531247	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs574788081	chr6:73531249-73531250	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs542311422	chr6:73531268-73531269	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs560592421	chr6:73531338-73531339	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs530775250	chr6:73531346-73531347	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs567680340	chr6:73531347-73531348	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs565159787	chr6:73531377-73531378	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs376501002	chr6:73531383-73531384	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs9360603	chr6:73531404-73531405	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs201099007	chr6:73531442-73531443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs546852207	chr6:73531508-73531509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs193098503	chr6:73531516-73531517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs147108133	chr6:73531580-73531581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs17742423	chr6:73531612-73531613	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs10943068	chr6:73531644-73531645	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs529706895	chr6:73531666-73531667	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs547852555	chr6:73531684-73531685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs2185766	chr6:73531697-73531698	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs112243029	chr6:73531703-73531704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs145483859	chr6:73531722-73531723	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs571117817	chr6:73531736-73531737	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs538119132	chr6:73531742-73531743	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs563908188	chr6:73531781-73531782	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs189140129	chr6:73531782-73531783	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs542274460	chr6:73531787-73531788	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs554293515	chr6:73531856-73531857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs572613446	chr6:73531888-73531889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs540426242	chr6:73531893-73531894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs371483978	chr6:73531982-73531983	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs532345757	chr6:73532011-73532012	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs549208465	chr6:73532032-73532033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs74498411	chr6:73532127-73532128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs562822087	chr6:73532143-73532144	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs181719197	chr6:73532156-73532157	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs74423070	chr6:73532265-73532266	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs566218447	chr6:73532328-73532329	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs527429376	chr6:73532333-73532334	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs551868110	chr6:73532365-73532366	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs116713577	chr6:73532393-73532394	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs184459218	chr6:73532401-73532402	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs188862568	chr6:73532513-73532514	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs529506885	chr6:73532567-73532568	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs3005768	chr6:73532569-73532570	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:97)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	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
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	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
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ovarian cancer	17437010	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Mental retardation	17124404	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Multiple myeloma	16616336	CNVD
Acute myeloid leukemia	16864856	CNVD
Follicular lymphoma	17699855	CNVD
Breast cancer	17133270	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Breast cancer	20409316	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1134 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:73509200-73572200	Weak transcription	Primary B cells from cord blood	blood
2	chr6:73522600-73534600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr6:73522600-73534600	Weak transcription	NHDF-Ad	bronchial
4	chr6:73527200-73531400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr6:73529200-73531000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr6:73529200-73531000	Enhancers	HMEC	breast
7	chr6:73529200-73531000	Enhancers	NHEK	skin
8	chr6:73529200-73531200	Enhancers	Dnd41	blood
9	chr6:73529200-73532400	Enhancers	Primary hematopoietic stem cells short term culture	blood
10	chr6:73529400-73531000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr6:73529400-73531200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr6:73529600-73531000	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr6:73529600-73532200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr6:73529600-73532800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr6:73529800-73531600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr6:73529800-73531800	Enhancers	Psoas Muscle	Psoas
17	chr6:73529800-73532800	Enhancers	Primary neutrophils fromperipheralblood	blood
18	chr6:73529800-73532800	Enhancers	Skeletal Muscle Female	skeletal muscle
19	chr6:73529800-73533600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr6:73529800-73534800	Weak transcription	Primary monocytes fromperipheralblood	blood
21	chr6:73530400-73531000	Enhancers	HSMMtube	muscle
22	chr6:73530600-73534400	Weak transcription	Fetal Heart	heart
23	chr6:73530600-73535200	Weak transcription	Muscle Satellite Cultured Cells	--
24	chr6:73530800-73531200	Weak transcription	HSMM	muscle
25	chr6:73530800-73531600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr6:73530800-73532400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr6:73530800-73534600	Weak transcription	Skeletal Muscle Male	skeletal muscle
28	chr6:73531000-73532200	Weak transcription	HMEC	breast
29	chr6:73531000-73532400	Weak transcription	NHEK	skin
30	chr6:73531000-73534600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr6:73531000-73535200	Weak transcription	HSMMtube	muscle
32	chr6:73531200-73532000	Enhancers	HSMM	muscle
33	chr6:73531200-73535200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr6:73531400-73531800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr6:73531600-73532200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr6:73531600-73532800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr6:73531800-73532600	Weak transcription	Psoas Muscle	Psoas
38	chr6:73531800-73535800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr6:73532000-73542200	Weak transcription	HSMM	muscle
40	chr6:73532200-73532800	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr6:73532200-73533000	Enhancers	HMEC	breast
42	chr6:73532200-73534800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr6:73532400-73532800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr6:73532400-73532800	Enhancers	NHEK	skin
45	chr6:73532400-73539800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
46	chr6:73532600-73533000	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr6:73532600-73533400	Enhancers	Psoas Muscle	Psoas
48	chr6:73532600-73533600	Enhancers	H9 Cell Line	embryonic stem cell
49	chr6:73532800-73534200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr6:73532800-73534400	Weak transcription	Skeletal Muscle Female	skeletal muscle

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