Variant report

Variant	nsv521632
Chromosome Location	chr17:45151549-45196190
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:548)
CpG islands
(count:549)
Chromatin interactive
region (count:24)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:548 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:45165062-45165080	K562	blood:	n/a	n/a
2	ARID3A	chr17:45178080-45178088	HepG2	liver:	n/a	n/a
3	ARID3A	chr17:45191135-45191603	K562	blood:	n/a	n/a
4	ATF1	chr17:45176347-45176414	K562	blood:	n/a	n/a
5	BACH1	chr17:45191283-45191331	K562	blood:	n/a	n/a
6	BACH1	chr17:45177408-45177655	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL3	chr17:45177585-45178094	A549	lung:	n/a	n/a
8	BCLAF1	chr17:45177412-45177731	GM12878	blood:	n/a	n/a
9	BHLHE40	chr17:45176257-45176572	K562	blood:	n/a	n/a
10	BHLHE40	chr17:45177528-45177799	GM12878	blood:	n/a	n/a
11	BHLHE40	chr17:45176199-45176524	GM12878	blood:	n/a	n/a
12	BHLHE40	chr17:45177425-45177752	K562	blood:	n/a	n/a
13	BRCA1	chr17:45177718-45177810	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr17:45176116-45176464	K562	blood:	n/a	n/a
15	CBX3	chr17:45183455-45183828	K562	blood:	n/a	n/a
16	CCNT2	chr17:45177380-45177744	K562	blood:	n/a	chr17:45177652-45177661
17	CEBPB	chr17:45186765-45187032	Hela-S3	cervix:	n/a	chr17:45186889-45186900
18	CEBPB	chr17:45186544-45187072	A549	lung:	n/a	chr17:45186889-45186900
19	CEBPB	chr17:45186716-45187064	K562	blood:	n/a	chr17:45186889-45186900
20	CEBPB	chr17:45186740-45186992	A549	lung:	n/a	chr17:45186889-45186900
21	CEBPB	chr17:45179693-45179787	HepG2	liver:	n/a	chr17:45179737-45179748
22	CEBPB	chr17:45179721-45179888	A549	lung:	n/a	chr17:45179737-45179748
23	CEBPB	chr17:45186735-45187052	HepG2	liver:	n/a	chr17:45186889-45186900
24	CEBPB	chr17:45153563-45153819	IMR90	lung:	n/a	n/a
25	CEBPD	chr17:45183555-45183952	K562	blood:	n/a	n/a
26	CEBPD	chr17:45177335-45177879	HepG2	liver:	n/a	n/a
27	CEBPZ	chr17:45177620-45177795	HepG2	liver:	n/a	n/a
28	CHD1	chr17:45177363-45177588	GM12878	blood:	n/a	n/a
29	CHD2	chr17:45177441-45177829	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr17:45177505-45177823	HepG2	liver:	n/a	n/a
31	CHD2	chr17:45177530-45177902	K562	blood:	n/a	n/a
32	CHD2	chr17:45177434-45177950	GM12878	blood:	n/a	n/a
33	CHD2	chr17:45177396-45177943	Hela-S3	cervix:	n/a	n/a
34	CREB1	chr17:45177184-45177885	A549	lung:	n/a	n/a
35	CREB1	chr17:45177555-45177825	A549	lung:	n/a	n/a
36	CREB1	chr17:45177262-45177977	HepG2	liver:	n/a	n/a
37	CTCF	chr17:45177440-45177590	GM12873	blood:	n/a	n/a
38	CTCF	chr17:45177440-45177590	GM12864	blood:	n/a	n/a
39	CTCF	chr17:45161375-45161457	GM10266	blood:	n/a	n/a
40	CTCF	chr17:45177640-45177766	Kidney_OC	kidney:	n/a	n/a
41	CTCF	chr17:45192967-45193078	GM10248	blood:	n/a	n/a
42	CTCF	chr17:45177460-45177610	GM12872	blood:	n/a	n/a
43	CTCF	chr17:45177460-45177610	GM12875	blood:	n/a	n/a
44	CTCF	chr17:45177440-45177590	HRE	kidney:	n/a	n/a
45	CTCF	chr17:45177480-45177630	AG04449	skin:	n/a	n/a
46	CTCF	chr17:45177480-45177630	Caco-2	colon:	n/a	n/a
47	CTCF	chr17:45190572-45190702	Kidney_OC	kidney:	n/a	n/a
48	CTCF	chr17:45177460-45177610	HEK293	kidney:	n/a	n/a
49	CTCF	chr17:45177440-45177590	HUVEC	blood vessel:	n/a	n/a
50	CTCF	chr17:45177558-45177691	Lung_OC	lung:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:45174155-45174205	HMEC	breast:	n/a
2	chr17:45177859-45177909	BJ	skin:	n/a
3	chr17:45177378-45177428	HRPEpiC	eye:	n/a
4	chr17:45180460-45180510	Jurkat	blood:	n/a
5	chr17:45177628-45177678	Caco-2	colon:	n/a
6	chr17:45177429-45177479	HRPEpiC	eye:	n/a
7	chr17:45177431-45177481	NH-A	brain:	n/a
8	chr17:45180460-45180510	GM12892	blood:	n/a
9	chr17:45177598-45177648	ECC-1	luminal epithelium:	n/a
10	chr17:45177598-45177648	NHDF-neo	bronchial:	n/a
11	chr17:45177431-45177481	HMEC	breast:	n/a
12	chr17:45177598-45177648	SKMC	muscle:	n/a
13	chr17:45180460-45180510	AG04450	lung:	fetal
14	chr17:45177859-45177909	T-47D	breast:	n/a
15	chr17:45177431-45177481	ovcar-3	ovarian:	n/a
16	chr17:45177429-45177479	AG09319	gingival:	n/a
17	chr17:45177378-45177428	HEEpiC	esophagus:	n/a
18	chr17:45180460-45180510	CMK	blood:	n/a
19	chr17:45183984-45184034	HNPCEpiC	eye:	n/a
20	chr17:45177628-45177678	AoSMC	blood vessel:	n/a
21	chr17:45183984-45184034	BJ	skin:	n/a
22	chr17:45174155-45174205	PANC-1	pancreas:	n/a
23	chr17:45177628-45177678	T-47D	breast:	n/a
24	chr17:45177598-45177648	SK-N-SH_RA	brain:	n/a
25	chr17:45174155-45174205	ovcar-3	ovarian:	n/a
26	chr17:45177628-45177678	IMR90	lung:	fetal
27	chr17:45177378-45177428	PrEC	prostate:	n/a
28	chr17:45180460-45180510	HNPCEpiC	eye:	n/a
29	chr17:45180460-45180510	AG04449	skin:	fetal
30	chr17:45177429-45177479	SK-N-SH_RA	brain:	n/a
31	chr17:45174155-45174205	ECC-1	luminal epithelium:	n/a
32	chr17:45177598-45177648	ProgFib	skin:	n/a
33	chr17:45177598-45177648	HEEpiC	esophagus:	n/a
34	chr17:45180460-45180510	HMEC	breast:	n/a
35	chr17:45174155-45174205	GM06990	blood:	n/a
36	chr17:45180460-45180510	GM19239	blood:	n/a
37	chr17:45177378-45177428	HCF	heart:	n/a
38	chr17:45177429-45177479	HepG2	liver:	n/a
39	chr17:45177378-45177428	ovcar-3	ovarian:	n/a
40	chr17:45177429-45177479	AG09309	skin:	n/a
41	chr17:45177598-45177648	LNCaP	prostate:	n/a
42	chr17:45174155-45174205	HCPEpiC	choroid plexus:	n/a
43	chr17:45177598-45177648	HMEC	breast:	n/a
44	chr17:45177429-45177479	NHDF-neo	bronchial:	n/a
45	chr17:45183984-45184034	HPAEpiC	pulmonary alveolar:	n/a
46	chr17:45180460-45180510	ECC-1	luminal epithelium:	n/a
47	chr17:45177859-45177909	HEK293	kidney:	embryo
48	chr17:45177628-45177678	HRE	kidney:	n/a
49	chr17:45183984-45184034	NH-A	brain:	n/a
50	chr17:45177378-45177428	HIPEpiC	eye:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:45156502..45159050-chr17:45162212..45165184,2	K562	blood:
2	chr17:45159211..45163683-chr17:45163741..45168313,5	K562	blood:
3	chr17:45177573..45179138-chr17:45179846..45181452,2	MCF-7	breast:
4	chr17:45170129..45171669-chr17:45173350..45174934,2	K562	blood:
5	chr17:44302347..44303352-chr17:45177408..45178065,4	HCT-116	colon:
6	chr17:45163760..45166072-chr17:45166357..45168655,2	K562	blood:
7	chr17:45179866..45182150-chr17:45185203..45188192,2	K562	blood:
8	chr17:45162074..45163604-chr17:45171046..45173992,2	MCF-7	breast:
9	chr17:45169541..45171629-chr17:45172586..45174850,2	K562	blood:
10	chr17:45170129..45171669-chr17:45173350..45174934,2	K562	blood:
11	chr17:45143258..45146165-chr17:45178013..45180632,2	K562	blood:
12	chr17:45145658..45148463-chr17:45161187..45163786,2	MCF-7	breast:
13	chr17:45162074..45163604-chr17:45171046..45173992,2	MCF-7	breast:
14	chr17:45155821..45158287-chr17:45163734..45167832,3	K562	blood:
15	chr17:45155821..45158287-chr17:45163734..45167832,3	K562	blood:
16	chr17:45179866..45182150-chr17:45185203..45188192,2	K562	blood:
17	chr17:45190584..45193064-chr17:45401116..45402656,2	K562	blood:
18	chr17:45195494..45197087-chr17:45199093..45201965,2	K562	blood:
19	chr17:45142727..45145152-chr17:45150394..45151973,2	K562	blood:
20	chr17:45156502..45159050-chr17:45162212..45165184,2	K562	blood:
21	chr17:45169541..45171629-chr17:45172586..45174850,2	K562	blood:
22	chr17:45143436..45146346-chr17:45178059..45181405,3	K562	blood:
23	chr17:45159211..45163683-chr17:45163741..45168313,5	K562	blood:
24	chr17:45163760..45166072-chr17:45166357..45168655,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RPRML-3	chr17:45158273-45158298	NONHSAT054279
2	lnc-RPRML-3	chr17:45177201-45177605	ENSG00000262879.1
3	lnc-RPRML-3	chr17:45177201-45177560	NONHSAT054278
4	lnc-RPRML-3	chr17:45177201-45177614	NONHSAT054277
5	lnc-RPRML-3	chr17:45177201-45177614	ENSG00000262879.1
6	lnc-RPRML-3	chr17:45159286-45159716	ENSG00000262879.1
7	lnc-RPRML-3	chr17:45177201-45177631	NONHSAT054279
8	lnc-RPRML-3	chr17:45176744-45177617	NONHSAT054281

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	CDC27	hsa-miR-16-5p	chr17:45195634-45195658
2	CDC27	hsa-miR-16-5p	chr17:45195640-45195634

Variant related genes	Relation type
ENSG00000221016	TF binding region
ENSG00000262879	TF binding region
ENSG00000221016	CpG island
ENSG00000262879	CpG island
ENSG00000120071	chromatin interactions
ENSG00000004897	chromatin interactions
ENSG00000262879	chromatin interactions
ENSG00000178852	chromatin interactions

Extended variants
information (count: 1513 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:1513 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2316667	chr17:45151549-45151550	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs545060968	chr17:45151577-45151578	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs558630758	chr17:45151590-45151591	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs572081815	chr17:45151644-45151645	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs541433487	chr17:45151730-45151731	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs35555199	chr17:45151735-45151736	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs200303166	chr17:45151798-45151799	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs185250911	chr17:45151824-45151825	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs56932442	chr17:45151871-45151872	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs530400689	chr17:45151936-45151937	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs532888926	chr17:45151953-45151954	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs543798205	chr17:45151979-45151980	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs115123426	chr17:45152013-45152014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs143416212	chr17:45152070-45152071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs551471277	chr17:45152179-45152180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs571379236	chr17:45152231-45152232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs527424442	chr17:45152274-45152275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs200198234	chr17:45152275-45152276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs574745147	chr17:45152276-45152277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs74595563	chr17:45152277-45152278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs77996300	chr17:45152285-45152286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs112145885	chr17:45152329-45152330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs113623097	chr17:45152354-45152355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs190799199	chr17:45152393-45152394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs569470996	chr17:45152419-45152420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs12942936	chr17:45152428-45152429	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs148350294	chr17:45152468-45152469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs370825806	chr17:45152508-45152509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs572183514	chr17:45152514-45152515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs200550708	chr17:45152525-45152526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs534837734	chr17:45152648-45152649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs574766724	chr17:45152651-45152652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs554935929	chr17:45152668-45152669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs183396570	chr17:45152677-45152678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs372129554	chr17:45152683-45152684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs544056007	chr17:45152705-45152706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs16941566	chr17:45152745-45152746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs140679333	chr17:45152868-45152869	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs386797409	chr17:45152914-45152915	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs77919729	chr17:45152915-45152916	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
41	rs188827687	chr17:45152948-45152949	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs527371009	chr17:45152975-45152976	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs191722263	chr17:45152983-45152984	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs145683395	chr17:45152994-45152995	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs543542899	chr17:45153011-45153012	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs529666537	chr17:45153052-45153053	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs73985130	chr17:45153088-45153089	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs569633880	chr17:45153135-45153136	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs564784948	chr17:45153145-45153146	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs551935138	chr17:45153152-45153153	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:120)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Melanoma	18172304	CNVD
Moyamoya disease	22323933	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ovarian cancer	21781307	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell lymphomas	19863542	CNVD
Cancer	16751803	CNVD
Chordoma	21602918	CNVD
Neurofibromatosis	20686819	CNVD
Peripheral nerve sheath tumors	20686819	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	17897457	CNVD
Neuroblastoma	17327916	CNVD
Breast cancer	21264507	CNVD
Endometrial cancer	22040021	CNVD
Neuroblastoma	21484798	CNVD
Breast cancer	22028636	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute myeloid leukemia	20724749	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Gastric cancer	17167181	CNVD
Breast cancer	19287154	CNVD
Leukemia	20874852	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Neuroblastoma	18664255	CNVD
Neuroblastoma	17533364	CNVD
Human rectal carcinomas	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Breast cancer	17457667	CNVD
Breast cancer	16951389	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22048815	CNVD
Breast cancer	17603634	CNVD
Follicular lymphoma	20505157	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	20953835	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
TAR Syndrome	17847015	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17850661	CNVD
Breast cancer	19261255	CNVD
Lung cancer	16773561	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Basal-like breast cancer	18066063	CNVD
Breast cancer	20031965	CNVD
Colorectal cancer	19287155	CNVD
Hereditary breast	19566914	CNVD
Ovarian cancer	19047089	CNVD
Ovarian cancer	19566914	CNVD
Triple-negative breast cancer	18950515	CNVD
Breast cancer	16846527	CNVD
Bladder cancer	21909424	CNVD
Chronic lymphocytic leukemia	21546498	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
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	21251322	CNVD
Ewing''s sarcoma	22429812	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Breast cancer	17142309	CNVD
Breast cancer	16397240	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Non-syndromic sensorineural hearing loss	21084979	CNVD
Autism	22817714	CNVD
Breast cancer	20409316	CNVD
Cancer	17160897	CNVD
Frontotemporal lobar degeneration	19640594	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:886 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:45145000-45151600	Weak transcription	Psoas Muscle	Psoas
2	chr17:45145000-45152200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr17:45145000-45152400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr17:45145000-45158800	Weak transcription	NHLF	lung
5	chr17:45145000-45163600	Weak transcription	Aorta	Aorta
6	chr17:45145000-45163800	Weak transcription	Small Intestine	intestine
7	chr17:45145000-45164600	Weak transcription	Brain Angular Gyrus	brain
8	chr17:45145000-45169800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr17:45145000-45169800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr17:45145000-45169800	Weak transcription	Fetal Lung	lung
11	chr17:45145000-45176400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr17:45145000-45176600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr17:45145000-45176800	Weak transcription	Lung	lung
14	chr17:45145200-45157400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr17:45145200-45158800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr17:45145200-45162200	Weak transcription	HepG2	liver
17	chr17:45145200-45169200	Weak transcription	Primary B cells from cord blood	blood
18	chr17:45145200-45170200	Weak transcription	Brain Germinal Matrix	brain
19	chr17:45145200-45176600	Weak transcription	HUES48 Cell Line	embryonic stem cell
20	chr17:45145400-45176000	Weak transcription	Primary T cells from cord blood	blood
21	chr17:45146000-45158600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
22	chr17:45146400-45169800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
23	chr17:45146400-45170800	Weak transcription	Dnd41	blood
24	chr17:45147200-45151800	Enhancers	Primary monocytes fromperipheralblood	blood
25	chr17:45148200-45151800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr17:45148200-45155200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr17:45148600-45162200	Weak transcription	Stomach Mucosa	stomach
28	chr17:45148800-45157400	Weak transcription	A549	lung
29	chr17:45148800-45161200	Weak transcription	Hela-S3	cervix
30	chr17:45148800-45175400	Weak transcription	Rectal Mucosa Donor 29	rectum
31	chr17:45149000-45154800	Weak transcription	HMEC	breast
32	chr17:45149000-45154800	Weak transcription	NHEK	skin
33	chr17:45149000-45164200	Weak transcription	Primary T helper cells fromperipheralblood	blood
34	chr17:45149000-45168600	Weak transcription	Primary B cells from peripheral blood	blood
35	chr17:45149000-45170000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr17:45149000-45173800	Weak transcription	Primary T helper cells PMA-I stimulated	--
37	chr17:45149600-45155800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
38	chr17:45149600-45175400	Weak transcription	Primary T cells fromperipheralblood	blood
39	chr17:45149600-45176800	Weak transcription	Sigmoid Colon	Sigmoid Colon
40	chr17:45150200-45170000	Weak transcription	Ovary	ovary
41	chr17:45150200-45174600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
42	chr17:45150400-45151600	Weak transcription	Fetal Muscle Trunk	muscle
43	chr17:45150400-45152800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr17:45150600-45151600	Enhancers	Primary hematopoietic stem cells short term culture	blood
45	chr17:45150600-45152000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr17:45150600-45152000	Enhancers	Monocytes-CD14+_RO01746	blood
47	chr17:45150600-45152800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr17:45150600-45153400	Weak transcription	Brain Cingulate Gyrus	brain
49	chr17:45150600-45154800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr17:45150600-45154800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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