Variant report

Variant	nsv1311
Chromosome Location	chr14:65352722-65379802
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:65377626-65377826	K562	blood:	n/a	n/a
2	ARID3A	chr14:65358561-65358873	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:65377651-65377906	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:65358532-65358848	K562	blood:	n/a	n/a
5	ATF1	chr14:65366760-65366960	K562	blood:	n/a	n/a
6	ATF1	chr14:65379131-65379330	K562	blood:	n/a	n/a
7	ATF1	chr14:65358514-65358786	K562	blood:	n/a	n/a
8	BRCA1	chr14:65358566-65358821	H1-hESC	embryonic stem cell:	n/a	n/a
9	CBX3	chr14:65360978-65361212	K562	blood:	n/a	n/a
10	CEBPB	chr14:65374623-65374717	K562	blood:	n/a	n/a
11	CEBPB	chr14:65358591-65358854	K562	blood:	n/a	n/a
12	CEBPB	chr14:65357433-65357786	K562	blood:	n/a	n/a
13	CEBPB	chr14:65374473-65374786	A549	lung:	n/a	n/a
14	CEBPB	chr14:65371943-65372179	IMR90	lung:	n/a	n/a
15	CEBPB	chr14:65371920-65372417	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr14:65371966-65372308	HepG2	liver:	n/a	n/a
17	CTCF	chr14:65377709-65377856	Lung_OC	lung:	n/a	chr14:65377772-65377788 chr14:65377766-65377787
18	CTCF	chr14:65377660-65377810	RPTEC	kidney:	n/a	chr14:65377772-65377788 chr14:65377766-65377787
19	CTCF	chr14:65358511-65358938	IMR90	lung:	n/a	chr14:65358690-65358711 chr14:65358528-65358537 chr14:65358697-65358710 chr14:65358695-65358713
20	CTCF	chr14:65377524-65378108	HCT-116	colon:	n/a	chr14:65377772-65377788 chr14:65377766-65377787
21	CTCF	chr14:65377720-65377870	HPAF	blood vessel:	n/a	chr14:65377772-65377788 chr14:65377766-65377787
22	CTCF	chr14:65377697-65377889	LNCaP	prostate:	n/a	chr14:65377772-65377788 chr14:65377766-65377787
23	CTCF	chr14:65377700-65377850	GM12873	blood:	n/a	chr14:65377772-65377788 chr14:65377766-65377787
24	CTCF	chr14:65358686-65358759	A549	lung:	n/a	chr14:65358690-65358711 chr14:65358697-65358710 chr14:65358695-65358713
25	CTCF	chr14:65358595-65358851	MCF-7	breast:	n/a	chr14:65358690-65358711 chr14:65358697-65358710 chr14:65358695-65358713
26	CTCF	chr14:65358680-65358830	SK-N-SH_RA	brain:	n/a	chr14:65358690-65358711 chr14:65358697-65358710 chr14:65358695-65358713
27	CTCF	chr14:65358660-65358810	GM12875	blood:	n/a	chr14:65358690-65358711 chr14:65358697-65358710 chr14:65358695-65358713
28	CTCF	chr14:65358660-65358810	GM12872	blood:	n/a	chr14:65358690-65358711 chr14:65358697-65358710 chr14:65358695-65358713
29	CTCF	chr14:65377700-65377850	SAEC	small airway:	n/a	chr14:65377772-65377788 chr14:65377766-65377787
30	CTCF	chr14:65377686-65377894	Medullo	brain:	n/a	chr14:65377772-65377788 chr14:65377766-65377787
31	CTCF	chr14:65358600-65358750	HMF	breast:	n/a	chr14:65358690-65358711 chr14:65358697-65358710 chr14:65358695-65358713
32	CTCF	chr14:65358561-65358844	Pancreas_OC	pancreas:	n/a	chr14:65358690-65358711 chr14:65358697-65358710 chr14:65358695-65358713
33	CTCF	chr14:65377594-65377980	IMR90	lung:	n/a	chr14:65377772-65377788 chr14:65377766-65377787
34	CTCF	chr14:65358680-65358830	GM12869	blood:	n/a	chr14:65358690-65358711 chr14:65358697-65358710 chr14:65358695-65358713
35	CTCF	chr14:65358700-65358850	RPTEC	kidney:	n/a	n/a
36	CTCF	chr14:65356279-65356332	GM19240	blood:	n/a	n/a
37	CTCF	chr14:65358640-65358790	GM12878	blood:	n/a	chr14:65358690-65358711 chr14:65358697-65358710 chr14:65358695-65358713
38	CTCF	chr14:65377680-65377830	HL-60	blood:	n/a	chr14:65377772-65377788 chr14:65377766-65377787
39	CTCF	chr14:65377960-65378110	SK-N-SH_RA	brain:	n/a	n/a
40	CTCF	chr14:65358596-65358821	LNCaP	prostate:	n/a	chr14:65358690-65358711 chr14:65358697-65358710 chr14:65358695-65358713
41	CTCF	chr14:65358640-65358790	Hela-S3	cervix:	n/a	chr14:65358690-65358711 chr14:65358697-65358710 chr14:65358695-65358713
42	CTCF	chr14:65358482-65358813	A549	lung:	n/a	chr14:65358690-65358711 chr14:65358528-65358537 chr14:65358697-65358710 chr14:65358695-65358713
43	CTCF	chr14:65377700-65377850	GM12875	blood:	n/a	chr14:65377772-65377788 chr14:65377766-65377787
44	CTCF	chr14:65377598-65377934	HepG2	liver:	n/a	chr14:65377772-65377788 chr14:65377766-65377787
45	CTCF	chr14:65358480-65358884	ECC-1	luminal epithelium:	n/a	chr14:65358690-65358711 chr14:65358528-65358537 chr14:65358697-65358710 chr14:65358695-65358713
46	CTCF	chr14:65377720-65377870	HEK293	kidney:	n/a	chr14:65377772-65377788 chr14:65377766-65377787
47	CTCF	chr14:65358660-65358810	AoAF	blood vessel:	n/a	chr14:65358690-65358711 chr14:65358697-65358710 chr14:65358695-65358713
48	CTCF	chr14:65358640-65358790	AG04449	skin:	n/a	chr14:65358690-65358711 chr14:65358697-65358710 chr14:65358695-65358713
49	CTCF	chr14:65358680-65358830	HCM	heart:	n/a	chr14:65358690-65358711 chr14:65358697-65358710 chr14:65358695-65358713
50	CTCF	chr14:65358620-65358770	NB4	blood:	n/a	chr14:65358690-65358711 chr14:65358697-65358710 chr14:65358695-65358713

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:65377797-65377847	HCT-116	colon:	n/a
2	chr14:65377797-65377847	ovcar-3	ovarian:	n/a
3	chr14:65377797-65377847	PrEC	prostate:	n/a
4	chr14:65377797-65377847	NB4	blood:	n/a
5	chr14:65377797-65377847	PANC-1	pancreas:	n/a
6	chr14:65377797-65377847	K562	blood:	n/a
7	chr14:65377797-65377847	HRCEpiC	kidney:	n/a
8	chr14:65377797-65377847	SAEC	small airway:	n/a
9	chr14:65377797-65377847	T-47D	breast:	n/a
10	chr14:65377797-65377847	HCM	heart:	n/a
11	chr14:65377797-65377847	HRPEpiC	eye:	n/a
12	chr14:65377797-65377847	NT2-D1	testis:	n/a
13	chr14:65377797-65377847	HCPEpiC	choroid plexus:	n/a
14	chr14:65377797-65377847	A549	lung:	n/a
15	chr14:65377797-65377847	CMK	blood:	n/a
16	chr14:65377797-65377847	HPAEpiC	pulmonary alveolar:	n/a
17	chr14:65377797-65377847	HCF	heart:	n/a
18	chr14:65377797-65377847	HEK293	kidney:	embryo
19	chr14:65377797-65377847	AG04450	lung:	fetal
20	chr14:65377797-65377847	MCF-7	breast:	n/a
21	chr14:65377797-65377847	SKMC	muscle:	n/a
22	chr14:65377797-65377847	GM12878	blood:	n/a
23	chr14:65377797-65377847	AG10803	skin:	n/a
24	chr14:65377797-65377847	HUVEC	blood vessel:	n/a
25	chr14:65377797-65377847	AoSMC	blood vessel:	n/a
26	chr14:65377797-65377847	HepG2	liver:	n/a
27	chr14:65377797-65377847	SK-N-SH_RA	brain:	n/a
28	chr14:65377797-65377847	SK-N-SH	brain:	n/a
29	chr14:65377797-65377847	RPTEC	kidney:	n/a
30	chr14:65377797-65377847	SK-N-MC	brain:	n/a
31	chr14:65377797-65377847	BJ	skin:	n/a
32	chr14:65377797-65377847	HNPCEpiC	eye:	n/a
33	chr14:65377797-65377847	H1-hESC	embryonic stem cell:	embryo
34	chr14:65377797-65377847	MCF10A-Er-Src	breast:	n/a
35	chr14:65377797-65377847	HL-60	blood:	n/a
36	chr14:65377797-65377847	GM19239	blood:	n/a
37	chr14:65377797-65377847	LNCaP	prostate:	n/a
38	chr14:65377797-65377847	GM12892	blood:	n/a
39	chr14:65377797-65377847	Hepatocyte	liver:	n/a
40	chr14:65377797-65377847	HMEC	breast:	n/a
41	chr14:65377797-65377847	BE2_C	brain:	n/a
42	chr14:65377797-65377847	AG09309	skin:	n/a
43	chr14:65377797-65377847	AG04449	skin:	fetal
44	chr14:65377797-65377847	GM06990	blood:	n/a
45	chr14:65377797-65377847	Jurkat	blood:	n/a
46	chr14:65377797-65377847	HRE	kidney:	n/a
47	chr14:65377797-65377847	ProgFib	skin:	n/a
48	chr14:65377797-65377847	NHDF-neo	bronchial:	n/a
49	chr14:65377797-65377847	HAEpiC	amniotic membrane:	n/a
50	chr14:65377797-65377847	Caco-2	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:65268216..65269184-chr14:65358330..65359038,4	K562	blood:
2	chr14:65264248..65268196-chr14:65377647..65381035,3	MCF-7	breast:
3	chr14:65379731..65383710-chr14:65424558..65427647,5	MCF-7	breast:
4	chr14:65373381..65376070-chr14:65381167..65383917,2	MCF-7	breast:
5	chr14:65356440..65358700-chr14:65379769..65381546,2	MCF-7	breast:
6	chr14:65289223..65290628-chr14:65357779..65359171,7	MCF-7	breast:
7	chr14:65346776..65351606-chr14:65355142..65358604,5	K562	blood:
8	chr14:65373180..65376214-chr14:65389660..65391976,3	K562	blood:
9	chr14:65352038..65354745-chr14:65354823..65356401,2	MCF-7	breast:
10	chr14:65238323..65239708-chr14:65358202..65359292,7	MCF-7	breast:
11	chr14:65370140..65372301-chr14:65378227..65382281,3	K562	blood:
12	chr14:65376372..65378588-chr14:65381042..65383849,2	K562	blood:
13	chr14:65289311..65290700-chr14:65357720..65359432,13	MCF-7	breast:
14	chr14:65289524..65290526-chr14:65358021..65359324,8	K562	blood:
15	chr14:65373753..65376214-chr14:65389660..65391976,2	K562	blood:
16	chr14:65238831..65239785-chr14:65358174..65359063,5	MCF-7	breast:
17	chr14:65267486..65269217-chr14:65357718..65359262,14	MCF-7	breast:
18	chr14:65374078..65375852-chr14:65379267..65381463,2	K562	blood:
19	chr14:65288738..65289433-chr14:65358177..65359166,2	K562	blood:
20	chr14:65353028..65355615-chr14:65356230..65358479,2	K562	blood:
21	chr14:65352038..65354745-chr14:65354823..65356401,2	MCF-7	breast:
22	chr14:65345386..65349759-chr14:65351524..65353392,4	K562	blood:
23	chr14:65371374..65373964-chr14:65403837..65405514,2	MCF-7	breast:
24	chr14:65346776..65348701-chr14:65353935..65356642,2	K562	blood:
25	chr14:65377652..65378279-chr14:65486390..65487336,2	K562	blood:
26	chr14:65348790..65350431-chr14:65354334..65355956,2	K562	blood:
27	chr14:65376890..65379070-chr14:65449089..65451973,3	MCF-7	breast:
28	chr14:65263268..65264769-chr14:65377543..65379077,2	K562	blood:
29	chr14:65360076..65361766-chr14:65362287..65363875,2	MCF-7	breast:
30	chr14:65264347..65266634-chr14:65358841..65360422,2	MCF-7	breast:
31	chr14:65368343..65372150-chr14:65374320..65377224,3	K562	blood:
32	chr14:65290012..65290932-chr14:65377431..65378083,2	MCF-7	breast:
33	chr14:65306477..65308569-chr14:65377752..65379840,2	MCF-7	breast:
34	chr14:65358336..65361161-chr14:65365213..65366947,2	K562	blood:
35	chr14:65360076..65361766-chr14:65362287..65363875,2	MCF-7	breast:
36	chr14:65346800..65348898-chr14:65351625..65354536,2	K562	blood:
37	chr14:65353028..65355615-chr14:65356230..65358479,2	K562	blood:
38	chr14:65347011..65349276-chr14:65350145..65352997,3	MCF-7	breast:
39	chr14:65377331..65378166-chr14:65449998..65450968,5	MCF-7	breast:
40	chr14:65376789..65378335-chr14:65383134..65384665,2	MCF-7	breast:
41	chr14:65358336..65361161-chr14:65365213..65366947,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPX2-3	chr14:65376206-65376498	NONHSAT037356

Variant related genes	Relation type
CHURC1-FNTB	TF binding region
RPPH1-2P	TF binding region
CHURC1	TF binding region
FNTB	TF binding region
CHURC1-FNTB	CpG island
RPPH1-2P	CpG island
CHURC1	CpG island
FNTB	CpG island
ENSG00000139998	chromatin interactions
ENSG00000070182	chromatin interactions
ENSG00000252497	chromatin interactions
ENSG00000258289	chromatin interactions
ENSG00000125954	chromatin interactions

Extended variants
information (count: 959 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:959 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544311162	chr14:65352758-65352759	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs202222395	chr14:65352773-65352774	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs1957432	chr14:65352796-65352797	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs368421842	chr14:65352847-65352848	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs72726265	chr14:65352887-65352888	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs540193229	chr14:65352936-65352937	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs566008320	chr14:65352969-65352970	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs8019346	chr14:65353011-65353012	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs529106131	chr14:65353097-65353098	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs542461175	chr14:65353099-65353100	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs369300411	chr14:65353141-65353142	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs1957431	chr14:65353187-65353188	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs530939474	chr14:65353215-65353216	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs72726266	chr14:65353242-65353243	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs114605867	chr14:65353256-65353257	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs533179113	chr14:65353257-65353258	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs546924093	chr14:65353307-65353308	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs186779720	chr14:65353360-65353361	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs117552608	chr14:65353380-65353381	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs556032836	chr14:65353404-65353405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs569453794	chr14:65353409-65353410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs538409102	chr14:65353444-65353445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs373497631	chr14:65353500-65353501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs1957430	chr14:65353506-65353507	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs191236497	chr14:65353627-65353628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs1998333	chr14:65353632-65353633	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs182331019	chr14:65353634-65353635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs553727217	chr14:65353756-65353757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs573640697	chr14:65353758-65353759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs8021599	chr14:65353772-65353773	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs562413147	chr14:65353774-65353775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs187754224	chr14:65353796-65353797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs73279839	chr14:65353834-65353835	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs560961207	chr14:65353907-65353908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs564424780	chr14:65353949-65353950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs538010897	chr14:65353973-65353974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs546716342	chr14:65354009-65354010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs566858816	chr14:65354011-65354012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs534926792	chr14:65354026-65354027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs542322494	chr14:65354027-65354028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs561997558	chr14:65354028-65354029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs1957429	chr14:65354033-65354034	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs193117869	chr14:65354041-65354042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs1957428	chr14:65354058-65354059	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs1957427	chr14:65354085-65354086	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs150270296	chr14:65354102-65354103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs533877626	chr14:65354122-65354123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs185186929	chr14:65354151-65354152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs375196746	chr14:65354165-65354166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs573321769	chr14:65354225-65354226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17603634	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Barrett''s syndrome	19417022	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	17440070	CNVD
early-passage human iPS cells	21368824	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:67 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:65352200-65353400	Enhancers	K562	blood
2	chr14:65353200-65353400	Enhancers	Gastric	stomach
3	chr14:65353400-65357400	Weak transcription	K562	blood
4	chr14:65357400-65358600	Enhancers	K562	blood
5	chr14:65357800-65358400	Enhancers	Liver	Liver
6	chr14:65357800-65358600	Enhancers	Skeletal Muscle Female	skeletal muscle
7	chr14:65358000-65358600	Enhancers	Skeletal Muscle Male	skeletal muscle
8	chr14:65358200-65359000	Enhancers	Pancreatic Islets	Pancreatic Islet
9	chr14:65358400-65358600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr14:65358600-65368000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr14:65364200-65364800	Enhancers	Thymus	Thymus
12	chr14:65364400-65364800	Bivalent Enhancer	Fetal Thymus	thymus
13	chr14:65366600-65367000	Enhancers	K562	blood
14	chr14:65372000-65373200	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr14:65372000-65373400	Enhancers	Monocytes-CD14+_RO01746	blood
16	chr14:65372200-65373000	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr14:65372200-65373200	Enhancers	Primary neutrophils fromperipheralblood	blood
18	chr14:65372400-65373200	Enhancers	HMEC	breast
19	chr14:65372400-65373800	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr14:65372400-65373800	Enhancers	Hela-S3	cervix
21	chr14:65372400-65374000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr14:65372600-65373000	Enhancers	Primary hematopoietic stem cells	blood
23	chr14:65372600-65373200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr14:65372600-65373400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr14:65372600-65373800	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr14:65372800-65373000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
27	chr14:65372800-65373200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr14:65373200-65376000	Weak transcription	Primary monocytes fromperipheralblood	blood
29	chr14:65373800-65374400	Weak transcription	Hela-S3	cervix
30	chr14:65373800-65379000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
31	chr14:65374000-65379200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr14:65376200-65376400	Enhancers	Primary monocytes fromperipheralblood	blood
33	chr14:65378000-65378200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
34	chr14:65378200-65380600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr14:65379000-65379200	Enhancers	GM12878-XiMat	blood
36	chr14:65379000-65379600	Enhancers	Primary T cells from cord blood	blood
37	chr14:65379000-65379800	Enhancers	Brain Anterior Caudate	brain
38	chr14:65379000-65380600	Enhancers	Primary hematopoietic stem cells short term culture	blood
39	chr14:65379000-65380600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr14:65379200-65379600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
41	chr14:65379200-65379600	Bivalent Enhancer	NH-A	brain
42	chr14:65379200-65379800	Enhancers	K562	blood
43	chr14:65379200-65380000	Enhancers	Primary T helper cells fromperipheralblood	blood
44	chr14:65379200-65380000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr14:65379400-65379600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
46	chr14:65379400-65379600	Enhancers	Duodenum Mucosa	Duodenum
47	chr14:65379400-65379800	Enhancers	Brain Cingulate Gyrus	brain
48	chr14:65379400-65379800	Enhancers	Brain Substantia Nigra	brain
49	chr14:65379400-65380000	Enhancers	Primary hematopoietic stem cells	blood
50	chr14:65379400-65380600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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