Variant report

Variant	nsv873887
Chromosome Location	chr2:39468676-39601889
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:615)
CpG islands
(count:610)
Chromatin interactive
region (count:58)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:615 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:39565636-39565931	K562	blood:	n/a	n/a
2	ARID3A	chr2:39475252-39475385	HepG2	liver:	n/a	n/a
3	ATF2	chr2:39592014-39592651	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr2:39493258-39493611	GM12878	blood:	n/a	chr2:39493418-39493429
5	BCL11A	chr2:39592276-39592551	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr2:39492072-39492073	GM12878	blood:	n/a	n/a
7	CBX3	chr2:39586548-39587042	HCT-116	colon:	n/a	n/a
8	CBX3	chr2:39587459-39587917	K562	blood:	n/a	n/a
9	CBX3	chr2:39586345-39587251	K562	blood:	n/a	n/a
10	CBX3	chr2:39589717-39590155	HCT-116	colon:	n/a	n/a
11	CBX3	chr2:39587491-39587917	K562	blood:	n/a	n/a
12	CBX3	chr2:39586565-39587203	K562	blood:	n/a	n/a
13	CCNT2	chr2:39598280-39598370	K562	blood:	n/a	n/a
14	CCNT2	chr2:39525801-39525966	K562	blood:	n/a	n/a
15	CEBPB	chr2:39540873-39541107	IMR90	lung:	n/a	n/a
16	CEBPB	chr2:39531887-39532429	HepG2	liver:	n/a	n/a
17	CEBPB	chr2:39565527-39565883	K562	blood:	n/a	n/a
18	CEBPB	chr2:39536643-39536825	A549	lung:	n/a	n/a
19	CEBPB	chr2:39493515-39493518	A549	lung:	n/a	n/a
20	CEBPB	chr2:39597373-39597648	IMR90	lung:	n/a	n/a
21	CEBPB	chr2:39531891-39532296	IMR90	lung:	n/a	n/a
22	CEBPB	chr2:39531927-39532215	K562	blood:	n/a	n/a
23	CEBPB	chr2:39592328-39592697	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr2:39531899-39532359	A549	lung:	n/a	n/a
25	CEBPB	chr2:39536641-39536800	K562	blood:	n/a	n/a
26	CEBPB	chr2:39567654-39567912	HepG2	liver:	n/a	chr2:39567784-39567795
27	CEBPB	chr2:39531907-39532278	MCF-7	breast:	n/a	n/a
28	CEBPB	chr2:39523390-39523652	HepG2	liver:	n/a	n/a
29	CEBPB	chr2:39523389-39523635	IMR90	lung:	n/a	n/a
30	CEBPB	chr2:39580016-39580199	A549	lung:	n/a	n/a
31	CEBPB	chr2:39590860-39590903	HepG2	liver:	n/a	chr2:39590878-39590889
32	CEBPB	chr2:39531884-39532253	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr2:39567618-39567844	A549	lung:	n/a	chr2:39567784-39567795
34	CEBPB	chr2:39536610-39536879	IMR90	lung:	n/a	n/a
35	CEBPD	chr2:39565641-39566115	K562	blood:	n/a	n/a
36	CEBPD	chr2:39565590-39566071	K562	blood:	n/a	n/a
37	CHD1	chr2:39504205-39504287	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD1	chr2:39492022-39492064	GM12878	blood:	n/a	n/a
39	CHD2	chr2:39592273-39592532	H1-hESC	embryonic stem cell:	n/a	n/a
40	CREB1	chr2:39592236-39592584	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr2:39553920-39554070	BJ	skin:	n/a	n/a
42	CTCF	chr2:39475227-39475320	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr2:39553960-39554110	HCT-116	colon:	n/a	n/a
44	CTCF	chr2:39553931-39554055	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr2:39513395-39513490	MCF-7	breast:	n/a	n/a
46	CTCF	chr2:39553960-39554110	GM12872	blood:	n/a	n/a
47	CTCF	chr2:39513342-39513483	MCF-7	breast:	n/a	n/a
48	CTCF	chr2:39495001-39495050	K562	blood:	n/a	n/a
49	CTCF	chr2:39472300-39472450	GM12873	blood:	n/a	n/a
50	CTCF	chr2:39596140-39596290	HEEpiC	esophagus:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:39470725-39470775	NT2-D1	testis:	n/a
2	chr2:39470750-39470800	A549	lung:	n/a
3	chr2:39493603-39493653	HCT-116	colon:	n/a
4	chr2:39471182-39471232	SK-N-SH	brain:	n/a
5	chr2:39470725-39470775	HEK293	kidney:	embryo
6	chr2:39597028-39597078	HL-60	blood:	n/a
7	chr2:39471028-39471078	SK-N-SH	brain:	n/a
8	chr2:39475086-39475136	SK-N-SH_RA	brain:	n/a
9	chr2:39472684-39472734	A549	lung:	n/a
10	chr2:39470750-39470800	RPTEC	kidney:	n/a
11	chr2:39470743-39470793	AG04450	lung:	fetal
12	chr2:39471182-39471232	BE2_C	brain:	n/a
13	chr2:39471028-39471078	NB4	blood:	n/a
14	chr2:39471182-39471232	HNPCEpiC	eye:	n/a
15	chr2:39470743-39470793	AoSMC	blood vessel:	n/a
16	chr2:39597028-39597078	NB4	blood:	n/a
17	chr2:39475086-39475136	IMR90	lung:	fetal
18	chr2:39472197-39472247	Jurkat	blood:	n/a
19	chr2:39493603-39493653	HL-60	blood:	n/a
20	chr2:39597028-39597078	NH-A	brain:	n/a
21	chr2:39597028-39597078	SK-N-SH	brain:	n/a
22	chr2:39470725-39470775	HCM	heart:	n/a
23	chr2:39472197-39472247	HCPEpiC	choroid plexus:	n/a
24	chr2:39475086-39475136	PANC-1	pancreas:	n/a
25	chr2:39470725-39470775	GM06990	blood:	n/a
26	chr2:39470743-39470793	SK-N-SH_RA	brain:	n/a
27	chr2:39470743-39470793	LNCaP	prostate:	n/a
28	chr2:39472197-39472247	HCT-116	colon:	n/a
29	chr2:39470750-39470800	NB4	blood:	n/a
30	chr2:39471182-39471232	RPTEC	kidney:	n/a
31	chr2:39597028-39597078	AG09319	gingival:	n/a
32	chr2:39472197-39472247	AG09309	skin:	n/a
33	chr2:39475086-39475136	HMEC	breast:	n/a
34	chr2:39475086-39475136	K562	blood:	n/a
35	chr2:39470743-39470793	HUVEC	blood vessel:	n/a
36	chr2:39493603-39493653	NT2-D1	testis:	n/a
37	chr2:39472684-39472734	GM19239	blood:	n/a
38	chr2:39597028-39597078	K562	blood:	n/a
39	chr2:39470750-39470800	GM12892	blood:	n/a
40	chr2:39471182-39471232	HIPEpiC	eye:	n/a
41	chr2:39471182-39471232	SKMC	muscle:	n/a
42	chr2:39470743-39470793	HRE	kidney:	n/a
43	chr2:39472197-39472247	Hela-S3	cervix:	n/a
44	chr2:39475086-39475136	NHDF-neo	bronchial:	n/a
45	chr2:39470750-39470800	HepG2	liver:	n/a
46	chr2:39470725-39470775	Caco-2	colon:	n/a
47	chr2:39475086-39475136	ECC-1	luminal epithelium:	n/a
48	chr2:39470725-39470775	Hepatocyte	liver:	n/a
49	chr2:39597028-39597078	NHDF-neo	bronchial:	n/a
50	chr2:39472197-39472247	HRE	kidney:	n/a

(count:58 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:39556058..39558190-chr2:39561076..39562731,2	MCF-7	breast:
2	chr2:39575333..39576889-chr2:39590648..39593621,2	K562	blood:
3	chr2:39468106..39472763-chr2:39473661..39477001,5	MCF-7	breast:
4	chr2:39484279..39485806-chr2:39491363..39493420,2	MCF-7	breast:
5	chr2:39499119..39502094-chr2:39503052..39505530,2	K562	blood:
6	chr2:39483897..39486099-chr2:39504200..39506352,2	K562	blood:
7	chr2:39578352..39581305-chr2:39581449..39583295,2	MCF-7	breast:
8	chr2:39575333..39576889-chr2:39590648..39593621,2	K562	blood:
9	chr2:39496358..39498173-chr2:39503458..39507219,3	K562	blood:
10	chr2:39560253..39562366-chr2:39574869..39577046,2	K562	blood:
11	chr2:39596692..39599194-chr2:39603552..39605779,2	K562	blood:
12	chr2:39581524..39583959-chr2:39586784..39588300,2	MCF-7	breast:
13	chr2:39554819..39557461-chr2:39561282..39564126,2	K562	blood:
14	chr2:39560253..39562366-chr2:39574869..39577046,2	K562	blood:
15	chr2:39601552..39609752-chr2:39662569..39667062,10	MCF-7	breast:
16	chr2:39476355..39478295-chr2:39480403..39482715,2	MCF-7	breast:
17	chr2:39564092..39565886-chr2:39568968..39572461,3	K562	blood:
18	chr2:39508670..39510493-chr2:39518099..39520672,2	K562	blood:
19	chr2:39476438..39480963-chr2:39481034..39484561,4	K562	blood:
20	chr2:39540552..39542645-chr2:39544069..39547445,3	K562	blood:
21	chr2:39554819..39557461-chr2:39561282..39564126,2	K562	blood:
22	chr2:39556941..39559571-chr2:39560724..39563297,3	K562	blood:
23	chr2:39498139..39500783-chr2:39514401..39516226,2	K562	blood:
24	chr2:39531304..39535719-chr2:39536825..39539603,4	K562	blood:
25	chr2:39490995..39493794-chr2:39495082..39499421,5	K562	blood:
26	chr2:39592431..39595037-chr2:39606994..39609633,2	MCF-7	breast:
27	chr2:39460764..39463142-chr2:39468024..39469641,2	K562	blood:
28	chr2:39508670..39510493-chr2:39518099..39520672,2	K562	blood:
29	chr2:39539961..39541586-chr2:39667193..39669640,2	K562	blood:
30	chr2:39556941..39559571-chr2:39560724..39563297,3	K562	blood:
31	chr2:39489136..39490655-chr2:39494210..39497075,2	K562	blood:
32	chr2:39524953..39527718-chr4:1713296..1715250,2	MCF-7	breast:
33	chr2:39558231..39561041-chr2:39565339..39568222,3	MCF-7	breast:
34	chr2:39490995..39493794-chr2:39495082..39499421,5	K562	blood:
35	chr2:39581524..39583959-chr2:39586784..39588300,2	MCF-7	breast:
36	chr2:39499119..39502094-chr2:39503052..39505530,2	K562	blood:
37	chr2:39531304..39535719-chr2:39536825..39539603,4	K562	blood:
38	chr2:39564092..39565886-chr2:39568968..39572461,3	K562	blood:
39	chr2:39506271..39508619-chr2:39510238..39511844,2	K562	blood:
40	chr2:39569119..39570627-chr2:39583431..39586281,2	K562	blood:
41	chr2:39468106..39472763-chr2:39473661..39477001,5	MCF-7	breast:
42	chr2:39576198..39578818-chr2:39661442..39663917,2	K562	blood:
43	chr17:73408437..73408956-chr2:39475634..39476134,2	MCF-7	breast:
44	chr2:39556058..39558190-chr2:39561076..39562731,2	MCF-7	breast:
45	chr2:39548716..39551632-chr2:39563065..39564786,2	MCF-7	breast:
46	chr2:39476438..39480963-chr2:39481034..39484561,4	K562	blood:
47	chr2:39569119..39570627-chr2:39583431..39586281,2	K562	blood:
48	chr2:39540552..39542645-chr2:39544069..39547445,3	K562	blood:
49	chr2:39554923..39556541-chr2:39556726..39558880,2	MCF-7	breast:
50	chr2:39554923..39556541-chr2:39556726..39558880,2	MCF-7	breast:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM178-4	chr2:39534484-39534610	l_1814_chr2:39518006-39558253_76bGuttman_hLF
2	lnc-TMEM178-4	chr2:39518007-39518182	l_1814_chr2:39518006-39558253_76bGuttman_hLF
3	lnc-CDKL4-3	chr2:39511169-39511421	expReg_chr2_3022_-
4	lnc-CDKL4-6	chr2:39550469-39550945	ENSG00000273035.1
5	lnc-TMEM178-4	chr2:39597056-39597186	l_1814_chr2:39518006-39558253_76bGuttman_hLF
6	lnc-TMEM178-4	chr2:39555172-39558253	l_1814_chr2:39518006-39558253_76bGuttman_hLF
7	lnc-MAP4K3-1	chr2:39473220-39473335	NONHSAT070223
8	lnc-TMEM178-4	chr2:39599228-39599355	l_1814_chr2:39518006-39558253_76bGuttman_hLF
9	lnc-TMEM178-4	chr2:39597776-39597797	l_1814_chr2:39518006-39558253_76bGuttman_hLF
10	lnc-MAP4K3-1	chr2:39472055-39472707	NONHSAT070223
11	lnc-TMEM178-4	chr2:39534902-39535010	l_1814_chr2:39518006-39558253_76bGuttman_hLF

No data

Variant related genes	Relation type
MAP4K3	TF binding region
ENSG00000273035	TF binding region
ENSG00000252473	TF binding region
MAP4K3	CpG island
ENSG00000273035	CpG island
ENSG00000252473	CpG island
ENSG00000273035	chromatin interactions
ENSG00000011566	chromatin interactions
ENSG00000163950	chromatin interactions
ENSG00000270195	chromatin interactions
ENSG00000252473	chromatin interactions
ENSG00000231312	chromatin interactions

Extended variants
information (count: 5589 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:5589 , 50 per page) page: 1 2 3 4 5 6 7 ... 112

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4516411	chr2:39468676-39468677	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs374475724	chr2:39468705-39468706	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs191860689	chr2:39468710-39468711	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs542268719	chr2:39468713-39468714	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs554154731	chr2:39468721-39468722	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs184412759	chr2:39468728-39468729	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs11900474	chr2:39468760-39468761	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs142862664	chr2:39468791-39468792	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs531798358	chr2:39468836-39468837	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs188422056	chr2:39468839-39468840	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs193205187	chr2:39468840-39468841	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs528837702	chr2:39468865-39468866	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs547406346	chr2:39468888-39468889	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs565558677	chr2:39468908-39468909	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs145078116	chr2:39468962-39468963	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs537362300	chr2:39468981-39468982	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs539917660	chr2:39469072-39469073	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs111760328	chr2:39469102-39469103	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs185536552	chr2:39469128-39469129	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs537286987	chr2:39469147-39469148	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs550273601	chr2:39469149-39469150	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs370246608	chr2:39469160-39469161	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs373750797	chr2:39469167-39469168	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs74579526	chr2:39469199-39469200	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs554106981	chr2:39469200-39469201	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs558317629	chr2:39469206-39469207	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs138666548	chr2:39469218-39469219	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs540086502	chr2:39469255-39469256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs558208252	chr2:39469283-39469284	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs576227321	chr2:39469314-39469315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs78333931	chr2:39469398-39469399	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs116154416	chr2:39469447-39469448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs190786014	chr2:39469473-39469474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs566867347	chr2:39469519-39469520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs573370426	chr2:39469520-39469521	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs540792807	chr2:39469599-39469600	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs180797523	chr2:39469679-39469680	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs115212443	chr2:39469698-39469699	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs551648486	chr2:39469715-39469716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs116749806	chr2:39469727-39469728	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs114058533	chr2:39469732-39469733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs373665626	chr2:39469745-39469746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs567490559	chr2:39469767-39469768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs141777478	chr2:39469782-39469783	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs150788912	chr2:39469814-39469815	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs13412798	chr2:39469819-39469820	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs566056305	chr2:39469847-39469848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs113266533	chr2:39469884-39469885	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs79000758	chr2:39469943-39469944	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs576363844	chr2:39470007-39470008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Bladder cancer	21909424	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Non-small cell lung cancer	18927303	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Neurocytoma	17123091	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:3180 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:39423400-39470800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr2:39449200-39477600	Weak transcription	HSMMtube	muscle
3	chr2:39455400-39470600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr2:39455800-39472200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr2:39456000-39472000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr2:39456200-39475600	Weak transcription	NHDF-Ad	bronchial
7	chr2:39460800-39468800	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr2:39464400-39474600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr2:39466800-39470800	Weak transcription	Osteobl	bone
10	chr2:39468000-39469200	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr2:39468000-39469200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
12	chr2:39468200-39469200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr2:39468200-39469200	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr2:39468200-39470200	Enhancers	HepG2	liver
15	chr2:39468400-39469200	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr2:39468400-39469200	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr2:39468400-39469200	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr2:39468400-39469600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr2:39468400-39470600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr2:39468600-39469200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr2:39468600-39469600	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr2:39468600-39469600	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr2:39468600-39469600	Enhancers	HUVEC	blood vessel
24	chr2:39468800-39469000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr2:39468800-39469000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr2:39468800-39469000	Enhancers	Fetal Heart	heart
27	chr2:39468800-39469400	Enhancers	H1 Cell Line	embryonic stem cell
28	chr2:39468800-39469400	Enhancers	H9 Cell Line	embryonic stem cell
29	chr2:39469000-39474000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr2:39469000-39475800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr2:39469200-39469400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr2:39469200-39469400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr2:39469200-39469400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr2:39469200-39469400	Enhancers	Esophagus	oesophagus
35	chr2:39469200-39469400	Enhancers	Lung	lung
36	chr2:39469200-39469600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
37	chr2:39469200-39469600	Enhancers	Left Ventricle	heart
38	chr2:39469200-39470600	Weak transcription	HUES64 Cell Line	embryonic stem cell
39	chr2:39469200-39473600	Weak transcription	Fetal Heart	heart
40	chr2:39469200-39474800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr2:39469200-39475800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr2:39469200-39476400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
43	chr2:39469200-39477400	Weak transcription	HUES48 Cell Line	embryonic stem cell
44	chr2:39469200-39478000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr2:39469200-39503800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr2:39469400-39470000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr2:39469400-39470600	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr2:39469400-39470600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr2:39469400-39470800	Weak transcription	Esophagus	oesophagus
50	chr2:39469400-39471000	Weak transcription	Lung	lung

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