Variant report

Variant	nsv829858
Chromosome Location	chr4:10300236-10492716
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1413)
CpG islands
(count:2139)
Chromatin interactive
region (count:217)
LncRNA
region (count:23)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1413 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:10459741-10459919	K562	blood:	n/a	n/a
2	ARID3A	chr4:10460913-10461399	K562	blood:	n/a	n/a
3	ARID3A	chr4:10405152-10405708	K562	blood:	n/a	n/a
4	ARID3A	chr4:10416844-10416961	K562	blood:	n/a	n/a
5	ARID3A	chr4:10327415-10328296	K562	blood:	n/a	n/a
6	ARID3A	chr4:10373102-10373103	HepG2	liver:	n/a	n/a
7	ATF1	chr4:10327430-10328176	K562	blood:	n/a	n/a
8	ATF3	chr4:10462880-10463147	K562	blood:	n/a	n/a
9	BACH1	chr4:10461300-10461416	K562	blood:	n/a	n/a
10	BACH1	chr4:10444197-10445521	K562	blood:	n/a	n/a
11	BACH1	chr4:10458630-10459108	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr4:10462826-10463788	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr4:10462736-10463370	K562	blood:	n/a	n/a
14	BACH1	chr4:10306752-10306755	K562	blood:	n/a	n/a
15	BACH1	chr4:10446374-10446389	K562	blood:	n/a	n/a
16	BATF	chr4:10461948-10462177	GM12878	blood:	n/a	n/a
17	BATF	chr4:10440575-10440842	GM12878	blood:	n/a	chr4:10440756-10440766
18	BHLHE40	chr4:10459217-10460106	K562	blood:	n/a	n/a
19	BHLHE40	chr4:10405415-10405586	K562	blood:	n/a	n/a
20	BHLHE40	chr4:10462903-10463146	GM12878	blood:	n/a	chr4:10462953-10462969 chr4:10462950-10462966 chr4:10462947-10462963 chr4:10462949-10462965
21	BHLHE40	chr4:10376277-10376477	K562	blood:	n/a	n/a
22	BHLHE40	chr4:10458951-10459247	GM12878	blood:	n/a	chr4:10459125-10459141
23	BHLHE40	chr4:10462844-10463255	K562	blood:	n/a	chr4:10462953-10462969 chr4:10462950-10462966 chr4:10462947-10462963 chr4:10462949-10462965 chr4:10463133-10463149
24	BHLHE40	chr4:10460967-10461712	K562	blood:	n/a	n/a
25	BHLHE40	chr4:10418648-10418697	GM12878	blood:	n/a	n/a
26	BHLHE40	chr4:10458017-10458645	GM12878	blood:	n/a	n/a
27	BHLHE40	chr4:10387822-10388106	K562	blood:	n/a	n/a
28	BHLHE40	chr4:10353695-10353726	K562	blood:	n/a	n/a
29	BRCA1	chr4:10462928-10463022	GM12878	blood:	n/a	n/a
30	BRCA1	chr4:10463085-10463106	HepG2	liver:	n/a	n/a
31	CBX3	chr4:10327581-10328053	K562	blood:	n/a	n/a
32	CBX3	chr4:10458207-10458558	K562	blood:	n/a	n/a
33	CBX3	chr4:10444650-10444918	K562	blood:	n/a	n/a
34	CBX3	chr4:10462629-10463372	K562	blood:	n/a	n/a
35	CBX3	chr4:10327059-10328067	K562	blood:	n/a	n/a
36	CBX3	chr4:10462293-10463603	K562	blood:	n/a	n/a
37	CBX3	chr4:10459827-10460193	K562	blood:	n/a	n/a
38	CCNT2	chr4:10419643-10419843	K562	blood:	n/a	n/a
39	CCNT2	chr4:10327270-10328296	K562	blood:	n/a	n/a
40	CCNT2	chr4:10405344-10405663	K562	blood:	n/a	n/a
41	CCNT2	chr4:10458055-10459262	K562	blood:	n/a	chr4:10458645-10458654 chr4:10458501-10458510 chr4:10458704-10458713
42	CCNT2	chr4:10459488-10460006	K562	blood:	n/a	chr4:10459969-10459978
43	CCNT2	chr4:10346894-10347462	K562	blood:	n/a	n/a
44	CCNT2	chr4:10387632-10388049	K562	blood:	n/a	n/a
45	CCNT2	chr4:10368408-10368665	K562	blood:	n/a	n/a
46	CCNT2	chr4:10323672-10323734	K562	blood:	n/a	n/a
47	CCNT2	chr4:10462773-10463268	K562	blood:	n/a	n/a
48	CEBPB	chr4:10310964-10311220	K562	blood:	n/a	chr4:10311067-10311078
49	CEBPB	chr4:10412857-10413050	K562	blood:	n/a	n/a
50	CEBPB	chr4:10326099-10326299	HepG2	liver:	n/a	chr4:10326229-10326240 chr4:10326226-10326243

(count:2139 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:10460237-10460287	PANC-1	pancreas:	n/a
2	chr4:10447440-10447490	NHBE	bronchial:	n/a
3	chr4:10447440-10447490	AG09319	gingival:	n/a
4	chr4:10459228-10459278	AG09319	gingival:	n/a
5	chr4:10460237-10460287	PANC-1	pancreas:	n/a
6	chr4:10447440-10447490	NHBE	bronchial:	n/a
7	chr4:10447440-10447490	AG09319	gingival:	n/a
8	chr4:10459228-10459278	AG09319	gingival:	n/a
9	chr4:10459836-10459886	LNCaP	prostate:	n/a
10	chr4:10463256-10463306	Hepatocyte	liver:	n/a
11	chr4:10459352-10459402	U87	brain:	n/a
12	chr4:10463620-10463670	HEEpiC	esophagus:	n/a
13	chr4:10462849-10462899	ECC-1	luminal epithelium:	n/a
14	chr4:10443264-10443314	CMK	blood:	n/a
15	chr4:10405694-10405744	SK-N-MC	brain:	n/a
16	chr4:10372870-10372920	HepG2	liver:	n/a
17	chr4:10463590-10463640	HUVEC	blood vessel:	n/a
18	chr4:10372870-10372920	BE2_C	brain:	n/a
19	chr4:10458918-10458968	HL-60	blood:	n/a
20	chr4:10458049-10458099	RPTEC	kidney:	n/a
21	chr4:10459128-10459178	HRE	kidney:	n/a
22	chr4:10458918-10458968	NT2-D1	testis:	n/a
23	chr4:10459435-10459485	RPTEC	kidney:	n/a
24	chr4:10458049-10458099	AG10803	skin:	n/a
25	chr4:10462903-10462953	AoSMC	blood vessel:	n/a
26	chr4:10460237-10460287	HEK293	kidney:	embryo
27	chr4:10459132-10459182	HIPEpiC	eye:	n/a
28	chr4:10459352-10459402	NHDF-neo	bronchial:	n/a
29	chr4:10459219-10459269	SAEC	small airway:	n/a
30	chr4:10458531-10458581	MCF10A-Er-Src	breast:	n/a
31	chr4:10458049-10458099	ProgFib	skin:	n/a
32	chr4:10460009-10460059	SK-N-MC	brain:	n/a
33	chr4:10459836-10459886	HAEpiC	amniotic membrane:	n/a
34	chr4:10443264-10443314	ovcar-3	ovarian:	n/a
35	chr4:10460237-10460287	H1-hESC	embryonic stem cell:	embryo
36	chr4:10463620-10463670	HepG2	liver:	n/a
37	chr4:10463256-10463306	AG04450	lung:	fetal
38	chr4:10463256-10463306	GM12878	blood:	n/a
39	chr4:10462849-10462899	AG10803	skin:	n/a
40	chr4:10459128-10459178	H1-hESC	embryonic stem cell:	embryo
41	chr4:10459352-10459402	GM12892	blood:	n/a
42	chr4:10458918-10458968	HRPEpiC	eye:	n/a
43	chr4:10463256-10463306	HCM	heart:	n/a
44	chr4:10462849-10462899	HEEpiC	esophagus:	n/a
45	chr4:10459219-10459269	CMK	blood:	n/a
46	chr4:10458918-10458968	ovcar-3	ovarian:	n/a
47	chr4:10463749-10463799	SKMC	muscle:	n/a
48	chr4:10463350-10463400	HRE	kidney:	n/a
49	chr4:10463350-10463400	NHDF-neo	bronchial:	n/a
50	chr4:10463590-10463640	Hepatocyte	liver:	n/a

(count:217 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr4:10187220..10189194-chr4:10403510..10406450,3	K562	blood:
2	chr4:10186739..10189194-chr4:10403510..10406450,4	K562	blood:
3	chr4:10431804..10434625-chr4:10441827..10447697,5	K562	blood:
4	chr4:10226621..10229156-chr4:10309809..10312332,2	K562	blood:
5	chr4:10327845..10330613-chr4:10374388..10375996,2	K562	blood:
6	chr4:10329242..10331797-chr4:10359863..10361623,2	K562	blood:
7	chr4:10104180..10106384-chr4:10453224..10455811,2	K562	blood:
8	chr4:10335172..10337427-chr4:10343892..10346196,2	K562	blood:
9	chr4:10289644..10291282-chr4:10323806..10326517,2	K562	blood:
10	chr4:10182377..10184143-chr4:10453503..10455042,2	K562	blood:
11	chr4:10301025..10303713-chr4:10304138..10305960,2	K562	blood:
12	chr4:10364753..10366272-chr4:10370398..10372088,2	K562	blood:
13	chr4:10483820..10485837-chr4:10490038..10492249,2	K562	blood:
14	chr4:10489847..10492535-chr4:10493316..10495674,3	K562	blood:
15	chr4:10335054..10336642-chr4:10451338..10453609,2	K562	blood:
16	chr4:10327845..10330613-chr4:10374388..10375996,2	K562	blood:
17	chr4:10303834..10305662-chr4:10370006..10372655,2	K562	blood:
18	chr4:10406734..10408445-chr4:10443381..10446084,2	K562	blood:
19	chr4:10119978..10123045-chr4:10320529..10323793,3	K562	blood:
20	chr4:10181802..10184742-chr4:10401642..10403855,2	K562	blood:
21	chr4:10413005..10416502-chr4:10417554..10421094,3	K562	blood:
22	chr4:10242448..10244811-chr4:10340269..10342798,2	K562	blood:
23	chr4:10362193..10364438-chr4:10456296..10459241,2	K562	blood:
24	chr4:10122860..10124582-chr4:10454402..10456296,2	K562	blood:
25	chr4:10483820..10485837-chr4:10490038..10492249,2	K562	blood:
26	chr4:10419551..10421094-chr4:10421815..10424714,2	K562	blood:
27	chr4:10142152..10144542-chr4:10456013..10458159,2	K562	blood:
28	chr4:10354223..10360652-chr4:10361257..10369062,7	K562	blood:
29	chr4:10313155..10314762-chr4:10457693..10459658,2	K562	blood:
30	chr4:10351809..10354070-chr4:10359322..10360898,2	K562	blood:
31	chr4:10312898..10315516-chr4:10318323..10320073,4	K562	blood:
32	chr4:10116151..10120402-chr4:10440722..10445122,4	K562	blood:
33	chr4:10306958..10308632-chr4:10319609..10321643,2	K562	blood:
34	chr4:10331837..10333791-chr4:10338261..10340215,2	K562	blood:
35	chr4:10329017..10330933-chr4:10334130..10336518,2	K562	blood:
36	chr4:10117610..10120083-chr4:10329789..10331862,2	K562	blood:
37	chr4:10183994..10188822-chr4:10326557..10329780,4	K562	blood:
38	chr4:10346965..10350105-chr4:10350832..10355022,4	K562	blood:
39	chr4:10354223..10360652-chr4:10361257..10369062,7	K562	blood:
40	chr4:10489847..10492535-chr4:10493316..10497082,4	K562	blood:
41	chr4:10326554..10329109-chr4:10347770..10349654,2	K562	blood:
42	chr4:10187984..10188890-chr4:10405320..10406071,3	MCF-7	breast:
43	chr4:10344224..10346031-chr4:10349047..10351434,2	K562	blood:
44	chr4:10370932..10373880-chr4:10390683..10392321,2	K562	blood:
45	chr4:10431534..10433490-chr4:10437300..10439063,2	K562	blood:
46	chr4:10406734..10408445-chr4:10443381..10446084,2	K562	blood:
47	chr4:10180991..10184001-chr4:10327240..10329402,3	K562	blood:
48	chr4:10158010..10160333-chr4:10437817..10440737,2	K562	blood:
49	chr4:10326554..10329109-chr4:10347770..10349654,2	K562	blood:
50	chr4:10441301..10442802-chr4:10444428..10446278,2	K562	blood:

(count:23 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DRD5-18	chr4:10369809-10369975	l_2604_chr4:10348296-10419642_testes
2	lnc-CLNK-2	chr4:10458941-10459032	NONHSAT095501
3	lnc-DRD5-18	chr4:10352660-10352812	l_2604_chr4:10348296-10419642_testes
4	lnc-ZNF518B-1	chr4:10433041-10433567	NONHSAT095498
5	lnc-DRD5-18	chr4:10359894-10360314	l_2604_chr4:10348296-10419642_testes
6	lnc-CLNK-1	chr4:10480148-10480547	NONHSAT095504
7	lnc-DRD5-18	chr4:10419449-10419642	l_2604_chr4:10348296-10419642_testes
8	lnc-DRD5-20	chr4:10436252-10437668	NONHSAT095499
9	lnc-DRD5-4	chr4:10404495-10404649	FPKM1_group_22843_transcript_2
10	lnc-DRD5-4	chr4:10404495-10404649	NONHSAT095495
11	lnc-DRD5-18	chr4:10348297-10348499	l_2604_chr4:10348296-10419642_testes
12	lnc-DRD5-4	chr4:10409553-10410132	NONHSAT095495
13	lnc-CLNK-2	chr4:10452511-10454646	NONHSAT095501
14	lnc-CLNK-2	chr4:10458941-10459034	NONHSAT095502
15	lnc-DRD5-21	chr4:10486610-10487079	NONHSAT095505
16	lnc-CLNK-2	chr4:10452511-10456612	NONHSAT095502
17	lnc-CLNK-2	chr4:10456218-10456612	NONHSAT095501
18	lnc-CLNK-2	chr4:10452511-10456612	NONHSAT095503
19	lnc-DRD5-20	chr4:10439848-10440173	NONHSAT095499
20	lnc-DRD5-4	chr4:10409553-10409610	FPKM1_group_22843_transcript_2
21	lnc-DRD5-19	chr4:10437730-10438054	NONHSAT095500
22	lnc-DRD5-18	chr4:10348828-10349271	l_2604_chr4:10348296-10419642_testes
23	lnc-CLNK-2	chr4:10458758-10458800	NONHSAT095503

No data

Variant related genes	Relation type
ENSG00000251338	TF binding region
ENSG00000250613	TF binding region
ENSG00000248419	TF binding region
ZNF518B	TF binding region
ENSG00000251338	CpG island
ENSG00000250613	CpG island
ENSG00000248419	CpG island
ZNF518B	CpG island
ENSG00000071127	chromatin interactions
ENSG00000251338	chromatin interactions
ENSG00000141140	chromatin interactions
ENSG00000250074	chromatin interactions
ENSG00000178163	chromatin interactions
ENSG00000248419	chromatin interactions
ENSG00000250505	chromatin interactions
ENSG00000184886	chromatin interactions
ENSG00000248777	chromatin interactions
ENSG00000251278	chromatin interactions
ENSG00000251296	chromatin interactions
ENSG00000223086	chromatin interactions
ENSG00000250613	chromatin interactions

Extended variants
information (count: 9522 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:9522 , 50 per page) page: 1 2 3 4 5 6 7 ... 191

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529538397	chr4:10300238-10300239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs73224416	chr4:10300241-10300242	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs77213916	chr4:10300279-10300280	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs553172836	chr4:10300286-10300287	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs574850486	chr4:10300313-10300314	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs11732729	chr4:10300316-10300317	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs539818333	chr4:10300317-10300318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs190628336	chr4:10300320-10300321	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs2080077	chr4:10300382-10300383	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs2098237	chr4:10300442-10300443	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs555493329	chr4:10300458-10300459	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs573754846	chr4:10300462-10300463	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs182804288	chr4:10300468-10300469	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs2098236	chr4:10300472-10300473	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs199652870	chr4:10300473-10300474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs187274113	chr4:10300485-10300486	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs544577773	chr4:10300496-10300497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs564080193	chr4:10300507-10300508	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs559733927	chr4:10300526-10300527	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs149649814	chr4:10300538-10300539	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs572488823	chr4:10300561-10300562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs144231798	chr4:10300596-10300597	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs561078174	chr4:10300606-10300607	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs529449684	chr4:10300647-10300648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs551180071	chr4:10300660-10300661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs112056466	chr4:10300665-10300666	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs533681319	chr4:10300703-10300704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs142304378	chr4:10300710-10300711	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs566877318	chr4:10300727-10300728	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs192736048	chr4:10300750-10300751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs117141830	chr4:10300753-10300754	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs183076571	chr4:10300759-10300760	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs531744401	chr4:10300769-10300770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs147483495	chr4:10300785-10300786	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs6834574	chr4:10300814-10300815	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs571175627	chr4:10300817-10300818	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs10939829	chr4:10300819-10300820	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs563857128	chr4:10300821-10300822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs187774359	chr4:10300830-10300831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs192694039	chr4:10300836-10300837	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs185696835	chr4:10300854-10300855	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs554343190	chr4:10300864-10300865	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs189388963	chr4:10300882-10300883	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs544443328	chr4:10300924-10300925	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs563104135	chr4:10300927-10300928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs533622334	chr4:10300956-10300957	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs545713940	chr4:10300959-10300960	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs199509711	chr4:10300961-10300962	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs74272220	chr4:10300966-10300967	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs398063270	chr4:10300976-10300977	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Neuroblastoma	20406844	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2016 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:10298800-10300400	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr4:10298800-10300400	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr4:10298800-10300600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr4:10298800-10301000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr4:10299000-10300400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr4:10299000-10300800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr4:10299000-10300800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr4:10299000-10301000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr4:10299000-10301000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr4:10299000-10301200	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr4:10299000-10303400	Weak transcription	HMEC	breast
12	chr4:10299000-10303600	Weak transcription	NHEK	skin
13	chr4:10299000-10304800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr4:10299400-10301400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr4:10299400-10302000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr4:10299600-10300400	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr4:10299600-10300800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr4:10299600-10306800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr4:10299800-10301200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr4:10299800-10305400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr4:10300200-10300400	Enhancers	Brain Hippocampus Middle	brain
22	chr4:10300200-10301200	Enhancers	Placenta	Placenta
23	chr4:10300400-10300800	Enhancers	H1 Cell Line	embryonic stem cell
24	chr4:10300400-10300800	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr4:10300400-10301200	Enhancers	H9 Cell Line	embryonic stem cell
26	chr4:10300400-10301600	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr4:10300600-10301400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr4:10300800-10301400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr4:10300800-10301600	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr4:10300800-10301800	Weak transcription	H1 Cell Line	embryonic stem cell
31	chr4:10300800-10301800	Weak transcription	HUES64 Cell Line	embryonic stem cell
32	chr4:10301000-10301200	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr4:10301000-10301600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr4:10301000-10302200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr4:10301000-10303800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr4:10301200-10304000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr4:10301200-10304000	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr4:10301200-10304000	Weak transcription	Placenta	Placenta
39	chr4:10301400-10301800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr4:10301400-10303400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr4:10301600-10302600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr4:10301600-10302600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
43	chr4:10301600-10303800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr4:10301800-10302000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr4:10301800-10303000	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr4:10302000-10302200	Enhancers	H1 Cell Line	embryonic stem cell
47	chr4:10302000-10302200	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr4:10302000-10305800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr4:10302200-10302600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
50	chr4:10302200-10303400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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