Variant report

Variant	nsv830029
Chromosome Location	chr4:107203096-107353483
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1739)
CpG islands
(count:1223)
Chromatin interactive
region (count:61)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1739 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:107286679-107287176	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:107224851-107225233	K562	blood:	n/a	n/a
3	ARID3A	chr4:107236935-107238209	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:107265521-107265852	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:107250191-107250363	K562	blood:	n/a	n/a
6	ARID3A	chr4:107343316-107343362	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:107254297-107254694	HepG2	liver:	n/a	n/a
8	ARID3A	chr4:107240223-107240253	HepG2	liver:	n/a	n/a
9	ARID3A	chr4:107290661-107290836	HepG2	liver:	n/a	n/a
10	ARID3A	chr4:107234380-107234799	HepG2	liver:	n/a	n/a
11	ARID3A	chr4:107290660-107290984	K562	blood:	n/a	n/a
12	ARID3A	chr4:107208155-107209087	HepG2	liver:	n/a	n/a
13	ATF1	chr4:107286804-107287045	K562	blood:	n/a	n/a
14	ATF1	chr4:107236740-107238091	K562	blood:	n/a	n/a
15	ATF2	chr4:107237195-107237980	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr4:107237040-107238074	GM12878	blood:	n/a	n/a
17	ATF2	chr4:107237261-107238038	GM12878	blood:	n/a	n/a
18	ATF2	chr4:107237102-107237989	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF3	chr4:107237169-107237603	A549	lung:	n/a	chr4:107237306-107237314
20	ATF3	chr4:107237243-107237804	K562	blood:	n/a	chr4:107237306-107237314
21	ATF3	chr4:107237200-107237728	H1-hESC	embryonic stem cell:	n/a	chr4:107237306-107237314
22	ATF3	chr4:107237198-107237880	GM12878	blood:	n/a	chr4:107237306-107237314
23	BACH1	chr4:107208566-107208766	K562	blood:	n/a	n/a
24	BACH1	chr4:107312398-107312411	K562	blood:	n/a	n/a
25	BACH1	chr4:107236955-107237132	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr4:107236325-107236349	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr4:107236816-107237016	K562	blood:	n/a	n/a
28	BCL3	chr4:107237245-107237821	A549	lung:	n/a	n/a
29	BCL3	chr4:107237087-107237869	A549	lung:	n/a	n/a
30	BCLAF1	chr4:107236610-107238013	GM12878	blood:	n/a	n/a
31	BCLAF1	chr4:107236774-107237953	GM12878	blood:	n/a	n/a
32	BHLHE40	chr4:107234336-107234585	HepG2	liver:	n/a	n/a
33	BHLHE40	chr4:107273046-107273193	GM12878	blood:	n/a	n/a
34	BHLHE40	chr4:107236263-107238635	K562	blood:	n/a	chr4:107237160-107237176
35	BHLHE40	chr4:107268732-107268860	K562	blood:	n/a	n/a
36	BHLHE40	chr4:107243118-107243318	K562	blood:	n/a	n/a
37	BHLHE40	chr4:107208489-107208936	HepG2	liver:	n/a	n/a
38	BHLHE40	chr4:107234291-107234938	K562	blood:	n/a	n/a
39	BHLHE40	chr4:107237099-107238030	HepG2	liver:	n/a	chr4:107237160-107237176
40	BHLHE40	chr4:107234293-107234627	GM12878	blood:	n/a	n/a
41	BHLHE40	chr4:107250345-107250604	K562	blood:	n/a	n/a
42	BHLHE40	chr4:107236945-107238657	GM12878	blood:	n/a	chr4:107237160-107237176
43	BRCA1	chr4:107236757-107236957	HepG2	liver:	n/a	n/a
44	BRCA1	chr4:107237136-107238059	H1-hESC	embryonic stem cell:	n/a	n/a
45	BRCA1	chr4:107237242-107237930	HepG2	liver:	n/a	n/a
46	BRCA1	chr4:107237177-107237878	Hela-S3	cervix:	n/a	n/a
47	CBX3	chr4:107236972-107238087	K562	blood:	n/a	n/a
48	CBX3	chr4:107316829-107317067	K562	blood:	n/a	n/a
49	CBX3	chr4:107316724-107317113	HCT-116	colon:	n/a	n/a
50	CBX3	chr4:107290594-107290983	HCT-116	colon:	n/a	n/a

(count:1223 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:107238104-107238154	NH-A	brain:	n/a
2	chr4:107208133-107208183	U87	brain:	n/a
3	chr4:107238002-107238052	PANC-1	pancreas:	n/a
4	chr4:107238104-107238154	NH-A	brain:	n/a
5	chr4:107208133-107208183	U87	brain:	n/a
6	chr4:107238002-107238052	PANC-1	pancreas:	n/a
7	chr4:107208133-107208183	PrEC	prostate:	n/a
8	chr4:107269030-107269080	GM12891	blood:	n/a
9	chr4:107237940-107237990	Hela-S3	cervix:	n/a
10	chr4:107237686-107237736	AoSMC	blood vessel:	n/a
11	chr4:107258035-107258085	SK-N-MC	brain:	n/a
12	chr4:107258035-107258085	HRE	kidney:	n/a
13	chr4:107269030-107269080	HEEpiC	esophagus:	n/a
14	chr4:107237727-107237777	AG10803	skin:	n/a
15	chr4:107208133-107208183	GM12892	blood:	n/a
16	chr4:107238125-107238175	SK-N-SH_RA	brain:	n/a
17	chr4:107237727-107237777	NB4	blood:	n/a
18	chr4:107258035-107258085	Hepatocyte	liver:	n/a
19	chr4:107208133-107208183	HNPCEpiC	eye:	n/a
20	chr4:107242537-107242587	T-47D	breast:	n/a
21	chr4:107269030-107269080	HRPEpiC	eye:	n/a
22	chr4:107224533-107224583	PANC-1	pancreas:	n/a
23	chr4:107237488-107237538	AG09319	gingival:	n/a
24	chr4:107242537-107242587	HRE	kidney:	n/a
25	chr4:107237991-107238041	BE2_C	brain:	n/a
26	chr4:107237727-107237777	BJ	skin:	n/a
27	chr4:107242537-107242587	NH-A	brain:	n/a
28	chr4:107237488-107237538	HRPEpiC	eye:	n/a
29	chr4:107238002-107238052	AG10803	skin:	n/a
30	chr4:107238104-107238154	HCT-116	colon:	n/a
31	chr4:107242537-107242587	GM12892	blood:	n/a
32	chr4:107258035-107258085	GM06990	blood:	n/a
33	chr4:107237686-107237736	NH-A	brain:	n/a
34	chr4:107238002-107238052	AG09309	skin:	n/a
35	chr4:107269030-107269080	GM06990	blood:	n/a
36	chr4:107238104-107238154	ovcar-3	ovarian:	n/a
37	chr4:107237183-107237233	CMK	blood:	n/a
38	chr4:107238104-107238154	HRE	kidney:	n/a
39	chr4:107237183-107237233	BJ	skin:	n/a
40	chr4:107238104-107238154	HepG2	liver:	n/a
41	chr4:107237183-107237233	AG09309	skin:	n/a
42	chr4:107237991-107238041	A549	lung:	n/a
43	chr4:107237688-107237738	H1-hESC	embryonic stem cell:	embryo
44	chr4:107223505-107223555	HRPEpiC	eye:	n/a
45	chr4:107237870-107237920	GM12891	blood:	n/a
46	chr4:107237940-107237990	HRPEpiC	eye:	n/a
47	chr4:107208133-107208183	HRPEpiC	eye:	n/a
48	chr4:107223505-107223555	GM12892	blood:	n/a
49	chr4:107238104-107238154	PFSK-1	brain:	n/a
50	chr4:107237870-107237920	HNPCEpiC	eye:	n/a

(count:61 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:107187038..107188038-chr4:107249952..107250600,3	MCF-7	breast:
2	chr4:107235692..107241045-chr4:107249153..107254463,7	K562	blood:
3	chr4:107238766..107241197-chr4:107243663..107246436,3	MCF-7	breast:
4	chr4:107251770..107254380-chr4:107254601..107256779,2	MCF-7	breast:
5	chr4:107217078..107218792-chr4:107237509..107239809,2	K562	blood:
6	chr4:107255973..107258008-chr4:107260833..107262354,2	K562	blood:
7	chr4:107218591..107221173-chr4:107222816..107224928,3	K562	blood:
8	chr4:107258354..107261291-chr4:107264865..107267295,3	K562	blood:
9	chr4:107243946..107245943-chr4:107262663..107264283,2	K562	blood:
10	chr4:107238261..107242846-chr4:107256432..107259782,4	K562	blood:
11	chr4:107258354..107261291-chr4:107264865..107267295,3	K562	blood:
12	chr4:107226289..107231817-chr4:107234990..107238909,9	MCF-7	breast:
13	chr4:107246333..107250100-chr4:107250113..107253546,4	K562	blood:
14	chr4:107237104..107239222-chr4:107242946..107245918,2	MCF-7	breast:
15	chr4:107349397..107350031-chr4:107362531..107363489,2	MCF-7	breast:
16	chr4:107235080..107237825-chr4:107304121..107307055,2	K562	blood:
17	chr4:107237524..107239037-chr4:107241153..107242940,2	MCF-7	breast:
18	chr4:107290301..107292526-chr4:107422827..107424058,19	MCF-7	breast:
19	chr20:57463851..57464376-chr4:107236670..107237605,2	Hela-S3	cervix:
20	chr4:107288668..107290808-chr4:107293759..107296062,2	K562	blood:
21	chr4:107288592..107289255-chr4:107423410..107423938,2	MCF-7	breast:
22	chr4:107288668..107290808-chr4:107293759..107296062,2	K562	blood:
23	chr4:107226289..107231817-chr4:107234990..107238909,9	MCF-7	breast:
24	chr4:107250428..107252000-chr4:107255432..107258079,2	K562	blood:
25	chr4:107238766..107241197-chr4:107243663..107246436,3	MCF-7	breast:
26	chr4:107287024..107287560-chr5:153670760..153671260,2	Hela-S3	cervix:
27	chr4:107243946..107245943-chr4:107262663..107264283,2	K562	blood:
28	chr4:107250428..107252000-chr4:107255432..107258079,2	K562	blood:
29	chr4:107335618..107338970-chr4:107353446..107357718,3	K562	blood:
30	chr4:107237852..107239774-chr4:107248224..107252167,3	K562	blood:
31	chr4:107275880..107279456-chr4:107281523..107285039,4	K562	blood:
32	chr4:107216359..107217869-chr4:107220445..107222881,2	K562	blood:
33	chr4:107237734..107238393-chr9:33167089..33167643,2	NB4	blood:
34	chr4:107246333..107250100-chr4:107250113..107253546,3	K562	blood:
35	chr4:107290453..107290976-chr4:107421149..107422009,2	MCF-7	breast:
36	chr4:107290348..107291609-chr4:107422851..107424531,10	MCF-7	breast:
37	chr4:100869528..100871186-chr4:107235611..107237116,2	K562	blood:
38	chr4:107237524..107239037-chr4:107241153..107242940,2	MCF-7	breast:
39	chr4:107215261..107218209-chr4:107235780..107238587,4	MCF-7	breast:
40	chr4:107303398..107305509-chr4:107317461..107319625,2	K562	blood:
41	chr4:107243504..107246800-chr4:107249107..107253056,3	MCF-7	breast:
42	chr4:107250318..107251249-chr4:107730056..107730667,2	MCF-7	breast:
43	chr4:107290770..107291311-chr4:107424769..107425646,2	MCF-7	breast:
44	chr4:107275880..107279456-chr4:107281523..107285039,4	K562	blood:
45	chr4:107224095..107225735-chr4:107236744..107238775,2	MCF-7	breast:
46	chr4:107251770..107254380-chr4:107254601..107256779,2	MCF-7	breast:
47	chr4:107243504..107246800-chr4:107249107..107253056,3	MCF-7	breast:
48	chr4:107235907..107237713-chr4:107263142..107264645,2	MCF-7	breast:
49	chr4:107216359..107217869-chr4:107220445..107222881,2	K562	blood:
50	chr11:62608849..62609649-chr4:107237489..107238158,2	Hela-S3	cervix:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	AIMP1	hsa-miR-155-5p	chr4:107270060-107270081

Variant related genes	Relation type
ENSG00000222333	TF binding region
ENSG00000249613	TF binding region
GIMD1	TF binding region
AIMP1	TF binding region
TBCK	TF binding region
ENSG00000222333	CpG island
ENSG00000249613	CpG island
GIMD1	CpG island
AIMP1	CpG island
TBCK	CpG island
ENSG00000164022	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000086062	chromatin interactions
ENSG00000087460	chromatin interactions
ENSG00000249613	chromatin interactions
ENSG00000222333	chromatin interactions
ENSG00000145348	chromatin interactions
ENSG00000225806	chromatin interactions
ENSG00000245322	chromatin interactions

Extended variants
information (count: 4246 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:4246 , 50 per page) page: 1 2 3 4 5 6 7 ... 85

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375290567	chr4:107203125-107203126	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs575281738	chr4:107203135-107203136	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs7697996	chr4:107203162-107203163	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs191096396	chr4:107203185-107203186	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs547868007	chr4:107203237-107203238	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs575126504	chr4:107203258-107203259	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs116772041	chr4:107203361-107203362	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs72876587	chr4:107203449-107203450	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs76529937	chr4:107203492-107203493	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs60306673	chr4:107203583-107203584	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs149047285	chr4:107203632-107203633	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs562645667	chr4:107203649-107203650	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs531567132	chr4:107203656-107203657	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs549436331	chr4:107203662-107203663	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs542248961	chr4:107203686-107203687	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs371103664	chr4:107203800-107203801	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs561021392	chr4:107203859-107203860	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs142120285	chr4:107203940-107203941	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs375466895	chr4:107203972-107203973	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs546460970	chr4:107204037-107204038	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs566634254	chr4:107204038-107204039	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs532366047	chr4:107204057-107204058	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs552252613	chr4:107204080-107204081	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs183284289	chr4:107204142-107204143	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs559529727	chr4:107204147-107204148	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs147822314	chr4:107204183-107204184	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs537442761	chr4:107204201-107204202	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs554579247	chr4:107204239-107204240	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs141386963	chr4:107204254-107204255	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs113921133	chr4:107204290-107204291	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs534472869	chr4:107204373-107204374	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs554067507	chr4:107204378-107204379	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs576978004	chr4:107204385-107204386	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs370454993	chr4:107204441-107204442	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs72876590	chr4:107204499-107204500	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs3113246	chr4:107204538-107204539	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs544324461	chr4:107204574-107204575	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs571074620	chr4:107204657-107204658	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs57146559	chr4:107204681-107204682	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs541834439	chr4:107204697-107204698	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs562145612	chr4:107204744-107204745	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs72876592	chr4:107204776-107204777	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs540503256	chr4:107204814-107204815	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs531199669	chr4:107204818-107204819	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs560465645	chr4:107204850-107204851	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs552527576	chr4:107204854-107204855	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs571001325	chr4:107204868-107204869	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs536813214	chr4:107204910-107204911	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs138227499	chr4:107204914-107204915	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs552449256	chr4:107204915-107204916	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Melanoma	20688739	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	18000384	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
myeloid cancer	21057493	CNVD
Cognitive impairment	21505072	CNVD
Acute myeloid leukemia	21251322	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Chronic lymphocytic leukemia	21215367	CNVD
Cancer	21215367	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2831 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:107114600-107236000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr4:107141600-107214800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr4:107155600-107236000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
4	chr4:107170800-107208200	Weak transcription	Fetal Kidney	kidney
5	chr4:107177400-107207600	Weak transcription	Fetal Brain Female	brain
6	chr4:107177600-107205600	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr4:107177800-107207600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr4:107177800-107207600	Weak transcription	Adipose Nuclei	Adipose
9	chr4:107177800-107211600	Weak transcription	Duodenum Smooth Muscle	Duodenum
10	chr4:107177800-107215200	Weak transcription	Brain Hippocampus Middle	brain
11	chr4:107178000-107205400	Weak transcription	Thymus	Thymus
12	chr4:107178000-107207800	Weak transcription	Primary monocytes fromperipheralblood	blood
13	chr4:107178000-107207800	Weak transcription	Lung	lung
14	chr4:107178000-107207800	Weak transcription	Sigmoid Colon	Sigmoid Colon
15	chr4:107178000-107208200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
16	chr4:107178000-107208400	Weak transcription	Primary T cells fromperipheralblood	blood
17	chr4:107178000-107211800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
18	chr4:107178000-107211800	Weak transcription	Fetal Muscle Trunk	muscle
19	chr4:107178000-107211800	Weak transcription	Fetal Muscle Leg	muscle
20	chr4:107178000-107211800	Weak transcription	Fetal Stomach	stomach
21	chr4:107178000-107211800	Weak transcription	Left Ventricle	heart
22	chr4:107178000-107211800	Weak transcription	Ovary	ovary
23	chr4:107178000-107236200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr4:107178000-107236200	Weak transcription	Right Ventricle	heart
25	chr4:107178000-107236600	Weak transcription	Esophagus	oesophagus
26	chr4:107178000-107236600	Weak transcription	Pancreas	Pancrea
27	chr4:107178200-107211600	Weak transcription	Placenta	Placenta
28	chr4:107178200-107236000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
29	chr4:107179000-107211400	Weak transcription	Primary B cells from peripheral blood	blood
30	chr4:107179800-107208600	Weak transcription	Primary T helper cells fromperipheralblood	blood
31	chr4:107180600-107207000	Weak transcription	Monocytes-CD14+_RO01746	blood
32	chr4:107180600-107207400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
33	chr4:107182800-107203600	Weak transcription	HSMM	muscle
34	chr4:107186000-107211800	Weak transcription	Rectal Mucosa Donor 31	rectum
35	chr4:107186200-107207600	Weak transcription	Liver	Liver
36	chr4:107186200-107207800	Weak transcription	Rectal Mucosa Donor 29	rectum
37	chr4:107186200-107212800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr4:107187000-107208200	Weak transcription	Fetal Intestine Large	intestine
39	chr4:107187600-107215200	Weak transcription	Fetal Intestine Small	intestine
40	chr4:107190800-107208600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr4:107192000-107208600	Weak transcription	HSMMtube	muscle
42	chr4:107192400-107215200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
43	chr4:107192600-107208000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr4:107193000-107204400	Weak transcription	HepG2	liver
45	chr4:107194000-107207600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr4:107194200-107211800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr4:107194400-107221200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr4:107194800-107227600	Weak transcription	Brain Angular Gyrus	brain
49	chr4:107195000-107203800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr4:107195000-107207800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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